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)
Get full text
Journal Article
A genome-wide association study identifies a susceptibility locus for biliary atresia on 2p16.1 within the gene EFEMP1
Chen, Ying, Gilbert, Melissa A, Grochowski, Christopher M, McEldrew, Deborah, Llewellyn, Jessica, Waisbourd-Zinman, Orith, Hakonarson, Hakon, Bailey-Wilson, Joan E, Russo, Pierre, Wells, Rebecca G, Loomes, Kathleen M, Spinner, Nancy B, Devoto, Marcella
Published in PLoS genetics (13.08.2018)
Published in PLoS genetics (13.08.2018)
Get full text
Journal Article
A rare FGF5 candidate variant (rs112475347) for predisposition to nonsquamous, nonsmall‐cell lung cancer
Cannon‐Albright, Lisa A., Teerlink, Craig C., Stevens, Jeff, Facelli, Julio C., Carr, Shamus R., Allen‐Brady, Kristina, Puri, Sonam, Bailey‐Wilson, Joan E., Musolf, Anthony M., Akerley, Wallace
Published in International journal of cancer (15.07.2023)
Published in International journal of cancer (15.07.2023)
Get full text
Journal Article
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)
Get full text
Journal Article
Increased Burden of Rare Sequence Variants in GnRH-Associated Genes in Women With Hypothalamic Amenorrhea
Delaney, Angela, Burkholder, Adam B, Lavender, Christopher A, Plummer, Lacey, Mericq, Veronica, Merino, Paulina M, Quinton, Richard, Lewis, Katie L, Meader, Brooke N, Albano, Alessandro, Shaw, Natalie D, Welt, Corrine K, Martin, Kathryn A, Seminara, Stephanie B, Biesecker, Leslie G, Bailey-Wilson, Joan E, Hall, Janet E
Published in The journal of clinical endocrinology and metabolism (08.03.2021)
Published in The journal of clinical endocrinology and metabolism (08.03.2021)
Get full text
Journal Article
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)
Get full text
Journal Article
Assessing the Genetic Predisposition of Education on Myopia: A Mendelian Randomization Study
Cuellar-Partida, Gabriel, Lu, Yi, Kho, Pik Fang, Hewitt, Alex W., Wichmann, H.-Erich, Yazar, Seyhan, Stambolian, Dwight, Bailey-Wilson, Joan E., Wojciechowski, Robert, Wang, Jie Jin, Mitchell, Paul, Mackey, David A., MacGregor, Stuart
Published in Genetic epidemiology (01.01.2016)
Published in Genetic epidemiology (01.01.2016)
Get full text
Journal Article
Gene‐based analysis of bi‐variate survival traits via functional regressions with applications to eye diseases
Zhang, Bingsong, Chiu, Chi‐Yang, Yuan, Fang, Sang, Tian, Cook, Richard J, Wilson, Alexander F., Bailey‐Wilson, Joan E., Chew, Emily Y., Xiong, Momiao, Fan, Ruzong
Published in Genetic epidemiology (01.07.2021)
Published in Genetic epidemiology (01.07.2021)
Get full text
Journal Article
High incidence of unrecognized visceral/neurological late-onset Niemann-Pick disease, type C1, predicted by analysis of massively parallel sequencing data sets
Wassif, Christopher A., Cross, Joanna L., Iben, James, Sanchez-Pulido, Luis, Cougnoux, Antony, Platt, Frances M., Ory, Daniel S., Ponting, Chris P., Bailey-Wilson, Joan E., Biesecker, Leslie G., Porter, Forbes D.
Published in Genetics in medicine (01.01.2016)
Published in Genetics in medicine (01.01.2016)
Get full text
Journal Article
A Recurrent Mutation in PARK2 Is Associated with Familial Lung Cancer
Xiong, Donghai, Wang, Yian, Kupert, Elena, Simpson, Claire, Pinney, Susan M., Gaba, Colette R., Mandal, Diptasri, Schwartz, Ann G., Yang, Ping, de Andrade, Mariza, Pikielny, Claudio, Byun, Jinyoung, Li, Yafang, Stambolian, Dwight, Spitz, Margaret R., Liu, Yanhong, Amos, Christopher I., Bailey-Wilson, Joan E., Anderson, Marshall, You, Ming
Published in American journal of human genetics (05.02.2015)
Published in American journal of human genetics (05.02.2015)
Get full text
Journal Article
Functional Linear Models for Association Analysis of Quantitative Traits
Fan, Ruzong, Wang, Yifan, Mills, James L., Wilson, Alexander F., Bailey-Wilson, Joan E., Xiong, Momiao
Published in Genetic epidemiology (01.11.2013)
Published in Genetic epidemiology (01.11.2013)
Get full text
Journal Article
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)
Get full text
Journal Article
ComPaSS‐GWAS: A method to reduce type I error in genome‐wide association studies when replication data are not available
Sabourin, Jeremy A., Cropp, Cheryl D., Sung, Heejong, Brody, Lawrence C., Bailey‐Wilson, Joan E., Wilson, Alexander F.
