| 2 | Chromosomal Substitution Strategies to Localize Genomic Regions Related to Complex Traits. (Cowley AW Jr, Dwinell MR) Compr Physiol 2020 Mar 12;10(2):365-388 7 Citations |
| 1 | Extrusion pump ABCC1 was first linked with nonsyndromic hearing loss in humans by stepwise genetic analysis. (Li M, Mei L, He C, Chen H, Cai X, Liu Y, Tian R, Tian Q, Song J, Jiang L, Liu C, Wu H, Li T, Liu J, Li X, Yi Y, Yan D, Blanton SH, Hu Z, Liu X, Li J, Ling J, Feng Y) Genet Med 2019 Dec;21(12):2744-2754 31 Citations |
| 1 | The impact of the UGT1A1*60 allele on bilirubin serum concentrations. (Pasternak AL, Crews KR, Caudle KE, Smith C, Pei D, Cheng C, Broeckel U, Gaur AH, Hankins J, Relling MV, Haidar CE) Pharmacogenomics 2017 Jan;18(1):5-16 6 Citations |
| 1 | De novo RRAGC mutation activates mTORC1 signaling in syndromic fetal dilated cardiomyopathy. (Long PA, Zimmermann MT, Kim M, Evans JM, Xu X, Olson TM) Hum Genet 2016 Aug;135(8):909-917 32 Citations |
| 1 | The kdr-bearing haplotype and susceptibility to Plasmodium falciparum in Anopheles gambiae: genetic correlation and functional testing. (Mitri C, Markianos K, Guelbeogo WM, Bischoff E, Gneme A, Eiglmeier K, Holm I, Sagnon N, Vernick KD, Riehle MM) Malar J 2015 Oct 06;14:391 37 Citations |
| 2 | High HLA-DP Expression and Graft-versus-Host Disease. (Petersdorf EW, Malkki M, O'hUigin C, Carrington M, Gooley T, Haagenson MD, Horowitz MM, Spellman SR, Wang T, Stevenson P) N Engl J Med 2015 Aug 13;373(7):599-609 253 Citations |
| 1 | Conserved genetic pathways associated with microphthalmia, anophthalmia, and coloboma. (Reis LM, Semina EV) Birth Defects Res C Embryo Today 2015 Jun;105(2):96-113 69 Citations |
| 1 | Expression quantitative trait loci and receptor pharmacology implicate Arg1 and the GABA-A receptor as therapeutic targets in neuroblastoma. (Hackett CS, Quigley DA, Wong RA, Chen J, Cheng C, Song YK, Wei JS, Pawlikowska L, Bao Y, Goldenberg DD, Nguyen K, Gustafson WC, Rallapalli SK, Cho YJ, Cook JM, Kozlov S, Mao JH, Van Dyke T, Kwok PY, Khan J, Balmain A, Fan Q, Weiss WA) Cell Rep 2014 Nov 06;9(3):1034-46 32 Citations |
| 1 | A novel variant in CDKN1C is associated with intrauterine growth restriction, short stature, and early-adulthood-onset diabetes. (Kerns SL, Guevara-Aguirre J, Andrew S, Geng J, Guevara C, Guevara-Aguirre M, Guo M, Oddoux C, Shen Y, Zurita A, Rosenfeld RG, Ostrer H, Hwa V, Dauber A) J Clin Endocrinol Metab 2014 Oct;99(10):E2117-22 53 Citations |
| 1 | Genetic susceptibility and loss of Nr4a1 enhances macrophage-mediated renal injury in CKD. (Westbrook L, Johnson AC, Regner KR, Williams JM, Mattson DL, Kyle PB, Henegar JR, Garrett MR) J Am Soc Nephrol 2014 Nov;25(11):2499-510 43 Citations |
| 2 | Genetic control of murine invariant natural killer T cells maps to multiple type 1 diabetes regions. (Tsaih SW, Khaja S, Ciecko AE, MacKinney E, Chen YG) Genes Immun 2013 Sep;14(6):380-6 4 Citations |
| 1 | Ultra-rare mutation in long-range enhancer predisposes to thyroid carcinoma with high penetrance. (He H, Li W, Wu D, Nagy R, Liyanarachchi S, Akagi K, Jendrzejewski J, Jiao H, Hoag K, Wen B, Srinivas M, Waidyaratne G, Wang R, Wojcicka A, Lattimer IR, Stachlewska E, Czetwertynska M, Dlugosinska J, Gierlikowski W, Ploski R, Krawczyk M, Jazdzewski K, Kere J, Symer DE, Jin V, Wang Q, de la Chapelle A) PLoS One 2013;8(5):e61920 41 Citations |
