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1 | Multisite Assessment of Optical Genome Mapping for Analysis of Structural Variants in Constitutional Postnatal Cases. (Iqbal MA, Broeckel U, Levy B, Skinner S, Sahajpal NS, Rodriguez V, Stence A, Awayda K, Scharer G, Skinner C, Stevenson R, Bossler A, Nagy PL, Kolhe R) J Mol Diagn 2023 Mar;25(3):175-188 30 Citations |
1 | Admixture Mapping in African Americans Identifies New Risk Loci for HCV-Related Cirrhosis. (Kim HS, Shetty PB, Tsavachidis S, Dong J, Amos CI, El-Serag HB, Thrift AP) Clin Gastroenterol Hepatol 2023 Apr;21(4):1023-1030.e39 |
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5 | The 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 Jan 08;48(D1):D731-D742 115 Citations |
1 | Rat Genome Assemblies, Annotation, and Variant Repository. (Tutaj M, Smith JR, Bolton ER) Methods Mol Biol 2019;2018:43-70 6 Citations |
1 | Mapping Mammary Tumor Traits in the Rat. (Flister MJ, Joshi A, Bergom C, Rui H) Methods Mol Biol 2019;2018:249-267 4 Citations |
3 | Identification 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 May 07;9(5):1739-1743 6 Citations |
1 | Combined congenic mapping and nuclease-based gene targeting for studying allele-specific effects of Tnfrsf9 within the Idd9.3 autoimmune diabetes locus. (Forsberg MH, Foda B, Serreze DV, Chen YG) Sci Rep 2019 Mar 13;9(1):4316 9 Citations |
2 | Mapping 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 Jun 01;316(6):H1267-H1280 36 Citations |
1 | Three-dimensional analysis reveals altered chromatin interaction by enhancer inhibitors harbors TCF7L2-regulated cancer gene signature. (Gerrard DL, Wang Y, Gaddis M, Zhou Y, Wang J, Witt H, Lin S, Farnham PJ, Jin VX, Frietze SE) J Cell Biochem 2019 Mar;120(3):3056-3070 9 Citations |
1 | A High-Resolution Genetic Map for the Laboratory Rat. (Littrell J, Tsaih SW, Baud A, Rastas P, Solberg-Woods L, Flister MJ) G3 (Bethesda) 2018 Jul 02;8(7):2241-2248 14 Citations |
1 | Genome-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 May 01;50(5):323-331 6 Citations |
1 | Genetic Fine-Mapping and Identification of Candidate Genes and Variants for Adiposity Traits in Outbred Rats. (Keele GR, Prokop JW, He H, Holl K, Littrell J, Deal A, Francic S, Cui L, Gatti DM, Broman KW, Tschannen M, Tsaih SW, Zagloul M, Kim Y, Baur B, Fox J, Robinson M, Levy S, Flister MJ, Mott R, Valdar W, Solberg Woods LC) Obesity (Silver Spring) 2018 Jan;26(1):213-222 52 Citations |
1 | Fine 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 Aug 01;141(3):447-456 17 Citations |
1 | Congenic 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 Mar;69(3):193-198 2 Citations |
1 | Copy-number variation is an important contributor to the genetic causality of inherited retinal degenerations. (Bujakowska KM, Fernandez-Godino R, Place E, Consugar M, Navarro-Gomez D, White J, Bedoukian EC, Zhu X, Xie HM, Gai X, Leroy BP, Pierce EA) Genet Med 2017 Jun;19(6):643-651 50 Citations |
1 | Genetic Architectures of Quantitative Variation in RNA Editing Pathways. (Gu T, Gatti DM, Srivastava A, Snyder EM, Raghupathy N, Simecek P, Svenson KL, Dotu I, Chuang JH, Keller MP, Attie AD, Braun RE, Churchill GA) Genetics 2016 Feb;202(2):787-98 18 Citations |
1 | Association 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 17 Citations |
1 | Fine 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):381-6 518 Citations |
2 | A 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;16(3):221-30 7 Citations |
1 | Comparative genomic analysis of nine Sphingobium strains: insights into their evolution and hexachlorocyclohexane (HCH) degradation pathways. (Verma H, Kumar R, Oldach P, Sangwan N, Khurana JP, Gilbert JA, Lal R) BMC Genomics 2014 Nov 23;15(1):1014 65 Citations |
1 | Genome 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 90 Citations |
1 | Pathogenic variants for Mendelian and complex traits in exomes of 6,517 European and African Americans: implications for the return of incidental results. (Tabor HK, Auer PL, Jamal SM, Chong JX, Yu JH, Gordon AS, Graubert TA, O'Donnell CJ, Rich SS, Nickerson DA, NHLBI Exome Sequencing Project, Bamshad MJ) Am J Hum Genet 2014 Aug 07;95(2):183-93 69 Citations |
