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Publications indexed to the term Chromosome Mapping

FacultyTitle
2The Year of the Rat: The Rat Genome Database at 20: a multi-species knowledgebase and analysis platform. (Smith JR, Hayman GT, Wang SJ, Laulederkind SJF, Hoffman MJ, Kaldunski ML, Tutaj M, Thota J, Nalabolu HS, Ellanki SLR, Tutaj MA, De Pons JL, Kwitek AE, Dwinell MR, Shimoyama ME) Nucleic Acids Res 2020 01 08;48(D1):D731-D742       4 Citations
2Mapping Mammary Tumor Traits in the Rat. (Flister MJ, Joshi A, Bergom C, Rui H) Methods Mol Biol 2019;2018:249-267    
2Identification of a Rat Mammary Tumor Risk Locus That Is Syntenic with the Commonly Amplified 8q12.1 and 8q22.1 Regions in Human Breast Cancer Patients. (Plasterer C, Tsaih SW, Lemke A, Schilling R, Dwinell M, Rau A, Auer P, Rui H, Flister MJ) G3 (Bethesda) 2019 05 07;9(5):1739-1743       2 Citations
4Mapping genetic modifiers of radiation-induced cardiotoxicity to rat chromosome 3. (Schlaak RA, Frei A, Schottstaedt AM, Tsaih SW, Fish BL, Harmann L, Liu Q, Gasperetti T, Medhora M, North PE, Strande JL, Sun Y, Rui H, Flister MJ, Bergom C) Am J Physiol Heart Circ Physiol 2019 06 01;316(6):H1267-H1280       5 Citations
1Real-Time Targeted Genome Profile Analysis of Pancreatic Ductal Adenocarcinomas Identifies Genetic Alterations That Might Be Targeted With Existing Drugs or Used as Biomarkers. (Singhi AD, George B, Greenbowe JR, Chung J, Suh J, Maitra A, Klempner SJ, Hendifar A, Milind JM, Golan T, Brand RE, Zureikat AH, Roy S, Schrock AB, Miller VA, Ross JS, Ali SM, Bahary N) Gastroenterology 2019 06;156(8):2242-2253.e4       22 Citations
4Genome-wide map of proximity linkage to renin proximal promoter in rat. (Stodola TJ, Liu P, Liu Y, Vallejos AK, Geurts AM, Greene AS, Liang M) Physiol Genomics 2018 05 01;50(5):323-331       4 Citations
1The complex genetics of hypoplastic left heart syndrome. (Liu X, Yagi H, Saeed S, Bais AS, Gabriel GC, Chen Z, Peterson KA, Li Y, Schwartz MC, Reynolds WT, Saydmohammed M, Gibbs B, Wu Y, Devine W, Chatterjee B, Klena NT, Kostka D, de Mesy Bentley KL, Ganapathiraju MK, Dexheimer P, Leatherbury L, Khalifa O, Bhagat A, Zahid M, Pu W, Watkins S, Grossfeld P, Murray SA, Porter GA Jr, Tsang M, Martin LJ, Benson DW, Aronow BJ, Lo CW) Nat Genet 2017 Jul;49(7):1152-1159       51 Citations
1Fine mapping of chromosome 5p15.33 identifies novel lung cancer susceptibility loci in Han Chinese. (Dong J, Cheng Y, Zhu M, Wen Y, Wang C, Wang Y, Geng L, Shen W, Liu J, Li Z, Zhang J, Ma H, Dai J, Jin G, Hu Z, Shen H) Int J Cancer 2017 08 01;141(3):447-456       7 Citations
1Congenic mapping identifies a novel Idd9 subregion regulating type 1 diabetes in NOD mice. (Lin B, Ciecko AE, MacKinney E, Serreze DV, Chen YG) Immunogenetics 2017 03;69(3):193-198       2 Citations
1Association of a Chromosomal Rearrangement Event with Mouse Posterior Polymorphous Corneal Dystrophy and Alterations in Csrp2bp, Dzank1, and Ovol2 Gene Expression. (Shen AL, Moran SA, Glover EA, Drinkwater NR, Swearingen RE, Teixeira LB, Bradfield CA) PLoS One 2016;11(6):e0157577       3 Citations
1Association mapping by pooled sequencing identifies TOLL 11 as a protective factor against Plasmodium falciparum in Anopheles gambiae. (Redmond SN, Eiglmeier K, Mitri C, Markianos K, Guelbeogo WM, Gneme A, Isaacs AT, Coulibaly B, Brito-Fravallo E, Maslen G, Mead D, Niare O, Traore SF, Sagnon N, Kwiatkowski D, Riehle MM, Vernick KD) BMC Genomics 2015 Oct 13;16:779       9 Citations
1Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers. (Onengut-Gumuscu S, Chen WM, Burren O, Cooper NJ, Quinlan AR, Mychaleckyj JC, Farber E, Bonnie JK, Szpak M, Schofield E, Achuthan P, Guo H, Fortune MD, Stevens H, Walker NM, Ward LD, Kundaje A, Kellis M, Daly MJ, Barrett JC, Cooper JD, Deloukas P, Type 1 Diabetes Genetics Consortium, Todd JA, Wallace C, Concannon P, Rich SS) Nat Genet 2015 Apr;47(4):381-6       249 Citations
1A locus on mouse chromosome 13 inversely regulates CD1d expression and the development of invariant natural killer T-cells. (Tsaih SW, Presa M, Khaja S, Ciecko AE, Serreze DV, Chen YG) Genes Immun 2015 Apr-May;16(3):221-30       2 Citations
1Genome analysis of a major urban malaria vector mosquito, Anopheles stephensi. (Jiang X, Peery A, Hall AB, Sharma A, Chen XG, Waterhouse RM, Komissarov A, Riehle MM, Shouche Y, Sharakhova MV, Lawson D, Pakpour N, Arensburger P, Davidson VL, Eiglmeier K, Emrich S, George P, Kennedy RC, Mane SP, Maslen G, Oringanje C, Qi Y, Settlage R, Tojo M, Tubio JM, Unger MF, Wang B, Vernick KD, Ribeiro JM, James AA, Michel K, Riehle MA, Luckhart S, Sharakhov IV, Tu Z) Genome Biol 2014 Sep 23;15(9):459       58 Citations
1TNNI3K mutation in familial syndrome of conduction system disease, atrial tachyarrhythmia and dilated cardiomyopathy. (Theis JL, Zimmermann MT, Larsen BT, Rybakova IN, Long PA, Evans JM, Middha S, de Andrade M, Moss RL, Wieben ED, Michels VV, Olson TM) Hum Mol Genet 2014 Nov 01;23(21):5793-804       20 Citations
1Genomic structure of nucleotide diversity among Lyon rat models of metabolic syndrome. (Ma MC, Atanur SS, Aitman TJ, Kwitek AE) BMC Genomics 2014 Mar 14;15:197       6 Citations
1Collateral development: the quest continues. (Lohr NL) Circ Res 2014 Feb 14;114(4):591-3       2 Citations
1A graph-theoretical approach to the selection of the minimum tiling path from a physical map. (Bozdag S, Close TJ, Lonardi S) IEEE/ACM Trans Comput Biol Bioinform 2013 Mar-Apr;10(2):352-60       5 Citations
2Characterization of human plasma-derived exosomal RNAs by deep sequencing. (Huang X, Yuan T, Tschannen M, Sun Z, Jacob H, Du M, Liang M, Dittmar RL, Liu Y, Liang M, Kohli M, Thibodeau SN, Boardman L, Wang L) BMC Genomics 2013 May 10;14:319       477 Citations
1Functional genomic assessment of phosgene-induced acute lung injury in mice. (Leikauf GD, Concel VJ, Bein K, Liu P, Berndt A, Martin TM, Ganguly K, Jang AS, Brant KA, Dopico RA Jr, Upadhyay S, Cario C, Di YP, Vuga LJ, Kostem E, Eskin E, You M, Kaminski N, Prows DR, Knoell DL, Fabisiak JP) Am J Respir Cell Mol Biol 2013 Sep;49(3):368-83       14 Citations
