Targeted resequencing implicates the familial Mediterranean fever gene MEFV and the toll-like receptor 4 gene TLR4 in Behçet disease
Kirino, Yohei, Zhou, Qing, Ishigatsubo, Yoshiaki, Mizuki, Nobuhisa, Tugal-Tutkun, Ilknur, Seyahi, Emire, Özyazgan, Yilmaz, Ugurlu, Serdal, Erer, Burak, Abaci, Neslihan, Ustek, Duran, Meguro, Akira, Ueda, Atsuhisa, Takeno, Mitsuhiro, Inoko, Hidetoshi, Ombrello, Michael J., Satorius, Colleen L., Maskeri, Baishali, Mullikin, James C., Sun, Hong-Wei, Gutierrez-Cruz, Gustavo, Kim, Yoonhee, Wilson, Alexander F., Kastner, Daniel L., Gül, Ahmet, Remmers, Elaine F.
Published in Proceedings of the National Academy of Sciences - PNAS (14.05.2013)
Published in Proceedings of the National Academy of Sciences - PNAS (14.05.2013)
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Gene‐level association analysis of bivariate ordinal traits with functional regressions
Wang, Shuqi, Chiu, Chi‐Yang, Wilson, Alexander F., Bailey‐Wilson, Joan E., Agron, Elvira, Chew, Emily Y., Ahn, Jaeil, Xiong, Momiao, Fan, Ruzong
Published in Genetic epidemiology (01.09.2023)
Published in Genetic epidemiology (01.09.2023)
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The ClinSeq Project: piloting large-scale genome sequencing for research in genomic medicine
Biesecker, Leslie G, Mullikin, James C, Facio, Flavia M, Turner, Clesson, Cherukuri, Praveen F, Blakesley, Robert W, Bouffard, Gerard G, Chines, Peter S, Cruz, Pedro, Hansen, Nancy F, Teer, Jamie K, Maskeri, Baishali, Young, Alice C, Manolio, Teri A, Wilson, Alexander F, Finkel, Toren, Hwang, Paul, Arai, Andrew, Remaley, Alan T, Sachdev, Vandana, Shamburek, Robert, Cannon, Richard O, Green, Eric D
Published in Genome Research (01.09.2009)
Published in Genome Research (01.09.2009)
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The FKBP5 -Gene in Depression and Treatment Response—an Association Study in the Sequenced Treatment Alternatives to Relieve Depression (STARD) Cohort
Lekman, Magnus, Laje, Gonzalo, Charney, Dennis, Rush, A. John, Wilson, Alexander F, Sorant, Alexa J.M, Lipsky, Robert, Wisniewski, Stephen R, Manji, Husseini, McMahon, Francis J, Paddock, Silvia
Published in Biological psychiatry (1969) (15.06.2008)
Published in Biological psychiatry (1969) (15.06.2008)
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Genetic Markers of Suicidal Ideation Emerging During Citalopram Treatment of Major Depression
Laje, Gonzalo, Paddock, Silvia, Manji, Husseini, Rush, A. John, Wilson, Alexander F., Charney, Dennis, McMahon, Francis J.
Published in The American journal of psychiatry (01.10.2007)
Published in The American journal of psychiatry (01.10.2007)
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A Common Polymorphism in HIBCH Influences Methylmalonic Acid Concentrations in Blood Independently of Cobalamin
Molloy, Anne M., Pangilinan, Faith, Mills, James L., Shane, Barry, O’Neill, Mary B., McGaughey, David M., Velkova, Aneliya, Abaan, Hatice Ozel, Ueland, Per M., McNulty, Helene, Ward, Mary, Strain, J.J., Cunningham, Conal, Casey, Miriam, Cropp, Cheryl D., Kim, Yoonhee, Bailey-Wilson, Joan E., Wilson, Alexander F., Brody, Lawrence C.