1 | TNNI3K 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 47 Citations |
1 | Post-GWAS gene-environment interplay in breast cancer: results from the Breast and Prostate Cancer Cohort Consortium and a meta-analysis on 79,000 women. (Barrdahl M, Canzian F, Joshi AD, Travis RC, Chang-Claude J, Auer PL, Gapstur SM, Gaudet M, Diver WR, Henderson BE, Haiman CA, Schumacher FR, Le Marchand L, Berg CD, Chanock SJ, Hoover RN, Rudolph A, Ziegler RG, Giles GG, Baglietto L, Severi G, Hankinson SE, Lindström S, Willet W, Hunter DJ, Buring JE, Lee IM, Zhang S, Dossus L, Cox DG, Khaw KT, Lund E, Naccarati A, Peeters PH, Quirós JR, Riboli E, Sund M, Trichopoulos D, Prentice RL, Kraft P, Kaaks R, Campa D) Hum Mol Genet 2014 Oct 01;23(19):5260-70 35 Citations |
1 | Genomic 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(1):197 9 Citations |
1 | Loci 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):1663-78 111 Citations |
1 | Discovery 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 64 Citations |
1 | Genetic 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 30 Citations |
1 | Fine-mapping diabetes-related traits, including insulin resistance, in heterogeneous stock rats. (Solberg Woods LC, Holl KL, Oreper D, Xie Y, Tsaih SW, Valdar W) Physiol Genomics 2012 Nov 01;44(21):1013-26 37 Citations |
1 | Genotype 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 12 Citations |
1 | A 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 6 Citations |
1 | Genetic 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 39 Citations |
1 | Positional cloning of a type 2 diabetes quantitative trait locus; tomosyn-2, a negative regulator of insulin secretion. (Bhatnagar S, Oler AT, Rabaglia ME, Stapleton DS, Schueler KL, Truchan NA, Worzella SL, Stoehr JP, Clee SM, Yandell BS, Keller MP, Thurmond DC, Attie AD) PLoS Genet 2011 Oct;7(10):e1002323 60 Citations |
1 | On coding genotypes for genetic markers with multiple alleles in genetic association study of quantitative traits. (Wang T) BMC Genet 2011 Sep 21;12:82 8 Citations |
1 | ChIP-seq defined genome-wide map of TGFβ/SMAD4 targets: implications with clinical outcome of ovarian cancer. (Kennedy BA, Deatherage DE, Gu F, Tang B, Chan MW, Nephew KP, Huang TH, Jin VX) PLoS One 2011;6(7):e22606 30 Citations |
1 | Characterization 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 12 Citations |
1 | Integration of QTL and bioinformatic tools to identify candidate genes for triglycerides in mice. (Leduc MS, Hageman RS, Verdugo RA, Tsaih SW, Walsh K, Churchill GA, Paigen B) J Lipid Res 2011 Sep;52(9):1672-82 22 Citations |
1 | Genetic 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 17 Citations |
1 | Refined 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 7 Citations |
1 | Units 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 43 Citations |
1 | Identification 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 11 Citations |
1 | Analyzing 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 41 Citations |
1 | Identifying 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 48 Citations |
1 | Mouse BMD quantitative trait loci show improved concordance with human genome-wide association loci when recalculated on a new, common mouse genetic map. (Ackert-Bicknell CL, Karasik D, Li Q, Smith RV, Hsu YH, Churchill GA, Paigen BJ, Tsaih SW) J Bone Miner Res 2010 Aug;25(8):1808-20 43 Citations |
1 | A survey of airway responsiveness in 36 inbred mouse strains facilitates gene mapping studies and identification of quantitative trait loci. (Leme AS, Berndt A, Williams LK, Tsaih SW, Szatkiewicz JP, Verdugo R, Paigen B, Shapiro SD) Mol Genet Genomics 2010 Apr;283(4):317-26 31 Citations |
1 | Haplotype association mapping in mice. (Tsaih SW, Korstanje R) Methods Mol Biol 2009;573:213-22 17 Citations |
1 | Introgression 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 6 Citations |
1 | Genetic analysis of blood pressure in 8 mouse intercross populations. (Feng M, Deerhake ME, Keating R, Thaisz J, Xu L, Tsaih SW, Smith R, Ishige T, Sugiyama F, Churchill GA, DiPetrillo K) Hypertension 2009 Oct;54(4):802-9 30 Citations |
