Publications:

Assessing variants of uncertain significance implicated in hearing loss using a comprehensive deafness proteome.

Human Genetics

Tollefson, Mallory R MR; Gogal, Rose A RA; Weaver, A Monique AM; Schaefer, Amanda M AM; Marini, Robert J RJ; Azaiez, Hela H; Kolbe, Diana L DL; Wang, Donghong D; Weaver, Amy E AE; Casavant, Thomas L TL; Braun, Terry A TA; Smith, Richard J H RJH; Schnieders, Michael J MJ

Publication Date: 2023-04-22

Variant appearance in text: COL4A5: 1913G>A; Gly638Asp

PubMed Link: 37086329

Variant Present in the following documents:

• 439_2023_2559_MOESM2_ESM.xlsx, sheet 1

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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: COL4A5: 1913G>A; Gly638Asp

PubMed Link: 36823319

Variant Present in the following documents:

• 41588_2023_1327_MOESM4_ESM.xlsx, sheet 6

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Improving mutation screening in familial hematuric nephropathies through next generation sequencing.

Journal Of The American Society Of Nephrology : Jasn

Morinière, Vincent V; Dahan, Karin K; Hilbert, Pascale P; Lison, Marieline M; Lebbah, Said S; Topa, Alexandra A; Bole-Feysot, Christine C; Pruvost, Solenn S; Nitschke, Patrick P; Plaisier, Emmanuelle E; Knebelmann, Bertrand B; Macher, Marie-Alice MA; Noel, Laure-Hélène LH; Gubler, Marie-Claire MC; Antignac, Corinne C; Heidet, Laurence L

Publication Date: 2014-12

Variant appearance in text: COL4A5: Gly638Asp

PubMed Link: 24854265

Variant Present in the following documents:

• Main text

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