Publications:

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Machine learning based combination of multi-omics data for subgroup identification in non-small cell lung cancer.

Scientific Reports

Khadirnaikar, Seema S; Shukla, Sudhanshu S; Prasanna, S R M SRM

Publication Date: 2023-03-21

Variant appearance in text: rs6426327

PubMed Link: 36944673

Variant Present in the following documents:

• 41598_2023_31426_MOESM3_ESM.xlsx, sheet 3

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Identification of novel meQTLs strongly associated with rheumatoid arthritis by large-scale epigenome-wide analysis.

Febs Open Bio

Tang, Guoping G; Sun, Chen C; Lv, Hongchao H; Zhang, Mingming M; Jiang, Yongshuai Y; Xu, Jing J

Publication Date: 2022-12

Variant appearance in text: rs6426327

PubMed Link: 36342317

Variant Present in the following documents:

• Main text

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Feasibility and ethics of using data from the Scottish newborn blood spot archive for research.

Communications Medicine

Cunningham-Burley, Sarah S; McCartney, Daniel L DL; Campbell, Archie A; Flaig, Robin R; Orange, Clare E L CEL; Porteous, Carol C; Aitken, Mhairi M; Mulholland, Ciaran C; Davidson, Sara S; McCafferty, Selena M SM; Murphy, Lee L; Wrobel, Nicola N; McCafferty, Sarah S; Wallace, Karen K; StClair, David D; Kerr, Shona S; Hayward, Caroline C; McIntosh, Andrew M AM; Sudlow, Cathie C; Marioni, Riccardo E RE; Pell, Jill J; Miedzybrodzka, Zosia Z; Porteous, David J DJ

Publication Date: 2022

Variant appearance in text: rs6426327

PubMed Link: 36210800

Variant Present in the following documents:

• 43856_2022_189_MOESM1_ESM.pdf

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Genetic Factors Associated With Tardive Dyskinesia: From Pre-clinical Models to Clinical Studies.

Frontiers In Pharmacology

Tsermpini, Evangelia Eirini EE; Redenšek, Sara S; Dolžan, Vita V

Publication Date: 2021

Variant appearance in text: rs6426327

PubMed Link: 35140610

Variant Present in the following documents:

• Main text
• fphar-12-834129.pdf

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DNA methylation of chronic lymphocytic leukemia with differential response to chemotherapy.

Scientific Data

Yosifov, Deyan Yordanov DY; Bloehdorn, Johannes J; Döhner, Hartmut H; Lichter, Peter P; Stilgenbauer, Stephan S; Mertens, Daniel D

Publication Date: 2020-05-01

Variant appearance in text: rs6426327

PubMed Link: 32358561

Variant Present in the following documents:

• 41597_2020_Article_456.pdf

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Intraventricular meningiomas frequently harbor NF2 mutations but lack common genetic alterations in TRAF7, AKT1, SMO, KLF4, PIK3CA, and TERT.

Acta Neuropathologica Communications

Jungwirth, Gerhard G; Warta, Rolf R; Beynon, Christopher C; Sahm, Felix F; von Deimling, Andreas A; Unterberg, Andreas A; Herold-Mende, Christel C; Jungk, Christine C

Publication Date: 2019-08-30

Variant appearance in text: rs6426327

PubMed Link: 31470906

Variant Present in the following documents:

• 40478_2019_793_MOESM1_ESM.xlsx, sheet 2

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Admixture Mapping of Subclinical Atherosclerosis and Subsequent Clinical Events Among African Americans in 2 Large Cohort Studies.

Circulation. Cardiovascular Genetics

Shendre, Aditi A; Wiener, Howard H; Irvin, Marguerite R MR; Zhi, Degui D; Limdi, Nita A NA; Overton, Edgar T ET; Wassel, Christina L CL; Divers, Jasmin J; Rotter, Jerome I JI; Post, Wendy S WS; Shrestha, Sadeep S

Publication Date: 2017-04

Variant appearance in text: rs6426327

PubMed Link: 28408707

Variant Present in the following documents:

• Main text

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Biallelic truncating mutations in FMN2, encoding the actin-regulatory protein Formin 2, cause nonsyndromic autosomal-recessive intellectual disability.

American Journal Of Human Genetics

Law, Rosalind R; Dixon-Salazar, Tracy T; Jerber, Julie J; Cai, Na N; Abbasi, Ansar A AA; Zaki, Maha S MS; Mittal, Kirti K; Gabriel, Stacey B SB; Rafiq, Muhammad Arshad MA; Khan, Valeed V; Nguyen, Maria M; Ali, Ghazanfar G; Copeland, Brett B; Scott, Eric E; Vasli, Nasim N; Mikhailov, Anna A; Khan, Muhammad Nasim MN; Andrade, Danielle M DM; Ayaz, Muhammad M; Ansar, Muhammad M; Ayub, Muhammad M; Vincent, John B JB; Gleeson, Joseph G JG

Publication Date: 2014-12-04

Variant appearance in text: rs6426327

PubMed Link: 25480035

Variant Present in the following documents:

• Main text

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Association of the HSPG2 gene with neuroleptic-induced tardive dyskinesia.

Neuropsychopharmacology : Official Publication Of The American College Of Neuropsychopharmacology

Syu, Aoi A; Ishiguro, Hiroki H; Inada, Toshiya T; Horiuchi, Yasue Y; Tanaka, Syunsuke S; Ishikawa, Maya M; Arai, Makoto M; Itokawa, Masanari M; Niizato, Kazuhiro K; Iritani, Shuji S; Ozaki, Norio N; Takahashi, Makoto M; Kakita, Akiyoshi A; Takahashi, Hitoshi H; Nawa, Hiroyuki H; Keino-Masu, Kazuko K; Arikawa-Hirasawa, Eri E; Arinami, Tadao T

Publication Date: 2010-04

Variant appearance in text: rs6426327

PubMed Link: 20072119

Variant Present in the following documents:

• Main text

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