1 | High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications. (Shaikh TH, Gai X, Perin JC, Glessner JT, Xie H, Murphy K, O'Hara R, Casalunovo T, Conlin LK, D'Arcy M, Frackelton EC, Geiger EA, Haldeman-Englert C, Imielinski M, Kim CE, Medne L, Annaiah K, Bradfield JP, Dabaghyan E, Eckert A, Onyiah CC, Ostapenko S, Otieno FG, Santa E, Shaner JL, Skraban R, Smith RM, Elia J, Goldmuntz E, Spinner NB, Zackai EH, Chiavacci RM, Grundmeier R, Rappaport EF, Grant SF, White PS, Hakonarson H) Genome Res 2009 Sep;19(9):1682-90 307 Citations |
1 | A new standard genetic map for the laboratory mouse. (Cox A, Ackert-Bicknell CL, Dumont BL, Ding Y, Bell JT, Brockmann GA, Wergedal JE, Bult C, Paigen B, Flint J, Tsaih SW, Churchill GA, Broman KW) Genetics 2009 Aug;182(4):1335-44 183 Citations |
1 | Implication 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 14 Citations |
1 | Genome-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 1447 Citations |
1 | Sequence 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 12 Citations |
1 | Congenic 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 16 Citations |
1 | SNP array mapping of chromosome 20p deletions: genotypes, phenotypes, and copy number variation. (Kamath BM, Thiel BD, Gai X, Conlin LK, Munoz PS, Glessner J, Clark D, Warthen DM, Shaikh TH, Mihci E, Piccoli DA, Grant SF, Hakonarson H, Krantz ID, Spinner NB) Hum Mutat 2009 Mar;30(3):371-8 54 Citations |
1 | Genetic 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 7 Citations |
2 | Idd9/11 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 18 Citations |
3 | Chromosome 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 95 Citations |
1 | Refining genetic associations in multiple sclerosis. (International Multiple Sclerosis Genetics Consortium (IMSGC)) Lancet Neurol 2008 Jul;7(7):567-9 84 Citations |
2 | Progress 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):516-22 243 Citations |
1 | Candidate genes for obesity revealed from a C57BL/6J x 129S1/SvImJ intercross. (Su Z, Korstanje R, Tsaih SW, Paigen B) Int J Obes (Lond) 2008 Jul;32(7):1180-9 29 Citations |
1 | Ancestral 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 |
3 | Chromosomal 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 41 Citations |
1 | Genetic analysis of albuminuria in a cross between C57BL/6J and DBA/2J mice. (Sheehan S, Tsaih SW, King BL, Stanton C, Churchill GA, Paigen B, DiPetrillo K) Am J Physiol Renal Physiol 2007 Nov;293(5):F1649-56 37 Citations |
1 | Quantitative trait loci associated with blood pressure of metabolic syndrome in the progeny of NZO/HILtJxC3H/HeJ intercrosses. (Nishihara E, Tsaih SW, Tsukahara C, Langley S, Sheehan S, DiPetrillo K, Kunita S, Yagami K, Churchill GA, Paigen B, Sugiyama F) Mamm Genome 2007 Aug;18(8):573-83 10 Citations |
1 | Expression 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 40 Citations |
1 | A 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 22 Citations |
2 | Multiple 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 63 Citations |
1 | The 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):D658-62 109 Citations |
1 | Introgression 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 |
1 | The genetic dissection of essential hypertension. (Cowley AW Jr) Nat Rev Genet 2006 Nov;7(11):829-40 242 Citations |
1 | Femur mechanical properties in the F2 progeny of an NZB/B1NJ x RF/J cross are regulated predominantly by genetic loci that regulate bone geometry. (Wergedal JE, Ackert-Bicknell CL, Tsaih SW, Sheng MH, Li R, Mohan S, Beamer WG, Churchill GA, Baylink DJ) J Bone Miner Res 2006 Aug;21(8):1256-66 30 Citations |
1 | Linkage disequilibrium mapping in domestic dog breeds narrows the progressive rod-cone degeneration interval and identifies ancestral disease-transmitting chromosome. (Goldstein O, Zangerl B, Pearce-Kelling S, Sidjanin DJ, Kijas JW, Felix J, Acland GM, Aguirre GD) Genomics 2006 Nov;88(5):541-50 63 Citations |
3 | Consomic 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 25 Citations |
