Fine-mapping of candidate region in Amish and Ashkenazi families confirms linkage of refractive error to a QTL on 1p34-p36

por Wojciechowski, Robert, Bailey-Wilson, Joan E., Stambolian, Dwight
Publicado 2009

MATCHCLIP: locate precise breakpoints for copy number variation using CIGAR string by matching soft clipped reads

por Wu, Yinghua, Tian, Lifeng, Pirastu, Mario, Stambolian, Dwight, Li, Hongzhe
Publicado 2013

Dissecting the genetic heterogeneity of myopia susceptibility in an Ashkenazi Jewish population using ordered subset analysis

por Simpson, Claire L., Wojciechowski, Robert, Ibay, Grace, Stambolian, Dwight, Bailey-Wilson, Joan E.
Publicado 2011

Age-related macular degeneration-associated variants at chromosome 10q26 do not significantly alter ARMS2 and HTRA1 transcript levels in the human retina

por Kanda, Atsuhiro, Stambolian, Dwight, Chen, Wei, Curcio, Christine A., Abecasis, Gonçalo R., Swaroop, Anand
Publicado 2010

Annotation and analysis of 10,000 expressed sequence tags from developing mouse eye and adult retina

por Yu, Jindan, Farjo, Rafal, MacNee, Sean P, Baehr, Wolfgang, Stambolian, Dwight E, Swaroop, Anand
Publicado 2003

Regional replication of association with refractive error on 15q14 and 15q25 in the Age-Related Eye Disease Study cohort

por Simpson, Claire L., Wojciechowski, Robert, Yee, Stephanie S., Soni, Poorva, Bailey-Wilson, Joan E., Stambolian, Dwight
Publicado 2013

Identification of three novel NHS mutations in families with Nance-Horan syndrome

por Huang, Kristen M., Wu, Junhua, Brooks, Simon P., Hardcastle, Alison J., Lewis, Richard Alan, Stambolian, Dwight
Publicado 2007

Copy number variants encompassing Mendelian disease genes in a large multigenerational family segregating bipolar disorder

por Kember, Rachel L, Georgi, Benjamin, Bailey-Wilson, Joan E, Stambolian, Dwight, Paul, Steven M, Bućan, Maja
Publicado 2015

Sequence and Expression of Complement Factor H Gene Cluster Variants and Their Roles in Age-Related Macular Degeneration Risk

por Hughes, Anne E., Bridgett, Stephen, Meng, Weihua, Li, Mingyao, Curcio, Christine A., Stambolian, Dwight, Bradley, Declan T.
Publicado 2016

Association of OCT-Derived Drusen Measurements with AMD-Associated Genotypic SNPs in the Amish Population

por Chavali, Venkata Ramana Murthy, Diniz, Bruno, Huang, Jiayan, Ying, Gui-Shuang, Sadda, SriniVas R., Stambolian, Dwight
Publicado 2015

Imaging Lenticular Autofluorescence in Older Subjects

por Charng, Jason, Tan, Rose, Luu, Chi D., Sadigh, Sam, Stambolian, Dwight, Guymer, Robyn H., Jacobson, Samuel G., Cideciyan, Artur V.
Publicado 2017

Deep learning enables accurate clustering with batch effect removal in single-cell RNA-seq analysis

por Li, Xiangjie, Wang, Kui, Lyu, Yafei, Pan, Huize, Zhang, Jingxiao, Stambolian, Dwight, Susztak, Katalin, Reilly, Muredach P., Hu, Gang, Li, Mingyao
Publicado 2020

Longitudinal evaluation of the distribution of intraretinal hyper-reflective foci in eyes with intermediate age-related macular degeneration

por Sadda, Srinivas, Verma, Aditya, Corradetti, Giulia, Nittala, Muneeswar, He, Ye, Nassisi, Marco, Velaga, Swetha Bindu, Haines, Jonathan, Pericak-Vance, Margaret, Stambolian, Dwight
Publicado 2023

Risk Factors for Progression of Age-Related Macular Degeneration: Population-Based Amish Eye Study

por Nittala, Muneeswar G., Corvi, Federico, Maram, Jyotsna, Velaga, Swetha B., Haines, Jonathan, Pericak-Vance, Margaret A., Stambolian, Dwight, Sadda, SriniVas R.
Publicado 2022

r2VIM: A new variable selection method for random forests in genome-wide association studies

por Szymczak, Silke, Holzinger, Emily, Dasgupta, Abhijit, Malley, James D., Molloy, Anne M., Mills, James L., Brody, Lawrence C., Stambolian, Dwight, Bailey-Wilson, Joan E.
Publicado 2016

Genomewide Association Study of Retinal Traits in the Amish Reveals Loci Influencing Drusen Development and Link to Age-Related Macular Degeneration

por Osterman, Michael D., Song, Yeunjoo E., Nittala, Muneeswar, Sadda, SriniVas R., Scott, William K., Stambolian, Dwight, Pericak-Vance, Margaret A., Haines, Jonathan L.
Publicado 2022

Caucasian Families Exhibit Significant Linkage of Myopia to Chromosome 11p

por Musolf, Anthony M., Simpson, Claire L., Moiz, Bilal A., Long, Kyle A., Portas, Laura, Murgia, Federico, Ciner, Elise B., Stambolian, Dwight, Bailey-Wilson, Joan E.
Publicado 2017

Relationship between the distribution of intra-retinal hyper-reflective foci and the progression of intermediate age-related macular degeneration

por Verma, Aditya, Corradetti, Giulia, He, Ye, Nittala, Muneeswar G., Nassisi, Marco, Velaga, Swetha B., Haines, Jonathan L., Pericak-Vance, Margaret A., Stambolian, Dwight, Sadda, SriniVas R.
Publicado 2023

Candidate high myopia loci on chromosomes 18p and 12q do not play a major role in susceptibility to common myopia

por Ibay, Grace, Doan, Betty, Reider, Lauren, Dana, Debra, Schlifka, Melissa, Hu, Heping, Holmes, Taura, O'Neill, Jennifer, Owens, Robert, Ciner, Elise, Bailey–Wilson, Joan E, Stambolian, Dwight
Publicado 2004

Myopia in Chinese families shows linkage to 10q26.13

por Musolf, Anthony M., Simpson, Claire L., Long, Kyle A., Moiz, Bilal A., Lewis, Deyana D., Middlebrooks, Candace D., Portas, Laura, Murgia, Federico, Ciner, Elise B., Bailey-Wilson, Joan E., Stambolian, Dwight
Publicado 2018