| 1 | QTL-based association analyses reveal novel genes influencing pleiotropy of metabolic syndrome (MetS). (Zhang Y, Kent JW Jr, Olivier M, Ali O, Broeckel U, Abdou RM, Dyer TD, Comuzzie A, Curran JE, Carless MA, Rainwater DL, Göring HH, Blangero J, Kissebah AH) Obesity (Silver Spring) 2013 Oct;21(10):2099-111 14 Citations |
| 1 | Dynamic genetic linkage of intermediate blood pressure phenotypes during postural adaptations in a founder population. (Arenas IA, Tremblay J, Deslauriers B, Sandoval J, Šeda O, Gaudet D, Merlo E, Kotchen T, Cowley AW Jr, Hamet P) Physiol Genomics 2013 Feb 15;45(4):138-50 7 Citations |
| 1 | Predicting disease-related subnetworks for type 1 diabetes using a new network activity score. (Gao S, Jia S, Hessner MJ, Wang X) OMICS 2012 Oct;16(10):566-78 10 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 | Increased susceptibility to kidney injury by transfer of genomic segment from SHR onto Dahl S genetic background. (Regner KR, Harmon AC, Williams JM, Stelloh C, Johnson AC, Kyle PB, Lerch-Gaggl A, White SM, Garrett MR) Physiol Genomics 2012 Jun 15;44(12):629-37 16 Citations |
| 1 | Obesity-insulin targeted genes in the 3p26-25 region in human studies and LG/J and SM/J mice. (Kraja AT, Lawson HA, Arnett DK, Borecki IB, Broeckel U, de las Fuentes L, Hunt SC, Province MA, Cheverud J, Rao DC) Metabolism 2012 Aug;61(8):1129-41 11 Citations |
| 1 | Mutations in the β subunit of RNA polymerase alter intrinsic cephalosporin resistance in Enterococci. (Kristich CJ, Little JL) Antimicrob Agents Chemother 2012 Apr;56(4):2022-7 38 Citations |
| 1 | Unmasking genes in a type 1 diabetes-resistant mouse strain that enhances pathogenic CD8 T-cell responses. (Driver JP, Chen YG, Zhang W, Asrat S, Serreze DV) Diabetes 2011 Apr;60(4):1354-9 6 Citations |
| 1 | Linkage mapping of principal components for femoral biomechanical performance in a reciprocal HCB-8 × HCB-23 intercross. (Saless N, Litscher SJ, Vanderby R, Demant P, Blank RD) Bone 2011 Mar 01;48(3):647-53 15 Citations |
| 1 | Introduction to genetics and childhood obesity: relevance to nursing practice. (Seal N) Biol Res Nurs 2011 Jan;13(1):61-9 6 Citations |
| 1 | Novel genetic variants contributing to left ventricular hypertrophy: the HyperGEN study. (Arnett DK, Devereux RB, Rao DC, Li N, Tang W, Kraemer R, Claas SA, Leon JM, Broeckel U) J Hypertens 2009 Aug;27(8):1585-93 31 Citations |
| 1 | A novel locus for adolescent idiopathic scoliosis on chromosome 12p. (Raggio CL, Giampietro PF, Dobrin S, Zhao C, Dorshorst D, Ghebranious N, Weber JL, Blank RD) J Orthop Res 2009 Oct;27(10):1366-72 49 Citations |
| 1 | Genetic determinants of hypertension: an update. (Harrison M, Maresso K, Broeckel U) Curr Hypertens Rep 2008 Dec;10(6):488-95 31 Citations |
| 1 | Genetically hypertensive Brown Norway congenic rat strains suggest intermediate traits underlying genetic hypertension. (Bilusić M, Moreno C, Barreto NE, Tschannen MR, Harris EL, Porteous WK, Thompson CM, Grigor MR, Weder A, Boerwinkle E, Hunt SC, Curb JD, Jacob HJ, Kwitek AE) Croat Med J 2008 Oct;49(5):586-99 8 Citations |
| 1 | Linkage of Crohn's disease-related serological phenotypes: NFKB1 haplotypes are associated with anti-CBir1 and ASCA, and show reduced NF-kappaB activation. (Takedatsu H, Taylor KD, Mei L, McGovern DP, Landers CJ, Gonsky R, Cong Y, Vasiliauskas EA, Ippoliti A, Elson CO, Rotter JI, Targan SR) Gut 2009 Jan;58(1):60-7 24 Citations |
| 1 | Refining genetic associations in multiple sclerosis. (International Multiple Sclerosis Genetics Consortium (IMSGC)) Lancet Neurol 2008 Jul;7(7):567-9 85 Citations |