1 | A 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 |
1 | Natural 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):577-9 229 Citations |
1 | Genome-wide analysis of core promoter elements from conserved human and mouse orthologous pairs. (Jin VX, Singer GA, Agosto-Pérez FJ, Liyanarachchi S, Davuluri RV) BMC Bioinformatics 2006 Mar 07;7:114 62 Citations |
1 | Impact of genomics on research in the rat. (Lazar J, Moreno C, Jacob HJ, Kwitek AE) Genome Res 2005 Dec;15(12):1717-28 51 Citations |
1 | Genetic counseling issues in urea cycle disorders. (Sniderman King L, Singh RH, Rhead WJ, Smith W, Lee B, Summar ML) Crit Care Clin 2005 Oct;21(4 Suppl):S37-44 20 Citations |
1 | Quantitative trait mapping in a diallel cross of recombinant inbred lines. (Tsaih SW, Lu L, Airey DC, Williams RW, Churchill GA) Mamm Genome 2005 May;16(5):344-55 19 Citations |
1 | Fine 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 |
3 | Genetic 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 14 Citations |
1 | Substitution 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 30 Citations |
1 | Genetic 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 85 Citations |
1 | The 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 49 Citations |
1 | Dimeric 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 48 Citations |
1 | OMGProm: a database of orthologous mammalian gene promoters. (Palaniswamy SK, Jin VX, Sun H, Davuluri RV) Bioinformatics 2005 Mar;21(6):835-6 17 Citations |
2 | Mapping 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 49 Citations |
1 | Consomic rat model systems for physiological genomics. (Cowley AW Jr, Liang M, Roman RJ, Greene AS, Jacob HJ) Acta Physiol Scand 2004 Aug;181(4):585-92 109 Citations |
1 | Integrative 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 19 Citations |
1 | High-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 33 Citations |
1 | Genetic analysis of blood pressure in C3H/HeJ and SWR/J mice. (DiPetrillo K, Tsaih SW, Sheehan S, Johns C, Kelmenson P, Gavras H, Churchill GA, Paigen B) Physiol Genomics 2004 Apr 13;17(2):215-20 48 Citations |
1 | Flagellar 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 51 Citations |
1 | Genetic 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 |
1 | Differential 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 |
1 | Application 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 95 Citations |
1 | Identifying 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 19 Citations |
1 | Genomic 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 87 Citations |
1 | Paradoxical 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 15 Citations |
1 | Serial 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 |
1 | Characterization 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):40-52 122 Citations |
1 | A 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 12 Citations |
1 | The 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 34 Citations |
1 | E 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 8 Citations |
1 | Radiation hybrid map, physical map, and low-pass genomic sequence of the canine prcd region on CFA9 and comparative mapping with the syntenic region on human chromosome 17. (Sidjanin DJ, Miller B, Kijas J, McElwee J, Pillardy J, Malek J, Pai G, Feldblyum T, Fraser C, Acland G, Aguirre G) Genomics 2003 Feb;81(2):138-48 15 Citations |
1 | Genomics and homeostasis. (Cowley AW Jr) Am J Physiol Regul Integr Comp Physiol 2003 Mar;284(3):R611-27 47 Citations |
2 | Identification 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 |
1 | Isotype 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 |
1 | Canine CNGB3 mutations establish cone degeneration as orthologous to the human achromatopsia locus ACHM3. (Sidjanin DJ, Lowe JK, McElwee JL, Milne BS, Phippen TM, Sargan DR, Aguirre GD, Acland GM, Ostrander EA) Hum Mol Genet 2002 Aug 01;11(16):1823-33 173 Citations |
1 | Refinement 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 18 Citations |
1 | Cloning of the canine delta tubulin cDNA (TUBD) and mapping to CFA9. (Sidjanin DJ, Zangerl B, Johnson JL, Xue F, Mellersh C, Ostrander EA, Acland G, Aguirre GD) Anim Genet 2002 Apr;33(2):161-2 3 Citations |