Published in American journal of human genetics (05.05.2016)
Published in American journal of human genetics (05.05.2016)
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Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association
Desch, Karl C., Ozel, Ayse B., Siemieniak, David, Kalish, Yossi, Shavit, Jordan A., Thornburg, Courtney D., Sharathkumar, Anjali A., McHugh, Caitlin P., Laurie, Cathy C., Crenshaw, Andrew, Mirel, Daniel B., Kim, Yoonhee, Cropp, Cheryl D., Molloy, Anne M., Kirke, Peadar N., Bailey-Wilson, Joan E., Wilson, Alexander F., Mills, James L., Scott, John M., Brody, Lawrence C., Li, Jun Z., Ginsburg, David
Published in Proceedings of the National Academy of Sciences - PNAS (08.01.2013)
Published in Proceedings of the National Academy of Sciences - PNAS (08.01.2013)
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Targeted deep resequencing identifies coding variants in the PEAR1 gene that play a role in platelet aggregation
Kim, Yoonhee, Suktitipat, Bhoom, Yanek, Lisa R, Faraday, Nauder, Wilson, Alexander F, Becker, Diane M, Becker, Lewis C, Mathias, Rasika A
Published in PloS one (21.05.2013)
Published in PloS one (21.05.2013)
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Identification of candidate regions for familial idiopathic scoliosis
Miller, Nancy H, Justice, Cristina M, Marosy, Beth, Doheny, Kimberly F, Pugh, Elizabeth, Zhang, Jun, Dietz, 3rd, Harry C, Wilson, Alexander F
Published in Spine (Philadelphia, Pa. 1976) (15.05.2005)
Published in Spine (Philadelphia, Pa. 1976) (15.05.2005)
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Genetic modifiers of neurofibromatosis type 1-associated café-au-lait macule count identified using multi-platform analysis
Pemov, Alexander, Sung, Heejong, Hyland, Paula L, Sloan, Jennifer L, Ruppert, Sarah L, Baldwin, Andrea M, Boland, Joseph F, Bass, Sara E, Lee, Hyo Jung, Jones, Kristine M, Zhang, Xijun, Mullikin, James C, Widemann, Brigitte C, Wilson, Alexander F, Stewart, Douglas R
Published in PLoS genetics (01.10.2014)
Published in PLoS genetics (01.10.2014)
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Genome‐wide association study of café‐au‐lait macule number in neurofibromatosis type 1
Sung, Heejong, Hyland, Paula L., Pemov, Alexander, Sabourin, Jeremy A., Baldwin, Andrea M., Bass, Sara, Teshome, Kedest, Luo, Wen, Widemann, Brigitte C., Stewart, Douglas R., Wilson, Alexander F.
Published in Molecular genetics & genomic medicine (01.10.2020)
Published in Molecular genetics & genomic medicine (01.10.2020)
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Evaluation of IRX Genes and Conserved Noncoding Elements in a Region on 5p13.3 Linked to Families with Familial Idiopathic Scoliosis and Kyphosis
Justice, Cristina M, Bishop, Kevin, Carrington, Blake, Mullikin, Jim C, Swindle, Kandice, Marosy, Beth, Sood, Raman, Miller, Nancy H, Wilson, Alexander F
Published in G3 : genes - genomes - genetics (01.06.2016)
Published in G3 : genes - genomes - genetics (01.06.2016)
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A combined genome-wide linkage and association approach to find susceptibility loci for platelet function phenotypes in European American and African American families with coronary artery disease
Mathias, Rasika A, Kim, Yoonhee, Sung, Heejong, Yanek, Lisa R, Mantese, V J, Hererra-Galeano, J Enrique, Ruczinski, Ingo, Wilson, Alexander F, Faraday, Nauder, Becker, Lewis C, Becker, Diane M
Published in BMC medical genomics (07.06.2010)
Published in BMC medical genomics (07.06.2010)
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Genome-wide Linkage Analysis of Multiple Metabolic Factors: Evidence of Genetic Heterogeneity
Cheng, Ching‐Yu, Lee, Kristine E., Duggal, Priya, Moore, Emily L., Wilson, Alexander F., Klein, Ronald, Bailey‐Wilson, Joan E., Klein, Barbara E.K.
Published in Obesity (Silver Spring, Md.) (01.01.2010)
Published in Obesity (Silver Spring, Md.) (01.01.2010)
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Pleiotropy Analysis of Quantitative Traits at Gene Level by Multivariate Functional Linear Models
Wang, Yifan, Liu, Aiyi, Mills, James L., Boehnke, Michael, Wilson, Alexander F., Bailey-Wilson, Joan E., Xiong, Momiao, Wu, Colin O., Fan, Ruzong
Published in Genetic epidemiology (01.05.2015)
Published in Genetic epidemiology (01.05.2015)
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The 677C→T variant of MTHFR is the major genetic modifier of biomarkers of folate status in a young, healthy Irish population
Shane, Barry, Pangilinan, Faith, Mills, James L, Fan, Ruzong, Gong, Tingting, Cropp, Cheryl D, Kim, Yoonhee, Ueland, Per M, Bailey-Wilson, Joan E, Wilson, Alexander F, Brody, Lawrence C, Molloy, Anne M
Published in The American journal of clinical nutrition (01.12.2018)
Published in The American journal of clinical nutrition (01.12.2018)
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Gene‐level association analysis of ordinal traits with functional ordinal logistic regressions
Chiu, Chi‐Yang, Wang, Shuqi, Zhang, Bingsong, Luo, Yutong, Simpson, Claire, Zhang, Wei, Wilson, Alexander F., Bailey‐Wilson, Joan E., Agron, Elvira, Chew, Emily Y., Zhang, Jun, Xiong, Momiao, Fan, Ruzong
Published in Genetic epidemiology (01.07.2022)
Published in Genetic epidemiology (01.07.2022)
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