1Loci influencing blood pressure identified using a cardiovascular gene-centric array. (Ganesh SK, Tragante V, Guo W, Guo Y, Lanktree MB, Smith EN, Johnson T, Castillo BA, Barnard J, Baumert J, Chang YP, Elbers CC, Farrall M, Fischer ME, Franceschini N, Gaunt TR, Gho JM, Gieger C, Gong Y, Isaacs A, Kleber ME, Mateo Leach I, McDonough CW, Meijs MF, Mellander O, Molony CM, Nolte IM, Padmanabhan S, Price TS, Rajagopalan R, Shaffer J, Shah S, Shen H, Soranzo N, van der Most PJ, Van Iperen EP, Van Setten J, Vonk JM, Zhang L, Beitelshees AL, Berenson GS, Bhatt DL, Boer JM, Boerwinkle E, Burkley B, Burt A, Chakravarti A, Chen W, Cooper-Dehoff RM, Curtis SP, Dreisbach A, Duggan D, Ehret GB, Fabsitz RR, Fornage M, Fox E, Furlong CE, Gansevoort RT, Hofker MH, Hovingh GK, Kirkland SA, Kottke-Marchant K, Kutlar A, Lacroix AZ, Langaee TY, Li YR, Lin H, Liu K, Maiwald S, Malik R, CARDIOGRAM, METASTROKE, Murugesan G, Newton-Cheh C, O'Connell JR, Onland-Moret NC, Ouwehand WH, Palmas W, Penninx BW, Pepine CJ, Pettinger M, Polak JF, Ramachandran VS, Ranchalis J, Redline S, Ridker PM, Rose LM, Scharnag H, Schork NJ, Shimbo D, Shuldiner AR, Srinivasan SR, Stolk RP, Taylor HA, Thorand B, Trip MD, van Duijn CM, Verschuren WM, Wijmenga C, Winkelmann BR, Wyatt S, Young JH, Boehm BO, Caulfield MJ, Chasman DI, Davidson KW, Doevendans PA, Fitzgerald GA, Gums JG, Hakonarson H, Hillege HL, Illig T, Jarvik GP, Johnson JA, Kastelein JJ, Koenig W, LifeLines Cohort Study, März W, Mitchell BD, Murray SS, Oldehinkel AJ, Rader DJ, Reilly MP, Reiner AP, Schadt EE, Silverstein RL, Snieder H, Stanton AV, Uitterlinden AG, van der Harst P, van der Schouw YT, Samani NJ, Johnson AD, Munroe PB, de Bakker PI, Zhu X, Levy D, Keating BJ, Asselbergs FW) Hum Mol Genet 2013 Apr 15;22(8):1663-78       92 Citations
1Discovery and fine mapping of serum protein loci through transethnic meta-analysis. (Franceschini N, van Rooij FJ, Prins BP, Feitosa MF, Karakas M, Eckfeldt JH, Folsom AR, Kopp J, Vaez A, Andrews JS, Baumert J, Boraska V, Broer L, Hayward C, Ngwa JS, Okada Y, Polasek O, Westra HJ, Wang YA, Del Greco M F, Glazer NL, Kapur K, Kema IP, Lopez LM, Schillert A, Smith AV, Winkler CA, Zgaga L, LifeLines Cohort Study, Bandinelli S, Bergmann S, Boban M, Bochud M, Chen YD, Davies G, Dehghan A, Ding J, Doering A, Durda JP, Ferrucci L, Franco OH, Franke L, Gunjaca G, Hofman A, Hsu FC, Kolcic I, Kraja A, Kubo M, Lackner KJ, Launer L, Loehr LR, Li G, Meisinger C, Nakamura Y, Schwienbacher C, Starr JM, Takahashi A, Torlak V, Uitterlinden AG, Vitart V, Waldenberger M, Wild PS, Kirin M, Zeller T, Zemunik T, Zhang Q, Ziegler A, Blankenberg S, Boerwinkle E, Borecki IB, Campbell H, Deary IJ, Frayling TM, Gieger C, Harris TB, Hicks AA, Koenig W, O' Donnell CJ, Fox CS, Pramstaller PP, Psaty BM, Reiner AP, Rotter JI, Rudan I, Snieder H, Tanaka T, van Duijn CM, Vollenweider P, Waeber G, Wilson JF, Witteman JC, Wolffenbuttel BH, Wright AF, Wu Q, Liu Y, Jenny NS, North KE, Felix JF, Alizadeh BZ, Cupples LA, Perry JR, Morris AP) Am J Hum Genet 2012 Oct 05;91(4):744-53       51 Citations
1Genetic variants in Arhgef11 are associated with kidney injury in the Dahl salt-sensitive rat. (Williams JM, Johnson AC, Stelloh C, Dreisbach AW, Franceschini N, Regner KR, Townsend RR, Roman RJ, Garrett MR) Hypertension 2012 Nov;60(5):1157-68       20 Citations
1Genotype imputation for African Americans using data from HapMap phase II versus 1000 genomes projects. (Sung YJ, Gu CC, Tiwari HK, Arnett DK, Broeckel U, Rao DC) Genet Epidemiol 2012 Jul;36(5):508-16       11 Citations
1Integrative assessment of chlorine-induced acute lung injury in mice. (Leikauf GD, Pope-Varsalona H, Concel VJ, Liu P, Bein K, Berndt A, Martin TM, Ganguly K, Jang AS, Brant KA, Dopico RA Jr, Upadhyay S, Di YP, Li Q, Hu Z, Vuga LJ, Medvedovic M, Kaminski N, You M, Alexander DC, McDunn JE, Prows DR, Knoell DL, Fabisiak JP) Am J Respir Cell Mol Biol 2012 Aug;47(2):234-44       20 Citations
1A 4.1-Mb congenic region of Rf-4 contributes to glomerular permeability. (O'Meara CC, Lutz MM, Sarkis AB, Xu H, Kothinti RK, Hoffman M, Moreno C, Tabatabai NM, Lazar J, Roman RJ, Jacob HJ) J Am Soc Nephrol 2012 May;23(5):825-33       4 Citations
2Genetic mapping of habitual substance use, obesity-related traits, responses to mental and physical stress, and heart rate and blood pressure measurements reveals shared genes that are overrepresented in the neural synapse. (Nikpay M, Šeda O, Tremblay J, Petrovich M, Gaudet D, Kotchen TA, Cowley AW Jr, Hamet P) Hypertens Res 2012 Jun;35(6):585-91       24 Citations
1Genome characterization of the oleaginous fungus Mortierella alpina. (Wang L, Chen W, Feng Y, Ren Y, Gu Z, Chen H, Wang H, Thomas MJ, Zhang B, Berquin IM, Li Y, Wu J, Zhang H, Song Y, Liu X, Norris JS, Wang S, Du P, Shen J, Wang N, Yang Y, Wang W, Feng L, Ratledge C, Zhang H, Chen YQ) PLoS One 2011;6(12):e28319       94 Citations
3Genome-wide association and fine mapping of genetic loci predisposing to colon carcinogenesis in mice. (Liu P, Lu Y, Liu H, Wen W, Jia D, Wang Y, You M) Mol Cancer Res 2012 Jan;10(1):66-74       21 Citations
1On coding genotypes for genetic markers with multiple alleles in genetic association study of quantitative traits. (Wang T) BMC Genet 2011 Sep 21;12:82       6 Citations
1Characterization of a dominant cone degeneration in a green fluorescent protein-reporter mouse with disruption of Loci associated with human dominant retinal dystrophy. (Lipinski DM, Yusuf M, Barnard AR, Damant C, Charbel Issa P, Singh MS, Lee E, Davies WL, Volpi EV, MacLaren RE) Invest Ophthalmol Vis Sci 2011 Aug 22;52(9):6617-23       6 Citations
1Genetic variants of 6q25 and breast cancer susceptibility: a two-stage fine mapping study in a Chinese population. (Han J, Jiang T, Bai H, Gu H, Dong J, Ma H, Hu Z, Shen H) Breast Cancer Res Treat 2011 Oct;129(3):901-7       16 Citations
1Partial loss of Tip60 slows mid-stage neurodegeneration in a spinocerebellar ataxia type 1 (SCA1) mouse model. (Gehrking KM, Andresen JM, Duvick L, Lough J, Zoghbi HY, Orr HT) Hum Mol Genet 2011 Jun 01;20(11):2204-12       39 Citations
1Refined mapping of the renal failure RF-3 quantitative trait locus. (O'Meara CC, Lazar J, Hoffman M, Moreno C, Jacob HJ) J Am Soc Nephrol 2011 Mar;22(3):518-25       8 Citations
1Units of plasticity in bacterial genomes: new insight from the comparative genomics of two bacteria interacting with invertebrates, Photorhabdus and Xenorhabdus. (Ogier JC, Calteau A, Forst S, Goodrich-Blair H, Roche D, Rouy Z, Suen G, Zumbihl R, Givaudan A, Tailliez P, Médigue C, Gaudriault S) BMC Genomics 2010 Oct 15;11:568       30 Citations