Published in Genetic epidemiology (01.02.2019)
Published in Genetic epidemiology (01.02.2019)
Get full text
Journal Article
EPHA2 is associated with age-related cortical cataract in mice and humans
Jun, Gyungah, Guo, Hong, Klein, Barbara E K, Klein, Ronald, Wang, Jie Jin, Mitchell, Paul, Miao, Hui, Lee, Kristine E, Joshi, Tripti, Buck, Matthias, Chugha, Preeti, Bardenstein, David, Klein, Alison P, Bailey-Wilson, Joan E, Gong, Xiaohua, Spector, Tim D, Andrew, Toby, Hammond, Christopher J, Elston, Robert C, Iyengar, Sudha K, Wang, Bingcheng
Published in PLoS genetics (01.07.2009)
Published in PLoS genetics (01.07.2009)
Get full text
Journal Article
Gene‐based association analysis of survival traits via functional regression‐based mixed effect cox models for related samples
Chiu, Chi‐yang, Zhang, Bingsong, Wang, Shuqi, Shao, Jingyi, Lakhal‐Chaieb, M'Hamed Lajmi, Cook, Richard J., Wilson, Alexander F., Bailey‐Wilson, Joan E., Xiong, Momiao, Fan, Ruzong
Published in Genetic epidemiology (01.12.2019)
Published in Genetic epidemiology (01.12.2019)
Get full text
Journal Article
A novel de novo TP63 mutation in whole‐exome sequencing of a Syrian family with Oral cleft and ectrodactyly
Simpson, Claire L., Kimble, Danielle C., Chandrasekharappa, Settara C., Alqosayer, Khalid, Holzinger, Emily, Carrington, Blake, McElderry, John, Sood, Raman, Al‐Souqi, Ghiath, Albacha‐Hejazi, Hasan, Bailey‐Wilson, Joan E.
Published in Molecular genetics & genomic medicine (01.08.2023)
Published in Molecular genetics & genomic medicine (01.08.2023)
Get full text
Journal Article
Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy
Afshari, Natalie A, Igo, Jr, Robert P, Morris, Nathan J, Stambolian, Dwight, Sharma, Shiwani, Pulagam, V Lakshmi, Dunn, Steven, Stamler, John F, Truitt, Barbara J, Rimmler, Jacqueline, Kuot, Abraham, Croasdale, Christopher R, Qin, Xuejun, Burdon, Kathryn P, Riazuddin, S Amer, Mills, Richard, Klebe, Sonja, Minear, Mollie A, Zhao, Jiagang, Balajonda, Elmer, Rosenwasser, George O, Baratz, Keith H, Mootha, V Vinod, Patel, Sanjay V, Gregory, Simon G, Bailey-Wilson, Joan E, Price, Marianne O, Price, Jr, Francis W, Craig, Jamie E, Fingert, John H, Gottsch, John D, Aldave, Anthony J, Klintworth, Gordon K, Lass, Jonathan H, Li, Yi-Ju, Iyengar, Sudha K
Published in Nature communications (30.03.2017)
Published in Nature communications (30.03.2017)
Get full text
Journal Article
Inferring disease risk genes from sequencing data in multiplex pedigrees through sharing of rare variants
Bureau, Alexandre, Begum, Ferdouse, Taub, Margaret A., Hetmanski, Jacqueline B., Parker, Margaret M., Albacha‐Hejazi, Hasan, Scott, Alan F., Murray, Jeffrey C., Marazita, Mary L., Bailey‐Wilson, Joan E., Beaty, Terri H., Ruczinski, Ingo
Published in Genetic epidemiology (01.02.2019)
Published in Genetic epidemiology (01.02.2019)
Get full text
Journal Article