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Ancestry estimation and control of population stratification for sequence-based association studies.
Published in:
Nature Genetics, 2014, v. 46, n. 4, p. 409, doi. 10.1038/ng.2924
By:
- Wang, Chaolong;
- Zhan, Xiaowei;
- Bragg-Gresham, Jennifer;
- Kang, Hyun Min;
- Stambolian, Dwight;
- Chew, Emily Y;
- Branham, Kari E;
- Heckenlively, John;
- Fulton, Robert;
- Wilson, Richard K;
- Mardis, Elaine R;
- Lin, Xihong;
- Swaroop, Anand;
- Zöllner, Sebastian;
- Abecasis, Gonçalo R
Publication type:
Article
Identification of a rare coding variant in complement 3 associated with age-related macular degeneration.
Published in:
Nature Genetics, 2013, v. 45, n. 11, p. 1375, doi. 10.1038/ng.2758
By:
- Zhan, Xiaowei;
- Larson, David E;
- Wang, Chaolong;
- Koboldt, Daniel C;
- Sergeev, Yuri V;
- Fulton, Robert S;
- Fulton, Lucinda L;
- Fronick, Catrina C;
- Branham, Kari E;
- Bragg-Gresham, Jennifer;
- Jun, Goo;
- Hu, Youna;
- Kang, Hyun Min;
- Liu, Dajiang;
- Othman, Mohammad;
- Brooks, Matthew;
- Ratnapriya, Rinki;
- Boleda, Alexis;
- Grassmann, Felix;
- von Strachwitz, Claudia
Publication type:
Article
CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration.
Published in:
Nature Genetics, 2006, v. 38, n. 9, p. 1049, doi. 10.1038/ng1871
By:
- Mingyao Li;
- Atmaca-Sonmez, Pelin;
- Othman, Mohammad;
- Branham, Kari E. H.;
- Khanna, Ritu;
- Wade, Michael S.;
- Yun Li;
- Liming Liang;
- Zareparsi, Sepideh;
- Swaroop, Anand;
- Abecasis, Gonçalo R.
Publication type:
Article
Whole genome sequencing of 4,787 individuals identifies gene-based rare variants in age-related macular degeneration.
Published in:
Human Molecular Genetics, 2024, v. 33, n. 4, p. 374, doi. 10.1093/hmg/ddad189
By:
- Kwong, Alan;
- Zawistowski, Matthew;
- Fritsche, Lars G;
- Zhan, Xiaowei;
- Bragg-Gresham, Jennifer;
- Branham, Kari E;
- Advani, Jayshree;
- Othman, Mohammad;
- Ratnapriya, Rinki;
- Teslovich, Tanya M;
- Stambolian, Dwight;
- Chew, Emily Y;
- Abecasis, Gonçalo R;
- Swaroop, Anand
Publication type:
Article
Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration.
Published in:
Human Molecular Genetics, 2014, v. 23, n. 21, p. 5827, doi. 10.1093/hmg/ddu276
By:
- Ratnapriya, Rinki;
- Zhan, Xiaowei;
- Fariss, Robert N.;
- Branham, Kari E.;
- Zipprer, David;
- Chakarova, Christina F.;
- Sergeev, Yuri V.;
- Campos, Maria M.;
- Othman, Mohammad;
- Friedman, James S.;
- Maminishkis, Arvydas;
- Waseem, Naushin H.;
- Brooks, Matthew;
- Rajasimha, Harsha K.;
- Edwards, Albert O.;
- Lotery, Andrew;
- Klein, Barbara E.;
- Truitt, Barbara J.;
- Li, Bingshan;
- Schaumberg, Debra A.
Publication type:
Article
Next Generation Genetic Testing for Retinitis Pigmentosa.
Published in:
Human Mutation, 2013, v. 34, n. 8, p. 1181, doi. 10.1002/humu.22357
By:
- Neveling, Kornelia;
- Collin, Rob W.J.;
- Gilissen, Christian;
- Huet, Ramon A.C.;
- Visser, Linda;
- Kwint, Michael P.;
- Gijsen, Sabine J.;
- Zonneveld, Marijke N.;
- Wieskamp, Nienke;
- Ligt, Joep;
- Siemiatkowska, Anna M.;
- Hoefsloot, Lies H.;
- Buckley, Michael F.;
- Kellner, Ulrich;
- Branham, Kari E.;
- den Hollander, Anneke I.;
- Hoischen, Alexander;
- Hoyng, Carel;
- Klevering, B. Jeroen;
- Born, L. Ingeborgh
Publication type:
Article
Complement factor H genetic variant and age-related macular degeneration: effect size, modifiers and relationship to disease subtype.
Published in:
International Journal of Epidemiology, 2012, v. 41, n. 1, p. 250, doi. 10.1093/ije/dyr204
By:
- Sofat, Reecha;
- Casas, Juan P;
- Webster, Andrew R;
- Bird, Alan C;
- Mann, Samantha S;
- Yates, John RW;
- Moore, Anthony T;
- Sepp, Tiina;
- Cipriani, Valentina;
- Bunce, Catey;
- Khan, Jane C;
- Shahid, Humma;
- Swaroop, Anand;
- Abecasis, Gonçalo;
- Branham, Kari E H;
- Zareparsi, Sepideh;
- Bergen, Arthur A;
- Klaver, Caroline CW;
- Baas, Dominique C;
- Zhang, Kang
Publication type:
Article

Found: 7

Ancestry estimation and control of population stratification for sequence-based association studies.

Identification of a rare coding variant in complement 3 associated with age-related macular degeneration.

CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration.

Whole genome sequencing of 4,787 individuals identifies gene-based rare variants in age-related macular degeneration.

Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration.

Next Generation Genetic Testing for Retinitis Pigmentosa.

Complement factor H genetic variant and age-related macular degeneration: effect size, modifiers and relationship to disease subtype.