1 | Mapping 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 11 Citations |
1 | A 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):210-4 287 Citations |
1 | IL-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):1509-14 113 Citations |
1 | Rat 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 94 Citations |
1 | A 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):1723-6 152 Citations |
1 | Automated 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 36 Citations |
1 | Cloning of canine gamma-tubulin (TUBG1) cDNA and mapping to CFA9. (Sidjanin DJ, Xue F, McElwee J, Johnson JL, Holmgren C, Mellersh C, Ostrander E, Acland G, Aguirre GD) Anim Genet 2001 Oct;32(5):328-9 2 Citations |
1 | Large 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 91 Citations |
1 | Conformational 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 23 Citations |
1 | A 76-bp deletion in the Mip gene causes autosomal dominant cataract in Hfi mice. (Sidjanin DJ, Parker-Wilson DM, Neuhäuser-Klaus A, Pretsch W, Favor J, Deen PM, Ohtaka-Maruyama C, Lu Y, Bragin A, Skach WR, Chepelinsky AB, Grimes PA, Stambolian DE) Genomics 2001 Jun 15;74(3):313-9 40 Citations |
1 | Positional 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):865-74 215 Citations |
1 | Translocation 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 |
1 | Retinoic 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 55 Citations |
1 | High-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 |
1 | Autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly) is linked to chromosome 22q12-13. (Kelley MJ, Jawien W, Lin A, Hoffmeister K, Pugh EW, Doheny KF, Korczak JF) Hum Genet 2000 May;106(5):557-64 21 Citations |
1 | Clonal 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 18 Citations |
1 | Genomic 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 8 Citations |
1 | Isolation 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 76 Citations |
1 | Appropriate 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 43 Citations |
1 | Molecular 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 |
1 | Detailed 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 |
1 | Psoriasis upregulated phorbolin-1 shares structural but not functional similarity to the mRNA-editing protein apobec-1. (Madsen P, Anant S, Rasmussen HH, Gromov P, Vorum H, Dumanski JP, Tommerup N, Collins JE, Wright CL, Dunham I, MacGinnitie AJ, Davidson NO, Celis JE) J Invest Dermatol 1999 Aug;113(2):162-9 52 Citations |
1 | A 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 186 Citations |
1 | Frequent 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 |
1 | Cloning 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 |
1 | Assignment 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;6(3):251-6 19 Citations |
1 | Mapping 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 31 Citations |
1 | A 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):167-70 348 Citations |
1 | Cloning and chromosomal mapping of the murine norepinephrine transporter. (Fritz JD, Jayanthi LD, Thoreson MA, Blakely RD) J Neurochem 1998 Jun;70(6):2241-51 46 Citations |
1 | A 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 47 Citations |
1 | Mapping of the autosomal dominant cataract mutation (Coc) on mouse chromosome 16. (Sidjanin DJ, Grimes PA, Pretsch W, Neuhäuser-Klaus A, Favor J, Stambolian DE) Invest Ophthalmol Vis Sci 1997 Nov;38(12):2502-7 14 Citations |
1 | Identification 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):7165-8 186 Citations |
1 | Isolation 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):2109-16 173 Citations |
1 | Previously 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 40 Citations |
1 | ExoU 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):547-57 445 Citations |
1 | An 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 31 Citations |
1 | Genetic mapping of a mouse ocular malformation locus, Tcm, to chromosome 4. (Zhou E, Grimes P, Favor J, Koeberlein B, Pretsch W, Neuhauser-Klaus A, Sidjanin D, Stambolian D) Mamm Genome 1997 Mar;8(3):178-81 19 Citations |