| 1 | A case of true hermaphroditism reveals an unusual mechanism of twinning. (Souter VL, Parisi MA, Nyholt DR, Kapur RP, Henders AK, Opheim KE, Gunther DF, Mitchell ME, Glass IA, Montgomery GW) Hum Genet 2007 Apr;121(2):179-85 43 Citations |
| 1 | Linkage analysis for complex diseases using variance component analysis: SOLAR. (Broeckel U, Maresso K, Martin LJ) Methods Mol Med 2006;128:91-100 2 Citations |
| 1 | The genetic dissection of essential hypertension. (Cowley AW Jr) Nat Rev Genet 2006 Nov;7(11):829-40 246 Citations |
| 1 | Association between the C3435T polymorphism of the MDR1 gene and Crohn's disease. (Lal S, Stempak JM, Law C, Elkadri AA, Steinhart AH, Silverberg MS) Inflamm Bowel Dis 2006 Oct;12(10):1006-7 6 Citations |
| 1 | Application of genetic approaches to ocular disease. (Ruttum MS, Reis LM, Semina EV) Pediatr Clin North Am 2006 Aug;53(4):751-65 1 Citation |
| 1 | Molecular and cellular pathophysiology of autosomal recessive polycystic kidney disease (ARPKD). (Sweeney WE Jr, Avner ED) Cell Tissue Res 2006 Dec;326(3):671-85 102 Citations |
| 1 | Radiation hybrid mapping of cataract genes in the dog. (Hunter LS, Sidjanin DJ, Johnson JL, Zangerl B, Galibert F, Andre C, Kirkness E, Talamas E, Acland GM, Aguirre GD) Mol Vis 2006 May 24;12:588-96 9 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):577-9 231 Citations |
| 1 | Fine mapping of Lvm1: a quantitative trait locus controlling heart size independently of blood pressure. (Di Nicolantonio R, Kostka V, Kwitek A, Jacob H, Thomas WG, Harrap SB) Pulm Pharmacol Ther 2006;19(1):70-3 6 Citations |
| 2 | Quantitative founder-effect analysis of French Canadian families identifies specific loci contributing to metabolic phenotypes of hypertension. (Hamet P, Merlo E, Seda O, Broeckel U, Tremblay J, Kaldunski M, Gaudet D, Bouchard G, Deslauriers B, Gagnon F, Antoniol G, Pausová Z, Labuda M, Jomphe M, Gossard F, Tremblay G, Kirova R, Tonellato P, Orlov SN, Pintos J, Platko J, Hudson TJ, Rioux JD, Kotchen TA, Cowley AW Jr) Am J Hum Genet 2005 May;76(5):815-32 72 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 50 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):585-92 110 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 10 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 99 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 88 Citations |
| 1 | Mutations in the amino terminus of ANKH in two US families with calcium pyrophosphate dihydrate crystal deposition disease. (Williams CJ, Pendleton A, Bonavita G, Reginato AJ, Hughes AE, Peariso S, Doherty M, McCarty DJ, Ryan LM) Arthritis Rheum 2003 Sep;48(9):2627-31 66 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 | X-linked lymphoproliferative disease: genetic lesions and clinical consequences. (MacGinnitie AJ, Geha R) Curr Allergy Asthma Rep 2002 Sep;2(5):361-7 10 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):1823-33 176 Citations |
| 1 | Structural characterization of Rasgrf1 and a novel linked imprinted locus. (de la Puente A, Hall J, Wu YZ, Leone G, Peters J, Yoon BJ, Soloway P, Plass C) Gene 2002 May 29;291(1-2):287-97 31 Citations |
| 1 | A meta-analytic investigation of linkage and association of common leptin receptor (LEPR) polymorphisms with body mass index and waist circumference. (Heo M, Leibel RL, Fontaine KR, Boyer BB, Chung WK, Koulu M, Karvonen MK, Pesonen U, Rissanen A, Laakso M, Uusitupa MI, Chagnon Y, Bouchard C, Donohoue PA, Burns TL, Shuldiner AR, Silver K, Andersen RE, Pedersen O, Echwald S, Sørensen TI, Behn P, Permutt MA, Jacobs KB, Elston RC, Hoffman DJ, Gropp E, Allison DB) Int J Obes Relat Metab Disord 2002 May;26(5):640-6 112 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):210-4 294 Citations |