1Identification of novel carcinogen-mediated mammary tumor susceptibility loci in the rat using the chromosome substitution technique. (Adamovic T, McAllister D, Wang T, Adamovic D, Rowe JJ, Moreno C, Lazar J, Jacob HJ, Sugg SL) Genes Chromosomes Cancer 2010 Nov;49(11):1035-45       10 Citations
1Analyzing complex traits with congenic strains. (Shao H, Sinasac DS, Burrage LC, Hodges CA, Supelak PJ, Palmert MR, Moreno C, Cowley AW Jr, Jacob HJ, Nadeau JH) Mamm Genome 2010 Jun;21(5-6):276-86       34 Citations
1Identifying physiological origins of baroreflex dysfunction in salt-sensitive hypertension in the Dahl SS rat. (Bugenhagen SM, Cowley AW Jr, Beard DA) Physiol Genomics 2010 Jun;42(1):23-41       35 Citations
1Deletion of ETS-1, a gene in the Jacobsen syndrome critical region, causes ventricular septal defects and abnormal ventricular morphology in mice. (Ye M, Coldren C, Liang X, Mattina T, Goldmuntz E, Benson DW, Ivy D, Perryman MB, Garrett-Sinha LA, Grossfeld P) Hum Mol Genet 2010 Feb 15;19(4):648-56       71 Citations
1Introgression of Brown Norway chromosome 1 onto the fawn hooded hypertensive background rescues long-term fear memory deficits. (Jarome TJ, Kwapis JL, Nye SH, Helmstetter FJ) Behav Genet 2010 Jan;40(1):85-92       5 Citations
1Implication of chromosome 13 on hypertension and associated disorders in Lyon hypertensive rats. (Gilibert S, Bataillard A, Nussberger J, Sassard J, Kwitek AE) J Hypertens 2009 Jun;27(6):1186-93       12 Citations
1Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. (Barrett JC, Clayton DG, Concannon P, Akolkar B, Cooper JD, Erlich HA, Julier C, Morahan G, Nerup J, Nierras C, Plagnol V, Pociot F, Schuilenburg H, Smyth DJ, Stevens H, Todd JA, Walker NM, Rich SS, Type 1 Diabetes Genetics Consortium) Nat Genet 2009 Jun;41(6):703-7       1109 Citations
1Sequence variation and expression of the Gimap gene family in the BB rat. (Rutledge EA, Fuller JM, Van Yserloo B, Moralejo DH, Ettinger RA, Gaur P, Hoehna JL, Peterson MR, Jensen R, Kwitek AE, Lernmark A) Exp Diabetes Res 2009;2009:835650       8 Citations
2Fine mapping of chromosome 6q23-25 region in familial lung cancer families reveals RGS17 as a likely candidate gene. (You M, Wang D, Liu P, Vikis H, James M, Lu Y, Wang Y, Wang M, Chen Q, Jia D, Liu Y, Wen W, Yang P, Sun Z, Pinney SM, Zheng W, Shu XO, Long J, Gao YT, Xiang YB, Chow WH, Rothman N, Petersen GM, de Andrade M, Wu Y, Cunningham JM, Wiest JS, Fain PR, Schwartz AG, Girard L, Gazdar A, Gaba C, Rothschild H, Mandal D, Coons T, Lee J, Kupert E, Seminara D, Minna J, Bailey-Wilson JE, Amos CI, Anderson MW) Clin Cancer Res 2009 Apr 15;15(8):2666-74       59 Citations
1Hypoplastic left heart syndrome links to chromosomes 10q and 6q and is genetically related to bicuspid aortic valve. (Hinton RB, Martin LJ, Rame-Gowda S, Tabangin ME, Cripe LH, Benson DW) J Am Coll Cardiol 2009 Mar 24;53(12):1065-71       99 Citations
1Congenic strains provide evidence that four mapped loci in chromosomes 2, 4, and 16 influence hypertension in the SHR. (Aneas I, Rodrigues MV, Pauletti BA, Silva GJ, Carmona R, Cardoso L, Kwitek AE, Jacob HJ, Soler JM, Krieger JE) Physiol Genomics 2009 Mar 03;37(1):52-7       15 Citations
1Genetic mapping of mammary tumor traits to rat chromosome 10 using a novel panel of consomic rats. (Adamovic T, McAllister D, Rowe JJ, Wang T, Jacob HJ, Sugg SL) Cancer Genet Cytogenet 2008 Oct;186(1):41-8       6 Citations
1Idd9/11 genetic locus regulates diabetogenic activity of CD4 T-cells in nonobese diabetic (NOD) mice. (Chen YG, Scheuplein F, Osborne MA, Tsaih SW, Chapman HD, Serreze DV) Diabetes 2008 Dec;57(12):3273-80       17 Citations
3Chromosome substitution reveals the genetic basis of Dahl salt-sensitive hypertension and renal disease. (Mattson DL, Dwinell MR, Greene AS, Kwitek AE, Roman RJ, Jacob HJ, Cowley AW Jr) Am J Physiol Renal Physiol 2008 Sep;295(3):F837-42       74 Citations
1Refining genetic associations in multiple sclerosis. (International Multiple Sclerosis Genetics Consortium (IMSGC)) Lancet Neurol 2008 Jul;7(7):567-9       80 Citations
1Quantitative trait loci mapping. (Xiong DH, Liu JF, Guo YF, Guo Y, Yang TL, Jiang H, Chen Y, Yang F, Recker RR, Deng HW) Methods Mol Biol 2008;455:203-35       2 Citations
2Progress and prospects in rat genetics: a community view. (Aitman TJ, Critser JK, Cuppen E, Dominiczak A, Fernandez-Suarez XM, Flint J, Gauguier D, Geurts AM, Gould M, Harris PC, Holmdahl R, Hubner N, Izsvák Z, Jacob HJ, Kuramoto T, Kwitek AE, Marrone A, Mashimo T, Moreno C, Mullins J, Mullins L, Olsson T, Pravenec M, Riley L, Saar K, Serikawa T, Shull JD, Szpirer C, Twigger SN, Voigt B, Worley K) Nat Genet 2008 May;40(5):516-22       206 Citations
1Ancestral bias in the Hras1 gene and distal Chromosome 7 among inbred mice. (Drew JC, Kastenmeier AS, Drinkwater NR) Mamm Genome 2007 Oct;18(10):732-8    
3Chromosomal mapping of the genetic basis of hypertension and renal disease in FHH rats. (Mattson DL, Dwinell MR, Greene AS, Kwitek AE, Roman RJ, Cowley AW Jr, Jacob HJ) Am J Physiol Renal Physiol 2007 Dec;293(6):F1905-14       39 Citations
1Identification and characterization of a major QTL responsible for erect panicle trait in japonica rice (Oryza sativa L.). (Yan CJ, Zhou JH, Yan S, Chen F, Yeboah M, Tang SZ, Liang GH, Gu MH) Theor Appl Genet 2007 Nov;115(8):1093-100       50 Citations
2Large-scale in silico mapping of complex quantitative traits in inbred mice. (Liu P, Vikis H, Lu Y, Wang D, You M) PLoS One 2007 Jul 25;2(7):e651       31 Citations
1Expression of SMARCB1 modulates steroid sensitivity in human lymphoblastoid cells: identification of a promoter SNP that alters PARP1 binding and SMARCB1 expression. (Pottier N, Cheok MH, Yang W, Assem M, Tracey L, Obenauer JC, Panetta JC, Relling MV, Evans WE) Hum Mol Genet 2007 Oct 01;16(19):2261-71       37 Citations
1A major genetic locus controlling natural Plasmodium falciparum infection is shared by East and West African Anopheles gambiae. (Riehle MM, Markianos K, Lambrechts L, Xia A, Sharakhov I, Koella JC, Vernick KD) Malar J 2007 Jul 06;6:87       20 Citations
2Multiple blood pressure loci on rat chromosome 13 attenuate development of hypertension in the Dahl S hypertensive rat. (Moreno C, Kaldunski ML, Wang T, Roman RJ, Greene AS, Lazar J, Jacob HJ, Cowley AW Jr) Physiol Genomics 2007 Oct 22;31(2):228-35       58 Citations
1Fine mapping and candidate gene analyses of pulmonary adenoma resistance 1, a major genetic determinant of mouse lung adenoma resistance. (Wang M, Zhang Z, Zhang Z, Vikis H, Yan Y, Wang Y, You M) Cancer Res 2007 Mar 15;67(6):2508-16       5 Citations