1 | Exclusion 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 22 Citations |
1 | PCR-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 |
1 | Evidence 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 34 Citations |
1 | Role 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):22499-505 100 Citations |
1 | Functional 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 |
1 | Persistence 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 68 Citations |
1 | A 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):5520-4 234 Citations |
1 | The 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):1101-7 165 Citations |
1 | Localization 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 |
1 | Differences 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 35 Citations |
1 | Integration 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 |
1 | Liddle'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 1240 Citations |
1 | Linkage 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 10 Citations |
1 | Identification 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):1331-5 197 Citations |
1 | Regional 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 |
1 | Characterization 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 5 Citations |
1 | Linkage 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):392-6 160 Citations |
1 | Clinical 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):524-9 115 Citations |
1 | Alleles 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 |
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1 | Structure, expression, and regulation of the murine renin genes. (Sigmund CD, Gross KW) Hypertension 1991 Oct;18(4):446-57 117 Citations |
1 | Linkage 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 15 Citations |
1 | Organization 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 48 Citations |
1 | An 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 14 Citations |
1 | Dinucleotide repeat polymorphism at the D6S105 locus. (Weber JL, Kwitek AE, May PE, Zoghbi HY) Nucleic Acids Res 1991 Feb 25;19(4):968 65 Citations |
1 | Linkage 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 27 Citations |
1 | Dinucleotide 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 44 Citations |
1 | Dinucleotide 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 62 Citations |
1 | Dinucleotide 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 38 Citations |
1 | Dinucleotide 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 34 Citations |
1 | Dinucleotide repeat polymorphisms at the D11S419 and CD3D loci. (Weber JL, Kwitek AE, May PE) Nucleic Acids Res 1990 Jul 11;18(13):4036 30 Citations |
1 | Dinucleotide repeat polymorphisms at the D7S435 and D7S440 loci. (Weber JL, Kwitek AE, May PE) Nucleic Acids Res 1990 Jul 11;18(13):4039 39 Citations |
1 | Dinucleotide repeat polymorphism at the D1S103 locus. (Weber JL, Kwitek AE, May PE) Nucleic Acids Res 1990 Apr 25;18(8):2199 |
1 | Dinucleotide repeat polymorphism at the D1S102 locus. (Weber JL, Kwitek AE, May PE) Nucleic Acids Res 1990 Apr 25;18(8):2199 25 Citations |
1 | Philadelphia-negative chronic myelogenous leukemia with breakpoint cluster region rearrangement: molecular analysis, clinical characteristics, and response to therapy. (Shtalrid M, Talpaz M, Blick M, Romero P, Kantarjian H, Taylor K, Trujillo J, Schachner J, Gutterman JU, Kurzrock R) J Clin Oncol 1988 Oct;6(10):1569-75 42 Citations |
1 | Analysis of breakpoints within the bcr gene and their correlation with the clinical course of Philadelphia-positive chronic myelogenous leukemia. (Shtalrid M, Talpaz M, Kurzrock R, Kantarjian H, Trujillo J, Gutterman J, Yoffe G, Blick M) Blood 1988 Aug;72(2):485-90 113 Citations |
1 | Molecular analysis of chromosome 22 breakpoints in adult Philadelphia-positive acute lymphoblastic leukaemia. (Kurzrock R, Shtalrid M, Gutterman JU, Koller CA, Walters R, Trujillo JM, Talpaz M) Br J Haematol 1987 Sep;67(1):55-9 29 Citations |
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