| 1 | Bietti crystalline retinopathy and juvenile retinoschisis in a family with a novel RS1 mutation. (Weinberg DV, Sieving PA, Bingham EL, Jampol LM, Mets MB) Arch Ophthalmol 2001 Nov;119(11):1719-21 5 Citations |
| 1 | The genetic basis of plasma variation in adiponectin, a global endophenotype for obesity and the metabolic syndrome. (Comuzzie AG, Funahashi T, Sonnenberg G, Martin LJ, Jacob HJ, Black AE, Maas D, Takahashi M, Kihara S, Tanaka S, Matsuzawa Y, Blangero J, Cohen D, Kissebah A) J Clin Endocrinol Metab 2001 Sep;86(9):4321-5 290 Citations |
| 1 | Breaking down bone strength: a perspective on the future of skeletal genetics. (Blank RD) J Bone Miner Res 2001 Jul;16(7):1207-11 20 Citations |
| 1 | Bone strength and related traits in HcB/Dem recombinant congenic mice. (Yershov Y, Baldini TH, Villagomez S, Young T, Martin ML, Bockman RS, Peterson MG, Blank RD) J Bone Miner Res 2001 Jun;16(6):992-1003 41 Citations |
| 1 | Linkage and candidate gene analysis of autosomal-dominant familial exudative vitreoretinopathy. (Shastry BS, Hejtmancik JF, Hiraoka M, Ibaraki N, Okubo Y, Okubo A, Han DP, Trese MT) Clin Genet 2000 Oct;58(4):329-32 17 Citations |
| 1 | The future of genetic case-control studies. (Schork NJ, Fallin D, Thiel B, Xu X, Broeckel U, Jacob HJ, Cohen D) Adv Genet 2001;42:191-212 90 Citations |
| 1 | Genetically defined risk of salt sensitivity in an intercross of Brown Norway and Dahl S rats. (Cowley AW Jr, Stoll M, Greene AS, Kaldunski ML, Roman RJ, Tonellato PJ, Schork NJ, Dumas P, Jacob HJ) Physiol Genomics 2000 Apr 27;2(3):107-15 72 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 | Deletion in the promoter region and altered expression of Pitx3 homeobox gene in aphakia mice. (Semina EV, Murray JC, Reiter R, Hrstka RF, Graw J) Hum Mol Genet 2000 Jul 01;9(11):1575-85 170 Citations |
| 1 | Split-hand/split-foot malformation is caused by mutations in the p63 gene on 3q27. (Ianakiev P, Kilpatrick MW, Toudjarska I, Basel D, Beighton P, Tsipouras P) Am J Hum Genet 2000 Jul;67(1):59-66 242 Citations |
| 1 | Atypical clustering of gynecologic malignancies: A family study including molecular analysis of candidate genes. (Cohn DE, Babb S, Whelan AJ, Mutch DG, Herzog TJ, Rader JS, Elbendary A, Goodfellow PJ) Gynecol Oncol 2000 Apr;77(1):18-25 10 Citations |
| 1 | Genomic organization of the KIAA0057 gene that encodes a TRAM-like protein and its exclusion as a polycystic kidney and hepatic disease 1 (PKHD1) candidate gene. (Onuchic LF, Mrug M, Lakings AL, Muecher G, Becker J, Zerres K, Avner ED, Dixit M, Somlo S, Germino GG, Guay-Woodford LM) Mamm Genome 1999 Dec;10(12):1175-8 8 Citations |
| 1 | Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence change. (Hiriyanna KT, Bingham EL, Yashar BM, Ayyagari R, Fishman G, Small KW, Weinberg DV, Weleber RG, Lewis RA, Andreasson S, Richards JE, Sieving PA) Hum Mutat 1999;14(5):423-7 44 Citations |
| 1 | A genomic approach to scoliosis pathogenesis. (Blank RD, Raggio CL, Giampietro PF, Camacho NP) Lupus 1999;8(5):356-60 19 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 187 Citations |
| 1 | Linkage, association, and the genetic analysis of bone mineral density and related phenotypes: an overview for clinicians. (Blank RD) J Clin Densitom 1999;2(1):59-70 1 Citation |
