Genetic analysis for common complex disease : Genetics of coronary heart disease: Current understanding and future prospectsHAUSER, Elizabeth R; PERICAK-VANCE, Margaret A.The American heart journal. 2000, Vol 140, Num 4, pp S36-S44, issn 0002-8703Article

Genotype at Polymorphism rs1 1200638 and HTRA1 Expression LevelGAOFENG WANG; SCOTT, William K; HAINES, Jonathan L et al.Archives of ophthalmology (1960). 2010, Vol 128, Num 11, pp 1491-1493, issn 0003-9950, 3 p.Article

No gene is an Island : The flip-flop phenomenonLIN, Ping-I; VANCE, Jeffery M; PERICAK-VANCE, Margaret A et al.American journal of human genetics. 2007, Vol 80, Num 3, pp 531-538, issn 0002-9297, 8 p.Article

Genome-wide Linkage Scan in Fuchs Endothelial Corneal DystrophyAFSHARI, Natalie A; LI, Yi-Ju; PERICAK-VANCE, Margaret A et al.Investigative ophthalmology & visual science. 2009, Vol 50, Num 3, pp 1093-1097, issn 0146-0404, 5 p.Article

Lewy body pathology is a frequent co-pathology in familial Alzheimer's diseaseTREMBATH, Yuri; ROSENBERG, Carolyn; ERVIN, John F et al.Acta neuropathologica. 2003, Vol 105, Num 5, pp 484-488, issn 0001-6322, 5 p.Article

GAW 8 : genetic analysis workshopELSTON, Robert C; SPENCE, M. Anne; HAINES, Jonathan et al.Genetic epidemiology. 1993, Vol 10, Num 6, issn 0741-0395Conference Proceedings

Resolving the relationship between ApolipoproteinE and depressionSLIFER, Michael A; MARTIN, Eden R; GILBERT, John R et al.Neuroscience letters. 2009, Vol 455, Num 2, pp 116-119, issn 0304-3940, 4 p.Article

Identification of risk and age-at-onset genes on chromosome 1p in parkinson diseaseOLIVEIRA, Sofia A; LI, Yi-Ju; NOUREDDINE, Maher A et al.American journal of human genetics. 2005, Vol 77, Num 2, pp 252-264, issn 0002-9297, 13 p.Article

Migraine with aura susceptibility locus on chromosome 19p13 is distinct from the familial hemiplegic migraine locusJONES, Keith W; EHM, Margaret G; PERICAK-VANCE, Margaret A et al.Genomics (San Diego, Calif.). 2001, Vol 78, Num 3, pp 150-154, issn 0888-7543Article

Identification of two novel loci for dominantly inherited familial amyotrophic lateral sclerosisSAPP, Peter C; HOSLER, Betsy A; VALESKY, Marianne et al.American journal of human genetics. 2003, Vol 73, Num 2, pp 397-403, issn 0002-9297, 7 p.Article

The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosisYI YANG; HENTATI, Afif; COLE, Natalie et al.Nature genetics. 2001, Vol 29, Num 2, pp 160-165, issn 1061-4036Article

Recruiting Intergenerational African American Males for Biomedical Research Studies: A Major Research ChallengeBYRD, Goldie S; EDWARDS, Christopher L; PERICAK-VANCE, Margaret et al.Journal of the National Medical Association. 2011, Vol 103, Num 6, pp 480-487, issn 0027-9684, 8 p.Article

A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHCDE BAKKER, Paul I. W; MCVEAN, Gil; MORRISON, Jonathan et al.Nature genetics. 2006, Vol 38, Num 10, pp 1166-1172, issn 1061-4036, 7 p.Article

Thrombotic Storm Revisited: Preliminary Diagnostic Criteria Suggested by the Thrombotic Storm Study GroupKITCHENS, Craig S; ERKAN, Doruk; BRANDAO, Leonardo R et al.The American journal of medicine. 2011, Vol 124, Num 4, pp 290-296, issn 0002-9343, 7 p.Article

REEPI mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31BEETZ, Christian; SCHÜLE, Rebecca; NYGREN, Anders O. H et al.Brain. 2008, Vol 131, pp 1078-1086, issn 0006-8950, 9 p., 4Article

Evidence against a role for rare ADAM10 mutations in sporadic Alzheimer DiseaseGUIQING CAI; ATZMON, Gil; NAJ, Adam C et al.Neurobiology of aging. 2012, Vol 33, Num 2, pp 416-417, issn 0197-4580, 2 p.Article

Notch activation induces endothelial cell senescence and pro-inflammatory response: Implication of Notch signaling in atherosclerosisLIU, Zhao-Jun; YURONG TAN; LIVINGSTONE, Alan S et al.Atherosclerosis. 2012, Vol 225, Num 2, pp 296-303, issn 0021-9150, 8 p.Article

Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factorBAN, Maria; GORIS, An; DUBOIS, Bénédicte et al.European journal of human genetics. 2009, Vol 17, Num 10, pp 1309-1313, issn 1018-4813, 5 p.Article

A conserved sorting-associated protein is mutant in chorea-acanthocytosisRAMPOLDI, Luca; DOBSON-STONE, Carol; BROWN, Robert et al.Nature genetics. 2001, Vol 28, Num 2, pp 119-120, issn 1061-4036Article

Exploring the Relationship Between Autism Spectrum Disorder and Epilepsy Using Latent Class Cluster AnalysisCUCCARO, Michael L; TUCHMAN, Roberto F; HAMILTON, Kara L et al.Journal of autism and developmental disorders. 2012, Vol 42, Num 8, pp 1630-1641, issn 0162-3257, 12 p.Article

A genome-wide search for linkage to asthma phenotypes in the genetics of asthma international network families : evidence for a major susceptibility locus on chromosome 2pPILLAI, Sreekumar G; CHIANO, Mathias N; SLY, Peter et al.European journal of human genetics. 2006, Vol 14, Num 3, pp 307-316, issn 1018-4813, 10 p.Article

PTPRC (CD45) is not associated with the development of multiple sclerosis in U.S. patientsBARCELLOS, Lisa F; CAILLIER, Stacy; HAUSER, Stephen L et al.Nature genetics. 2001, Vol 29, Num 1, pp 23-24, issn 1061-4036Article

Genome-wide Association Study Implicates a Chromosome 12 Risk Locus for Late-Onset Alzheimer DiseaseBEECHAM, Gary W; MARTIN, Eden R; LI, Yi-Ju et al.American journal of human genetics. 2009, Vol 84, Num 1, pp 35-43, issn 0002-9297, 9 p.Article

C3 R102G polymorphism increases risk of age-related macular degenerationSPENCER, Kylee L; OLSON, Lana M; ANDERSON, Brent M et al.Human molecular genetics (Print). 2008, Vol 17, Num 12, pp 1821-1824, issn 0964-6906, 4 p.Article

Distribution of WDR36 DNA sequence variants in patients with primary open-angle glaucomaHAUSER, Michael A; RAND ALLINGHAM, R; WIGGS, Janey L et al.Investigative ophthalmology & visual science. 2006, Vol 47, Num 6, pp 2542-2546, issn 0146-0404, 5 p.Article