1Characterization of HKE2: an ancient antigen encoded in the major histocompatibility complex. (Ostrov DA, Barnes CL, Smith LE, Binns S, Brusko TM, Brown AC, Quint PS, Litherland SA, Roopenian DC, Iczkowski KA) Tissue Antigens 2007 Feb;69(2):181-8       7 Citations
1The Rat Genome Database, update 2007--easing the path from disease to data and back again. (Twigger SN, Shimoyama M, Bromberg S, Kwitek AE, Jacob HJ, RGD Team) Nucleic Acids Res 2007 Jan;35(Database issue):D658-62       104 Citations
1Introgression of F344 rat genomic DNA on BB rat chromosome 4 generates diabetes-resistant lymphopenic BB rats. (Fuller JM, Kwitek AE, Hawkins TJ, Moralejo DH, Lu W, Tupling TD, Macmurray AJ, Borchardt G, Hasinoff M, Lernmark A) Diabetes 2006 Dec;55(12):3351-7       15 Citations
1The genetic dissection of essential hypertension. (Cowley AW Jr) Nat Rev Genet 2006 Nov;7(11):829-40       216 Citations
1Genomic regions identified for BMD in a large sample including epistatic interactions and gender-specific effects. (Xiao P, Shen H, Guo YF, Xiong DH, Liu YZ, Liu YJ, Zhao LJ, Long JR, Guo Y, Recker RR, Deng HW) J Bone Miner Res 2006 Oct;21(10):1536-44       51 Citations
1Is a gene important for bone resorption a candidate for obesity? An association and linkage study on the RANK (receptor activator of nuclear factor-kappaB) gene in a large Caucasian sample. (Zhao LJ, Guo YF, Xiong DH, Xiao P, Recker RR, Deng HW) Hum Genet 2006 Nov;120(4):561-70       15 Citations
2Candidate lung tumor susceptibility genes identified through whole-genome association analyses in inbred mice. (Liu P, Wang Y, Vikis H, Maciag A, Wang D, Lu Y, Liu Y, You M) Nat Genet 2006 Aug;38(8):888-95       65 Citations
1Assessment of genetic linkage and parent-of-origin effects on obesity. (Guo YF, Shen H, Liu YJ, Wang W, Xiong DH, Xiao P, Liu YZ, Zhao LJ, Recker RR, Deng HW) J Clin Endocrinol Metab 2006 Oct;91(10):4001-5       28 Citations
1A genomewide scan for quantitative trait loci underlying areal bone size variation in 451 Caucasian families. (Shen H, Long JR, Xiong DH, Guo YF, Xiao P, Liu YZ, Zhao LJ, Liu YJ, Deng HY, Li JL, Recker RR, Deng HW) J Med Genet 2006 Nov;43(11):873-80       9 Citations
4Consomic strategies to localize genomic regions related to vascular reactivity in the Dahl salt-sensitive rat. (Kunert MP, Drenjancevic-Peric I, Dwinell MR, Lombard JH, Cowley AW Jr, Greene AS, Kwitek AE, Jacob HJ) Physiol Genomics 2006 Aug 16;26(3):218-25       23 Citations
1A population-based latent variable approach for association mapping of quantitative trait loci. (Wang T, Weir B, Zeng ZB) Ann Hum Genet 2006 Jul;70(Pt 4):506-23       3 Citations
1Natural malaria infection in Anopheles gambiae is regulated by a single genomic control region. (Riehle MM, Markianos K, Niaré O, Xu J, Li J, Touré AM, Podiougou B, Oduol F, Diawara S, Diallo M, Coulibaly B, Ouatara A, Kruglyak L, Traoré SF, Vernick KD) Science 2006 Apr 28;312(5773):577-9       206 Citations
1Impacts of QTL x environment interactions on genetic response to marker-assisted selection. (Liu PY, Zhu J, Yan L) Yi Chuan Xue Bao 2006 Jan;33(1):63-71       7 Citations
1Genetic linkage of human height is confirmed to 9q22 and Xq24. (Liu YZ, Xiao P, Guo YF, Xiong DH, Zhao LJ, Shen H, Liu YJ, Dvornyk V, Long JR, Deng HY, Li JL, Recker RR, Deng HW) Hum Genet 2006 Apr;119(3):295-304       25 Citations
1Genomewide linkage scan for quantitative trait loci underlying variation in age at menarche. (Guo Y, Shen H, Xiao P, Xiong DH, Yang TL, Guo YF, Long JR, Recker RR, Deng HW) J Clin Endocrinol Metab 2006 Mar;91(3):1009-14       45 Citations
1Impact of genomics on research in the rat. (Lazar J, Moreno C, Jacob HJ, Kwitek AE) Genome Res 2005 Dec;15(12):1717-28       50 Citations
1Genome-wide scan for linkage to obesity-associated hypertension in French Canadians. (Pausova Z, Gaudet D, Gossard F, Bernard M, Kaldunski ML, Jomphe M, Tremblay J, Hudson TJ, Bouchard G, Kotchen TA, Cowley AW, Hamet P) Hypertension 2005 Dec;46(6):1280-5       42 Citations
1Improvement of mapping accuracy by unifying linkage and association analysis. (Lou XY, Ma JZ, Yang MC, Zhu J, Liu PY, Deng HW, Elston RC, Li MD) Genetics 2006 Jan;172(1):647-61       5 Citations
1Searching for obesity genes: progress and prospects. (Liu YJ, Xiao P, Xiong DH, Recker RR, Deng HW) Drugs Today (Barc) 2005 May;41(5):345-62       8 Citations
1Fine mapping and evaluation of candidate genes for cervical cancer on 11q23. (Zhang Z, Gerhard DS, Nguyen L, Li J, Traugott A, Huettner PC, Rader JS) Genes Chromosomes Cancer 2005 May;43(1):95-103       14 Citations
3Genetic determinants on rat chromosome 6 modulate variation in the hypercapnic ventilatory response using consomic strains. (Dwinell MR, Forster HV, Petersen J, Rider A, Kunert MP, Cowley AW Jr, Jacob HJ) J Appl Physiol (1985) 2005 May;98(5):1630-8       13 Citations
1Substitution of chromosome 1 ameliorates L-NAME hypertension and renal disease in the fawn-hooded hypertensive rat. (Mattson DL, Kunert MP, Roman RJ, Jacob HJ, Cowley AW Jr) Am J Physiol Renal Physiol 2005 May;288(5):F1015-22       27 Citations
1Genetic linkage and association of the growth hormone secretagogue receptor (ghrelin receptor) gene in human obesity. (Baessler A, Hasinoff MJ, Fischer M, Reinhard W, Sonnenberg GE, Olivier M, Erdmann J, Schunkert H, Doering A, Jacob HJ, Comuzzie AG, Kissebah AH, Kwitek AE) Diabetes 2005 Jan;54(1):259-67       79 Citations
1The Rat Genome Database (RGD): developments towards a phenome database. (de la Cruz N, Bromberg S, Pasko D, Shimoyama M, Twigger S, Chen J, Chen CF, Fan C, Foote C, Gopinath GR, Harris G, Hughes A, Ji Y, Jin W, Li D, Mathis J, Nenasheva N, Nie J, Nigam R, Petri V, Reilly D, Wang W, Wu W, Zuniga-Meyer A, Zhao L, Kwitek A, Tonellato P, Jacob H) Nucleic Acids Res 2005 Jan 01;33(Database issue):D485-91       45 Citations
1Dimeric novel HSP40 is incorporated into the radial spoke complex during the assembly process in flagella. (Yang C, Compton MM, Yang P) Mol Biol Cell 2005 Feb;16(2):637-48       39 Citations
1Genetic dissection of human stature in a large sample of multiplex pedigrees. (Liu YZ, Xu FH, Shen H, Liu YJ, Zhao LJ, Long JR, Zhang YY, Xiao P, Xiong DH, Dvornyk V, Li JL, Conway T, Davies KM, Recker RR, Deng HW) Ann Hum Genet 2004 Sep;68(Pt 5):472-88       30 Citations