| 1 | ERGIC-53 gene structure and mutation analysis in 19 combined factors V and VIII deficiency families. (Nichols WC, Terry VH, Wheatley MA, Yang A, Zivelin A, Ciavarella N, Stefanile C, Matsushita T, Saito H, de Bosch NB, Ruiz-Saez A, Torres A, Thompson AR, Feinstein DI, White GC, Negrier C, Vinciguerra C, Aktan M, Kaufman RJ, Ginsburg D, Seligsohn U) Blood 1999 Apr 01;93(7):2261-6 77 Citations |
| 1 | Clinical and functional effects of mutations in the DAX-1 gene in patients with adrenal hypoplasia congenita. (Reutens AT, Achermann JC, Ito M, Ito M, Gu WX, Habiby RL, Donohoue PA, Pang S, Hindmarsh PC, Jameson JL) J Clin Endocrinol Metab 1999 Feb;84(2):504-11 168 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 | CLCN5 chloride-channel mutations in six new North American families with X-linked nephrolithiasis. (Hoopes RR Jr, Hueber PA, Reid RJ Jr, Braden GL, Goodyer PR, Melnyk AR, Midgley JP, Moel DI, Neu AM, VanWhy SK, Scheinman SJ) Kidney Int 1998 Sep;54(3):698-705 61 Citations |
| 1 | Usher syndrome in the Samaritans: strengths and limitations of using inbred isolated populations to identify genes causing recessive disorders. (Bonné-Tamir B, Nystuen A, Seroussi E, Kalinsky H, Kwitek-Black AE, Korostishevsky M, Adato A, Sheffield VC) Am J Phys Anthropol 1997 Oct;104(2):193-200 12 Citations |
| 1 | Linkage 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 31 Citations |
| 1 | Linkage of autosomal dominant iris hypoplasia to the region of the Rieger syndrome locus (4q25). (Héon E, Sheth BP, Kalenak JW, Sunden SL, Streb LM, Taylor CM, Alward WL, Sheffield VC, Stone EM) Hum Mol Genet 1995 Aug;4(8):1435-9 61 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):1101-7 166 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 1258 Citations |
| 1 | Gene time for polycystic kidney disease. (Avner ED) Lancet 1994 Sep 24;344(8926):833-4 3 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):1331-5 199 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):392-6 161 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):524-9 117 Citations |
| 1 | Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4. (Murray JC, Bennett SR, Kwitek AE, Small KW, Schinzel A, Alward WL, Weber JL, Bell GI, Buetow KH) Nat Genet 1992 Sep;2(1):46-9 |
| 1 | Mapping 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 93 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 | Mouse chromosome 4. (Blank R, Eppig J, Fiedorek FT Jr, Frankel WN, Friedman JM, Huppi K, Jackson I, Mock B) Mamm Genome 1991;1 Spec No:S51-78 15 Citations |
| 1 | A linkage map of mouse chromosome 12: localization of Igh and effects of sex and interference on recombination. (Blank RD, Campbell GR, Calabro A, D'Eustachio P) Genetics 1988 Dec;120(4):1073-83 70 Citations |
| 1 | Association and linkage studies of immunoglobulin heavy chain allotypes in inflammatory bowel disease. (Gudjonsson H, Schanfield MS, Albertini RJ, McAuliffe TL, Beeken WL, Krawitt EL) Tissue Antigens 1988 May;31(5):243-9 6 Citations |
| 1 | Bayesian multilocus linkage mapping. (Blank RD, Campbell GR, Pollak M, D'Eustachio P) Curr Top Microbiol Immunol 1988;137:25-32 |
| 1 | Hereditary proximal spinal and bulbar motor neuron disease of late onset. A report of six cases. (Barkhaus PE, Kennedy WR, Stern LZ, Harrington RB) Arch Neurol 1982 Feb;39(2):112-6 36 Citations |
| 1 | Genetic susceptibility to multiple sclerosis: a linkage analysis with age-of-onset corrections. (Haile RW, Hodge SE, Visscher BR, Spence MA, Detels R, McAuliffe TL, Park MS, Dudley JP) Clin Genet 1980 Sep;18(3):160-7 20 Citations |
