Publications:

Network expansion of genetic associations defines a pleiotropy map of human cell biology.

Nature Genetics

Barrio-Hernandez, Inigo I; Schwartzentruber, Jeremy J; Shrivastava, Anjali A; Del-Toro, Noemi N; Gonzalez, Asier A; Zhang, Qian Q; Mountjoy, Edward E; Suveges, Daniel D; Ochoa, David D; Ghoussaini, Maya M; Bradley, Glyn G; Hermjakob, Henning H; Orchard, Sandra S; Dunham, Ian I; Anderson, Carl A CA; Porras, Pablo P; Beltrao, Pedro P

Publication Date: 2023-02-23

Variant appearance in text: FBN1: 3299G>T; Gly1100Val

PubMed Link: 36823319

Variant Present in the following documents:

• 41588_2023_1327_MOESM4_ESM.xlsx, sheet 6

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Clinical characteristics and survival of children with hypertrophic cardiomyopathy in China: A multicentre retrospective cohort study.

Eclinicalmedicine

Chan, Wenxiu W; Yang, Shiwei S; Wang, Jian J; Tong, Shilu S; Lin, Minyin M; Lu, Pengtao P; Yao, Ruen R; Wu, Lanping L; Chen, Lijun L; Guo, Ying Y; Shen, Jie J; Liu, Tingliang T; Li, Fen F; Chen, Huiwen H; Zhang, Hao H; Wang, Shushui S; Fu, Lijun L

Publication Date: 2022-07

Variant appearance in text: FBN1: 3299G>T; Gly1100Val

PubMed Link: 35747179

Variant Present in the following documents:

• mmc1.pdf

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Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorder.

Genome Medicine

Normand, Elizabeth A EA; Braxton, Alicia A; Nassef, Salma S; Ward, Patricia A PA; Vetrini, Francesco F; He, Weimin W; Patel, Vipulkumar V; Qu, Chunjing C; Westerfield, Lauren E LE; Stover, Samantha S; Dharmadhikari, Avinash V AV; Muzny, Donna M DM; Gibbs, Richard A RA; Dai, Hongzheng H; Meng, Linyan L; Wang, Xia X; Xiao, Rui R; Liu, Pengfei P; Bi, Weimin W; Xia, Fan F; Walkiewicz, Magdalena M; Van den Veyver, Ignatia B IB; Eng, Christine M CM; Yang, Yaping Y

Publication Date: 2018-09-28

Variant appearance in text: FBN1: 3299G>T; G1100V

PubMed Link: 30266093

Variant Present in the following documents:

• Main text
• 13073_2018_Article_582.pdf

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Identification of the minimal combination of clinical features in probands for efficient mutation detection in the FBN1 gene.

European Journal Of Human Genetics : Ejhg

Stheneur, Chantal C; Collod-Béroud, Gwenaëlle G; Faivre, Laurence L; Buyck, Jean François JF; Gouya, Laurent L; Le Parc, Jean-Marie JM; Moura, Bertrand B; Muti, Christine C; Grandchamp, Bernard B; Sultan, Gilles G; Claustres, Mireille M; Aegerter, Philippe P; Chevallier, Bertrand B; Jondeau, Guillaume G; Boileau, Catherine C

Publication Date: 2009-09

Variant appearance in text: FBN1: 3299G>T

PubMed Link: 19293843

Variant Present in the following documents:

• Main text

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Clinical and mutation-type analysis from an international series of 198 probands with a pathogenic FBN1 exons 24-32 mutation.

European Journal Of Human Genetics : Ejhg

Faivre, L L; Collod-Beroud, G G; Callewaert, B B; Child, A A; Binquet, C C; Gautier, E E; Loeys, B L BL; Arbustini, E E; Mayer, K K; Arslan-Kirchner, M M; Stheneur, C C; Kiotsekoglou, A A; Comeglio, P P; Marziliano, N N; Wolf, J E JE; Bouchot, O O; Khau-Van-Kien, P P; Beroud, C C; Claustres, M M; Bonithon-Kopp, C C; Robinson, P N PN; Adès, L L; De Backer, J J; Coucke, P P; Francke, U U; De Paepe, A A; Jondeau, G G; Boileau, C C

Publication Date: 2009-04

Variant appearance in text: FBN1: 3299G>T; Gly1100Val

PubMed Link: 19002209

Variant Present in the following documents:

• Main text

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