2Mapping the genetic determinants of hypertension, metabolic diseases, and related phenotypes in the lyon hypertensive rat. (Bilusic M, Bataillard A, Tschannen MR, Gao L, Barreto NE, Vincent M, Wang T, Jacob HJ, Sassard J, Kwitek AE) Hypertension 2004 Nov;44(5):695-701       46 Citations
1Consomic rat model systems for physiological genomics. (Cowley AW Jr, Liang M, Roman RJ, Greene AS, Jacob HJ) Acta Physiol Scand 2004 Aug;181(4):585-92       100 Citations
1A major lung cancer susceptibility locus maps to chromosome 6q23-25. (Bailey-Wilson JE, Amos CI, Pinney SM, Petersen GM, de Andrade M, Wiest JS, Fain P, Schwartz AG, You M, Franklin W, Klein C, Gazdar A, Rothschild H, Mandal D, Coons T, Slusser J, Lee J, Gaba C, Kupert E, Perez A, Zhou X, Zeng D, Liu Q, Zhang Q, Seminara D, Minna J, Anderson MW) Am J Hum Genet 2004 Sep;75(3):460-74    
1Detailed four-way comparative mapping and gene order analysis of the canine ctvm locus reveals evolutionary chromosome rearrangements. (Andelfinger G, Hitte C, Etter L, Guyon R, Bourque G, Tesler G, Pevzner P, Kirkness E, Galibert F, Benson DW) Genomics 2004 Jun;83(6):1053-62       19 Citations
1Integrative genomics: in silico coupling of rat physiology and complex traits with mouse and human data. (Twigger SN, Nie J, Ruotti V, Yu J, Chen D, Li D, Mathis J, Narayanasamy V, Gopinath GR, Pasko D, Shimoyama M, De La Cruz N, Bromberg S, Kwitek AE, Jacob HJ, Tonellato PJ) Genome Res 2004 Apr;14(4):651-60       17 Citations
1High-density rat radiation hybrid maps containing over 24,000 SSLPs, genes, and ESTs provide a direct link to the rat genome sequence. (Kwitek AE, Gullings-Handley J, Yu J, Carlos DC, Orlebeke K, Nie J, Eckert J, Lemke A, Andrae JW, Bromberg S, Pasko D, Chen D, Scheetz TE, Casavant TL, Soares MB, Sheffield VC, Tonellato PJ, Jacob HJ) Genome Res 2004 Apr;14(4):750-7       31 Citations
1Robust indices of Hardy-Weinberg disequilibrium for QTL fine mapping. (Deng HW, Li YM, Li MX, Liu PY) Hum Hered 2003;56(4):160-5       4 Citations
1Flagellar radial spoke protein 2 is a calmodulin binding protein required for motility in Chlamydomonas reinhardtii. (Yang P, Yang C, Sale WS) Eukaryot Cell 2004 Feb;3(1):72-81       43 Citations
1Genetic determinants of obesity-related lipid traits. (Sonnenberg GE, Krakower GR, Martin LJ, Olivier M, Kwitek AE, Comuzzie AG, Blangero J, Kissebah AH) J Lipid Res 2004 Apr;45(4):610-5       32 Citations
1Carcinogen-specific targeting of chromosome 12 for loss of heterozygosity in mouse lung adenocarcinomas: implications for chromosome instability and tumor progression. (Herzog CR, Bodon N, Pittman B, Maronpot RR, Massey TE, Anderson MW, You M, Devereux TR) Oncogene 2004 Apr 15;23(17):3033-9       17 Citations
1Differential expression of the closely linked KISS1, REN, and FLJ10761 genes in transgenic mice. (Nistala R, Zhang X, Sigmund CD) Physiol Genomics 2004 Mar 12;17(1):4-10       9 Citations
1Identifying genes and genetic variation underlying human diseases and complex phenotypes via recombination mapping. (Broeckel U, Schork NJ) J Physiol 2004 Jan 01;554(Pt 1):40-5       18 Citations
1Application of chromosomal substitution techniques in gene-function discovery. (Cowley AW Jr, Roman RJ, Jacob HJ) J Physiol 2004 Jan 01;554(Pt 1):46-55       90 Citations
1Positional cloning of the major quantitative trait locus underlying lung tumor susceptibility in mice. (Zhang Z, Futamura M, Vikis HG, Wang M, Li J, Wang Y, Guan KL, You M) Proc Natl Acad Sci U S A 2003 Oct 28;100(22):12642-7       35 Citations
1A candidate locus approach identifies a long QT syndrome gene mutation. (Beery TA, Dyment M, Shooner K, Knilans TK, Benson DW) Biol Res Nurs 2003 Oct;5(2):97-104       4 Citations
1Genomic map of cardiovascular phenotypes of hypertension in female Dahl S rats. (Moreno C, Dumas P, Kaldunski ML, Tonellato PJ, Greene AS, Roman RJ, Cheng Q, Wang Z, Jacob HJ, Cowley AW Jr) Physiol Genomics 2003 Nov 11;15(3):243-57       82 Citations
1Paradoxical decrease in mutant frequencies and chromosomal rearrangements in a transgenic lacZ reporter gene in Ku80 null mice deficient in DNA double strand break repair. (Rockwood LD, Nussenzweig A, Janz S) Mutat Res 2003 Aug 28;529(1-2):51-8       14 Citations
1Serial analysis of gene expression. (el-Meanawy MA, Barathan S, Hayden PS, Iyengar SK, Schelling JR, Sedor JR) Methods Mol Med 2003;86:257-74       3 Citations
1Characterization of FRA6E and its potential role in autosomal recessive juvenile parkinsonism and ovarian cancer. (Denison SR, Callahan G, Becker NA, Phillips LA, Smith DI) Genes Chromosomes Cancer 2003 Sep;38(1):40-52       104 Citations
1A single nucleotide polymorphism in the Emp3 gene defines the H4 minor histocompatibility antigen. (Luedtke B, Pooler LM, Choi EY, Tranchita AM, Reinbold CJ, Brown AC, Shaffer DJ, Roopenian DC, Malarkannan S) Immunogenetics 2003 Aug;55(5):284-95       11 Citations
1The rat STSL locus: characterization, chromosomal assignment, and genetic variations in sitosterolemic hypertensive rats. (Yu H, Pandit B, Klett E, Lee MH, Lu K, Helou K, Ikeda I, Egashira N, Sato M, Klein R, Batta A, Salen G, Patel SB) BMC Cardiovasc Disord 2003 Jun 03;3:4       30 Citations
1Canine tricuspid valve malformation, a model of human Ebstein anomaly, maps to dog chromosome 9. (Andelfinger G, Wright KN, Lee HS, Siemens LM, Benson DW) J Med Genet 2003 May;40(5):320-4       63 Citations
1E mu/S mu transposition into Myc is sometimes a precursor for T(12;15) translocation in mouse B cells. (Kovalchuk AL, Kim JS, Janz S) Oncogene 2003 May 08;22(18):2842-50       7 Citations
1Genomics and homeostasis. (Cowley AW Jr) Am J Physiol Regul Integr Comp Physiol 2003 Mar;284(3):R611-27       46 Citations
3Identification of hypertension-related QTLs in African American sib pairs. (Kotchen TA, Broeckel U, Grim CE, Hamet P, Jacob H, Kaldunski ML, Kotchen JM, Schork NJ, Tonellato PJ, Cowley AW Jr) Hypertension 2002 Nov;40(5):634-9       22 Citations
1Isotype switch-mediated CH deletions are a recurrent feature of Myc/CH translocations in peritoneal plasmacytomas in mice. (Kovalchuk AL, Janz S) Int J Cancer 2002 Oct 10;101(5):423-6       5 Citations
1Refinement of the autosomal recessive polycystic kidney disease (PKHD1) interval and exclusion of an EF hand-containing gene as a PKHD1 candidate gene. (Onuchic LF, Mrug M, Hou X, Eggermann T, Bergmann C, Zerres K, Avner ED, Furu L, Somlo S, Nagasawa Y, Germino GG, Guay-Woodford LM) Am J Med Genet 2002 Jul 15;110(4):346-52       17 Citations
