Publications:

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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: PIK3CA: 1066G>A; Val356Ile

PubMed Link: 36823319

Variant Present in the following documents:

• 41588_2023_1327_MOESM4_ESM.xlsx, sheet 6

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Analysis of single-nucleotide polymorphisms in genes associated with triple-negative breast cancer.

Frontiers In Genetics

G, Vigneshwaran V; Hasan, Qurratulain Annie QA; Kumar, Rahul R; Eranki, Avinash A

Publication Date: 2022

Variant appearance in text: PIK3CA: V356I

PubMed Link: 36561320

Variant Present in the following documents:

• Table3.xlsx, sheet 1
• Table2.xlsx, sheet 5

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Scalable multiplex co-fractionation/mass spectrometry platform for accelerated protein interactome discovery.

Nature Communications

Havugimana, Pierre C PC; Goel, Raghuveera Kumar RK; Phanse, Sadhna S; Youssef, Ahmed A; Padhorny, Dzmitry D; Kotelnikov, Sergei S; Kozakov, Dima D; Emili, Andrew A

Publication Date: 2022-07-13

Variant appearance in text: PIK3CA: 1066G>A; V356M

PubMed Link: 35831314

Variant Present in the following documents:

• 41467_2022_31809_MOESM8_ESM.xlsx, sheet 3

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Germline pathogenic variant in PIK3CA leading to symmetrical overgrowth with marked macrocephaly and mild global developmental delay.

Molecular Genetics & Genomic Medicine

Zollino, Marcella M; Ranieri, Carlotta C; Grossi, Valentina V; Leoni, Chiara C; Lattante, Serena S; Mazzà, Daniela D; Simone, Cristiano C; Resta, Nicoletta N

Publication Date: 2019-08

Variant appearance in text: PIK3CA: Val356Ile

PubMed Link: 31290289

Variant Present in the following documents:

• Main text
• MGG3-7-e845.pdf

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Finding driver mutations in cancer: Elucidating the role of background mutational processes.

Plos Computational Biology

Brown, Anna-Leigh AL; Li, Minghui M; Goncearenco, Alexander A; Panchenko, Anna R AR

Publication Date: 2019-04

Variant appearance in text: PIK3CA: V356I

PubMed Link: 31034466

Variant Present in the following documents:

• pcbi.1006981.s010.xlsx, sheet 1

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Assessing the clinical value of targeted massively parallel sequencing in a longitudinal, prospective population-based study of cancer patients.

British Journal Of Cancer

Wong, S Q SQ; Fellowes, A A; Doig, K K; Ellul, J J; Bosma, T J TJ; Irwin, D D; Vedururu, R R; Tan, A Y-C AY; Weiss, J J; Chan, K S KS; Lucas, M M; Thomas, D M DM; Dobrovic, A A; Parisot, J P JP; Fox, S B SB

Publication Date: 2015-04-14

Variant appearance in text: PIK3CA: 1066G>A; Val356Ile

PubMed Link: 25742471

Variant Present in the following documents:

• bjc201580x7.xls, sheet 1

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Survival analysis of infected mice reveals pathogenic variations in the genome of avian H1N1 viruses.

Scientific Reports

Koçer, Zeynep A ZA; Fan, Yiping Y; Huether, Robert R; Obenauer, John J; Webby, Richard J RJ; Zhang, Jinghui J; Webster, Robert G RG; Wu, Gang G

Publication Date: 2014-12-12

Variant appearance in text: PI3K: V356I

PubMed Link: 25503687

Variant Present in the following documents:

• srep07455-s1.pdf

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Germline PIK3CA and AKT1 mutations in Cowden and Cowden-like syndromes.

American Journal Of Human Genetics

Orloff, Mohammed S MS; He, Xin X; Peterson, Charissa C; Chen, Fusong F; Chen, Jin-Lian JL; Mester, Jessica L JL; Eng, Charis C

Publication Date: 2013-01-10

Variant appearance in text: PIK3CA: 1066G>A

PubMed Link: 23246288

Variant Present in the following documents:

• Main text

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