1Mapping baroreceptor function to genome: a mathematical modeling approach. (Kendziorski CM, Cowley AW Jr, Greene AS, Salgado HC, Jacob HJ, Tonellato PJ) Genetics 2002 Apr;160(4):1687-95       10 Citations
1A comprehensive linkage analysis for myocardial infarction and its related risk factors. (Broeckel U, Hengstenberg C, Mayer B, Holmer S, Martin LJ, Comuzzie AG, Blangero J, Nürnberg P, Reis A, Riegger GA, Jacob HJ, Schunkert H) Nat Genet 2002 Feb;30(2):210-4       273 Citations
1IL-6 transgenic mouse model for extraosseous plasmacytoma. (Kovalchuk AL, Kim JS, Park SS, Coleman AE, Ward JM, Morse HC 3rd, Kishimoto T, Potter M, Janz S) Proc Natl Acad Sci U S A 2002 Feb 05;99(3):1509-14       104 Citations
1Rat Genome Database (RGD): mapping disease onto the genome. (Twigger S, Lu J, Shimoyama M, Chen D, Pasko D, Long H, Ginster J, Chen CF, Nigam R, Kwitek A, Eppig J, Maltais L, Maglott D, Schuler G, Jacob H, Tonellato PJ) Nucleic Acids Res 2002 Jan 01;30(1):125-8       78 Citations
1A genomic-systems biology map for cardiovascular function. (Stoll M, Cowley AW Jr, Tonellato PJ, Greene AS, Kaldunski ML, Roman RJ, Dumas P, Schork NJ, Wang Z, Jacob HJ) Science 2001 Nov 23;294(5547):1723-6       149 Citations
1Automated construction of high-density comparative maps between rat, human, and mouse. (Kwitek AE, Tonellato PJ, Chen D, Gullings-Handley J, Cheng YS, Twigger S, Scheetz TE, Casavant TL, Stoll M, Nobrega MA, Shiozawa M, Soares MB, Sheffield VC, Jacob HJ) Genome Res 2001 Nov;11(11):1935-43       33 Citations
1Wildtype Kras2 can inhibit lung carcinogenesis in mice. (Zhang Z, Wang Y, Vikis HG, Johnson L, Liu G, Li J, Anderson MW, Sills RC, Hong HL, Devereux TR, Jacks T, Guan KL, You M) Nat Genet 2001 Sep;29(1):25-33       233 Citations
1Large cell/anaplastic medulloblastomas and medullomyoblastomas: clinicopathological and genetic features. (Leonard JR, Cai DX, Rivet DJ, Kaufman BA, Park TS, Levy BK, Perry A) J Neurosurg 2001 Jul;95(1):82-8       89 Citations
1Conformational differences in the 3-D nanostructure of the immunoglobulin heavy-chain locus, a hotspot of chromosomal translocations in B lymphocytes. (Esa A, Coleman AE, Edelmann P, Silva S, Cremer CG, Janz S) Cancer Genet Cytogenet 2001 Jun;127(2):168-73       21 Citations
1Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2). (Nishimura DY, Searby CC, Carmi R, Elbedour K, Van Maldergem L, Fulton AB, Lam BL, Powell BR, Swiderski RE, Bugge KE, Haider NB, Kwitek-Black AE, Ying L, Duhl DM, Gorman SW, Heon E, Iannaccone A, Bonneau D, Biesecker LG, Jacobson SG, Stone EM, Sheffield VC) Hum Mol Genet 2001 Apr 01;10(8):865-74       192 Citations
1Translocation remodeling in the primary BALB/c plasmacytoma TEPC 3610. (Kovalchuk AL, Esa A, Coleman AE, Park SS, Ried T, Cremer CC, Janz S) Genes Chromosomes Cancer 2001 Mar;30(3):283-91       10 Citations
1Retinoic acid-induced tissue transglutaminase and apoptosis in vascular smooth muscle cells. (Ou H, Haendeler J, Aebly MR, Kelly LA, Cholewa BC, Koike G, Kwitek-Black A, Jacob HJ, Berk BC, Miano JM) Circ Res 2000 Nov 10;87(10):881-7       52 Citations
1High-throughput scanning of the rat genome using interspersed repetitive sequence-PCR markers. (Gösele C, Hong L, Kreitler T, Rossmann M, Hieke B, Gross U, Kramer M, Himmelbauer H, Bihoreau MT, Kwitek-Black AE, Twigger S, Tonellato PJ, Jacob HJ, Schalkwyk LC, Lindpaintner K, Ganten D, Lehrach H, Knoblauch M) Genomics 2000 Nov 01;69(3):287-94       12 Citations
1Role of tumor necrosis factor-alpha gene locus in obesity and obesity-associated hypertension in French Canadians. (Pausova Z, Deslauriers B, Gaudet D, Tremblay J, Kotchen TA, Larochelle P, Cowley AW, Hamet P) Hypertension 2000 Jul;36(1):14-9       87 Citations
1Clonal diversification of primary BALB/c plasmacytomas harboring T(12;15) chromosomal translocations. (Kovalchuk AL, Mushinski EB, Janz S) Leukemia 2000 May;14(5):909-21       17 Citations
1Genomic structure of the gene for the human P1 protein (MCM3) and its exclusion as a candidate for autosomal recessive polycystic kidney disease. (Hofmann Y, Becker J, Wright F, Avner ED, Mrug M, Guay-Woodford LM, Somlo S, Zerres K, Germino GG, Onuchic LF) Eur J Hum Genet 2000 Mar;8(3):163-6       7 Citations
1Isolation and characterization of a novel human paired-like homeodomain-containing transcription factor gene, VSX1, expressed in ocular tissues. (Semina EV, Mintz-Hittner HA, Murray JC) Genomics 2000 Jan 15;63(2):289-93       72 Citations
1Appropriate tissue- and cell-specific expression of a single copy human angiotensinogen transgene specifically targeted upstream of the HPRT locus by homologous recombination. (Cvetkovic B, Yang B, Williamson RA, Sigmund CD) J Biol Chem 2000 Jan 14;275(2):1073-8       41 Citations
1Molecular cloning, tissue-specific expression, and chromosomal localization of a novel nerve growth factor-regulated G-protein- coupled receptor, nrg-1. (Glickman M, Malek RL, Kwitek-Black AE, Jacob HJ, Lee NH) Mol Cell Neurosci 1999 Aug;14(2):141-52       67 Citations
1Detailed genetic and physical mapping of tumor suppressor loci on chromosome 3p in ovarian cancer. (Fullwood P, Marchini S, Rader JS, Martinez A, Macartney D, Broggini M, Morelli C, Barbanti-Brodano G, Maher ER, Latif F) Cancer Res 1999 Sep 15;59(18):4662-7       55 Citations
1A high-density integrated genetic linkage and radiation hybrid map of the laboratory rat. (Steen RG, Kwitek-Black AE, Glenn C, Gullings-Handley J, Van Etten W, Atkinson OS, Appel D, Twigger S, Muir M, Mull T, Granados M, Kissebah M, Russo K, Crane R, Popp M, Peden M, Matise T, Brown DM, Lu J, Kingsmore S, Tonellato PJ, Rozen S, Slonim D, Young P, Jacob HJ) Genome Res 1999 Jun;9(6):AP1-8, insert       177 Citations
1The critical interaction of glycoprotein (GP) IBbeta with GPIX-a genetic cause of Bernard-Soulier syndrome. (Kenny D, Morateck PA, Gill JC, Montgomery RR) Blood 1999 May 01;93(9):2968-75       61 Citations
1Familial dilated cardiomyopathy locus maps to chromosome 2q31. (Siu BL, Niimura H, Osborne JA, Fatkin D, MacRae C, Solomon S, Benson DW, Seidman JG, Seidman CE) Circulation 1999 Mar 02;99(8):1022-6       110 Citations
1Frequent deletions within FRA7G at 7q31.2 in invasive epithelial ovarian cancer. (Huang H, Reed CP, Mordi A, Lomberk G, Wang L, Shridhar V, Hartmann L, Jenkins R, Smith DI) Genes Chromosomes Cancer 1999 Jan;24(1):48-55       40 Citations
1Cloning and chromosomal localization of two novel human genes encoding LIM-domain binding factors CLIM1 and CLIM2/LDB1/NLI. (Semina EV, Altherr MR, Murray JC) Mamm Genome 1998 Nov;9(11):921-4       10 Citations
1Assignment of gene responsible for progressive pseudorheumatoid dysplasia to chromosome 6 and examination of COL10A1 as candidate gene. (el-Shanti H, Murray JC, Semina EV, Beutow KH, Scherpbier T, al-Alami J) Eur J Hum Genet 1998 May-Jun;6(3):251-6       17 Citations
1Mapping an endometrial cancer tumor suppressor gene at 10q25 and development of a bacterial clone contig for the consensus deletion interval. (Peiffer-Schneider S, Noonan FC, Mutch DG, Simpkins SB, Herzog T, Rader J, Elbendary A, Gersell DJ, Call K, Goodfellow PJ) Genomics 1998 Aug 15;52(1):9-16       27 Citations
1Congenital heart disease caused by mutations in the transcription factor NKX2-5. (Schott JJ, Benson DW, Basson CT, Pease W, Silberbach GM, Moak JP, Maron BJ, Seidman CE, Seidman JG) Science 1998 Jul 03;281(5373):108-11       986 Citations
1A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD. (Semina EV, Ferrell RE, Mintz-Hittner HA, Bitoun P, Alward WL, Reiter RS, Funkhauser C, Daack-Hirsch S, Murray JC) Nat Genet 1998 Jun;19(2):167-70       313 Citations
1Reduced penetrance, variable expressivity, and genetic heterogeneity of familial atrial septal defects. (Benson DW, Sharkey A, Fatkin D, Lang P, Basson CT, McDonough B, Strauss AW, Seidman JG, Seidman CE) Circulation 1998 May 26;97(20):2043-8       67 Citations
1Cloning and chromosomal mapping of the murine norepinephrine transporter. (Fritz JD, Jayanthi LD, Thoreson MA, Blakely RD) J Neurochem 1998 Jun;70(6):2241-51       45 Citations
1A new human homeobox gene OGI2X is a member of the most conserved homeobox gene family and is expressed during heart development in mouse. (Semina EV, Reiter RS, Murray JC) Hum Mol Genet 1998 Mar;7(3):415-22       46 Citations
1Identification of type III secreted products of the Pseudomonas aeruginosa exoenzyme S regulon. (Yahr TL, Mende-Mueller LM, Friese MB, Frank DW) J Bacteriol 1997 Nov;179(22):7165-8       171 Citations
1Isolation of a new homeobox gene belonging to the Pitx/Rieg family: expression during lens development and mapping to the aphakia region on mouse chromosome 19. (Semina EV, Reiter RS, Murray JC) Hum Mol Genet 1997 Nov;6(12):2109-16       157 Citations
1Previously hidden chromosome aberrations in T(12;15)-positive BALB/c plasmacytomas uncovered by multicolor spectral karyotyping. (Coleman AE, Schröck E, Weaver Z, du Manoir S, Yang F, Ferguson-Smith MA, Ried T, Janz S) Cancer Res 1997 Oct 15;57(20):4585-92       38 Citations
1ExoU expression by Pseudomonas aeruginosa correlates with acute cytotoxicity and epithelial injury. (Finck-Barbançon V, Goranson J, Zhu L, Sawa T, Wiener-Kronish JP, Fleiszig SM, Wu C, Mende-Mueller L, Frank DW) Mol Microbiol 1997 Aug;25(3):547-57       366 Citations
1An integrated genetic and physical map of the autosomal recessive polycystic kidney disease region. (Lens XM, Onuchic LF, Wu G, Hayashi T, Daoust M, Mochizuki T, Santarina LB, Stockwin JM, Mücher G, Becker J, Sweeny WE Jr, Avner ED, Guay-Woodford L, Zerres K, Somlo S, Germino GG) Genomics 1997 May 01;41(3):463-6       30 Citations
1Exclusion of epidermal growth factor and high-resolution physical mapping across the Rieger syndrome locus. (Semina EV, Datson NA, Leysens NJ, Zabel BU, Carey JC, Bell GI, Bitoun P, Lindgren C, Stevenson T, Frants RR, van Ommen G, Murray JC) Am J Hum Genet 1996 Dec;59(6):1288-96       21 Citations
1PCR-based gene targeting of the inducible nitric oxide synthase (NOS2) locus in murine ES cells, a new and more cost-effective approach. (Randolph DA, Verbsky JW, Yang L, Fang Y, Hakem R, Fields LE) Transgenic Res 1996 Nov;5(6):413-20       6 Citations
1Evidence that two phenotypically distinct mouse PKD mutations, bpk and jcpk, are allelic. (Guay-Woodford LM, Bryda EC, Christine B, Lindsey JR, Collier WR, Avner ED, D'Eustachio P, Flaherty L) Kidney Int 1996 Oct;50(4):1158-65       31 Citations
1Role of proximal promoter elements in regulation of renin gene transcription. (Petrovic N, Black TA, Fabian JR, Kane C, Jones CA, Loudon JA, Abonia JP, Sigmund CD, Gross KW) J Biol Chem 1996 Sep 13;271(37):22499-505       94 Citations
1Linkage of congenital isolated adrenocorticotropic hormone deficiency to the corticotropin releasing hormone locus using simple sequence repeat polymorphisms. (Kyllo JH, Collins MM, Vetter KL, Cuttler L, Rosenfield RL, Donohoue PA) Am J Med Genet 1996 Mar 29;62(3):262-7       22 Citations
1Functional and regulatory analysis of the OmpF-like porin, OpnP, of the symbiotic bacterium Xenorhabdus nematophilus. (Forst S, Waukau J, Leisman G, Exner M, Hancock R) Mol Microbiol 1995 Nov;18(4):779-89       21 Citations
1Persistence of immunoglobulin heavy chain/c-myc recombination-positive lymphocyte clones in the blood of human immunodeficiency virus-infected homosexual men. (Müller JR, Janz S, Goedert JJ, Potter M, Rabkin CS) Proc Natl Acad Sci U S A 1995 Jul 03;92(14):6577-81       64 Citations
1A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3. (White PS, Maris JM, Beltinger C, Sulman E, Marshall HN, Fujimori M, Kaufman BA, Biegel JA, Allen C, Hilliard C, Valentine MB, Look AT, Enomoto H, Sakiyama S, Brodeur GM) Proc Natl Acad Sci U S A 1995 Jun 06;92(12):5520-4       228 Citations
1The severe perinatal form of autosomal recessive polycystic kidney disease maps to chromosome 6p21.1-p12: implications for genetic counseling. (Guay-Woodford LM, Muecher G, Hopkins SD, Avner ED, Germino GG, Guillot AP, Herrin J, Holleman R, Irons DA, Primack W) Am J Hum Genet 1995 May;56(5):1101-7       142 Citations
1Localization of the murine homolog of the anaplastic lymphoma kinase (AlK) gene on mouse chromosome 17. (Mathew P, Morris SW, Kane JR, Shurtleff SA, Pasquini M, Jenkins NA, Gilbert DJ, Copeland NG) Cytogenet Cell Genet 1995;70(1-2):143-4       11 Citations
1Differences in the molecular structure of c-myc-activating recombinations in murine plasmacytomas and precursor cells. (Müller JR, Potter M, Janz S) Proc Natl Acad Sci U S A 1994 Dec 06;91(25):12066-70       34 Citations
1Integration of 28 STSs into the physical map of human chromosome 18. (Gerken S, Fish K, Uyar D, Polymeropoulos MH, Bradley P, White R, Overhauser J, Silverman GA) Genomics 1994 Dec;24(3):612-3       10 Citations
1Liddle's syndrome: heritable human hypertension caused by mutations in the beta subunit of the epithelial sodium channel. (Shimkets RA, Warnock DG, Bositis CM, Nelson-Williams C, Hansson JH, Schambelan M, Gill JR Jr, Ulick S, Milora RV, Findling JW) Cell 1994 Nov 04;79(3):407-14       1122 Citations
1Linkage mapping of the tumor necrosis factor receptor 2 (TNFR2) gene to 1p36.2 using the single-strand conformation polymorphism technique. (Kaufman BA, White PS, Steinbrueck T, Donis-Keller H, Brodeur GM) Hum Genet 1994 Oct;94(4):418-22       9 Citations
1Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mapping. (Sheffield VC, Carmi R, Kwitek-Black A, Rokhlina T, Nishimura D, Duyk GM, Elbedour K, Sunden SL, Stone EM) Hum Mol Genet 1994 Aug;3(8):1331-5       181 Citations
1Regional localization of 56 new human chromosome 18-specific yeast artificial chromosomes. (Chang E, Luna J, Giacalone J, Uyar D, Silverman GA, Francke U) Cytogenet Cell Genet 1994;65(1-2):136-9       3 Citations
1Characterization of the region of consistent deletion within 1p36 in neuroblastomas. (White PS, Fujimori M, Marshall HN, Kaufman BA, Brodeur GM) Prog Clin Biol Res 1994;385:3-9       4 Citations
1Linkage of Bardet-Biedl syndrome to chromosome 16q and evidence for non-allelic genetic heterogeneity. (Kwitek-Black AE, Carmi R, Duyk GM, Buetow KH, Elbedour K, Parvari R, Yandava CN, Stone EM, Sheffield VC) Nat Genet 1993 Dec;5(4):392-6       147 Citations
1Identification of a colon mucosa gene that is down-regulated in colon adenomas and adenocarcinomas. (Schweinfest CW, Henderson KW, Suster S, Kondoh N, Papas TS) Proc Natl Acad Sci U S A 1993 May 01;90(9):4166-70       178 Citations
1Clinical features and linkage analysis of a family with autosomal dominant juvenile glaucoma. (Johnson AT, Drack AV, Kwitek AE, Cannon RL, Stone EM, Alward WL) Ophthalmology 1993 Apr;100(4):524-9       91 Citations
1Alleles of the rat T-cell receptor beta chain gene complex. (Blankenhorn EP, Smith PD, Williams CB, Gutman GA) Immunogenetics 1992;35(5):324-31       10 Citations
1Mapping of human chromosome 5 microsatellite DNA polymorphisms. (Weber JL, Polymeropoulos MH, May PE, Kwitek AE, Xiao H, McPherson JD, Wasmuth JJ) Genomics 1991 Nov;11(3):695-700       77 Citations
1Structure, expression, and regulation of the murine renin genes. (Sigmund CD, Gross KW) Hypertension 1991 Oct;18(4):446-57       106 Citations
1Linkage mapping of D21S171 to the distal long arm of human chromosome 21 using a polymorphic (AC)n dinucleotide repeat. (Petersen MB, Weber JL, Slaugenhaupt SA, Kwitek AE, McInnis MG, Chakravarti A, Antonarakis SE) Hum Genet 1991 Aug;87(4):401-4       12 Citations
1Organization and nucleotide sequence of the rat T cell receptor beta-chain complex. (Williams CB, Blankenhorn EP, Byrd KE, Levinson G, Gutman GA) J Immunol 1991 Jun 15;146(12):4406-13       42 Citations
1An MspI polymorphism in the human acid sphingomyelinase gene (SMPD1). (Schuchman EH, Levran O, Suchi M, Desnick RJ) Nucleic Acids Res 1991 Jun 11;19(11):3160       11 Citations
1Dinucleotide repeat polymorphism at the D6S105 locus. (Weber JL, Kwitek AE, May PE, Zoghbi HY) Nucleic Acids Res 1991 Feb 25;19(4):968       58 Citations
1Linkage mapping of the highly informative DNA marker D21S156 to human chromosome 21 using a polymorphic GT dinucleotide repeat. (Lewis JG, Weber JL, Petersen MB, Slaugenhaupt SA, Kwitek A, May PE, Warren AC, Chakravarti A, Antonarakis SE) Genomics 1990 Oct;8(2):400-2       17 Citations
1Dinucleotide repeat polymorphisms at the D11S419 and CD3D loci. (Weber JL, Kwitek AE, May PE) Nucleic Acids Res 1990 Jul 11;18(13):4036       22 Citations
1Dinucleotide repeat polymorphisms at the D16S260, D16S261, D16S265, D16S266, and D16S267 loci. (Weber JL, Kwitek AE, May PE) Nucleic Acids Res 1990 Jul 11;18(13):4034       31 Citations
1Dinucleotide repeat polymorphisms at the D5S107, D5S108, D5S111, D5S117 and D5S118 loci. (Weber JL, Kwitek AE, May PE) Nucleic Acids Res 1990 Jul 11;18(13):4035       34 Citations
1Dinucleotide repeat polymorphisms at the D7S435 and D7S440 loci. (Weber JL, Kwitek AE, May PE) Nucleic Acids Res 1990 Jul 11;18(13):4039       34 Citations
1Dinucleotide repeat polymorphisms at the D8S85, D8S87, and D8S88 loci. (Weber JL, Kwitek AE, May PE, Patterson D, Drabkin H) Nucleic Acids Res 1990 Jul 11;18(13):4038       39 Citations
1Dinucleotide repeat polymorphisms at the DXS453, DXS454 and DXS458 loci. (Weber JL, Kwitek AE, May PE, Polymeropoulos MH, Ledbetter S) Nucleic Acids Res 1990 Jul 11;18(13):4037       45 Citations
1Dinucleotide repeat polymorphism at the D1S102 locus. (Weber JL, Kwitek AE, May PE) Nucleic Acids Res 1990 Apr 25;18(8):2199       19 Citations
1Dinucleotide repeat polymorphism at the D1S103 locus. (Weber JL, Kwitek AE, May PE) Nucleic Acids Res 1990 Apr 25;18(8):2199    
1Deoxyglucose-resistant mutants of Neurospora crassa: isolation, mapping, and biochemical characterization. (Allen KE, McNally MT, Lowendorf HS, Slayman CW, Free SJ) J Bacteriol 1989 Jan;171(1):53-8       45 Citations
1Coupling of HLA-A3,Cw6,Bw47,DR7 and a normal CA21HB steroid 21-hydroxylase gene in the Old Order Amish. (Donohoue PA, Van Dop C, Migeon CJ, McLean RH, Bias WB) J Clin Endocrinol Metab 1987 Nov;65(5):980-6       6 Citations
1Molecular structure of a somatically unstable transposable element in Drosophila. (Jacobson JW, Medhora MM, Hartl DL) Proc Natl Acad Sci U S A 1986 Nov;83(22):8684-8       230 Citations
1Gene conversion in salt-losing congenital adrenal hyperplasia with absent complement C4B protein. (Donohoue PA, van Dop C, McLean RH, White PC, Jospe N, Migeon CJ) J Clin Endocrinol Metab 1986 May;62(5):995-1002       96 Citations
1Integration of bacteriophage Mu at host chromosomal replication forks during lytic development. (Fitts RA, Taylor AL) Proc Natl Acad Sci U S A 1980 May;77(5):2801-5       7 Citations
1HLA antigens of platelets. IV. Influence of "private" HLA--B locus specificities on the expression of Bw4 and Bw6 on human platelets. (Szatkowski NS, Aster RH) Tissue Antigens 1980 Apr;15(4):361-8       17 Citations
1Further studies of the expression of Bw4, Bw6, and other antigens of the HLA-B locus on human platelets. (Szatkowski N, Duquesnoy RJ, Aster RH) Transplant Proc 1978 Dec;10(4):739-40       4 Citations
jenkins-FCD Prod-480 9a4deaf152b0b06dd18151814fff2e18f6c05280