Publications:

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Analysis of CACNA1C and KCNH2 Risk Variants on Cardiac Autonomic Function in Patients with Schizophrenia.

Genes

Refisch, Alexander A; Komatsuzaki, Shoko S; Ungelenk, Martin M; Schumann, Andy A; Chung, Ha-Yeun HY; Schilling, Susann S SS; Jantzen, Wibke W; Schröder, Sabine S; Nöthen, Markus M MM; Mühleisen, Thomas W TW; Hübner, Christian A CA; Bär, Karl-Jürgen KJ

Publication Date: 2022-11-16

Variant appearance in text: rs1036145

PubMed Link: 36421807

Variant Present in the following documents:

• Main text
• genes-13-02132.pdf

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Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal

Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL

Publication Date: 2019-04

Variant appearance in text: rs1036145

PubMed Link: 30214008

Variant Present in the following documents:

• NIHMS1503453-supplement-3.xlsx, sheet 1

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Gene variants as risk factors for gastroschisis.

American Journal Of Medical Genetics. Part A

Padula, Amy M AM; Yang, Wei W; Schultz, Kathleen K; Tom, Lauren L; Lin, Bin B; Carmichael, Suzan L SL; Lammer, Edward J EJ; Shaw, Gary M GM

Publication Date: 2016-11

Variant appearance in text: rs1036145

PubMed Link: 27616475

Variant Present in the following documents:

• Main text
• AJMG-170-2788.pdf

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Association between polymorphisms in NOS3 and KCNH2 and social memory.

Frontiers In Neuroscience

Henningsson, Susanne S; Zettergren, Anna A; Hovey, Daniel D; Jonsson, Lina L; Svärd, Joakim J; Cortes, Diana S DS; Melke, Jonas J; Ebner, Natalie C NC; Laukka, Petri P; Fischer, Håkan H; Westberg, Lars L

Publication Date: 2015

Variant appearance in text: rs1036145

PubMed Link: 26539080

Variant Present in the following documents:

• Main text
• fnins-09-00393.pdf

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Personalized medicine in psychiatry: problems and promises.

Bmc Medicine

Ozomaro, Uzoezi U; Wahlestedt, Claes C; Nemeroff, Charles B CB

Publication Date: 2013-05-16

Variant appearance in text: rs1036145

PubMed Link: 23680237

Variant Present in the following documents:

• Main text
• 1741-7015-11-132.pdf

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Prevalence of arrhythmia-associated gene mutations and risk of sudden cardiac death in the Finnish population.

Annals Of Medicine

Lahtinen, Annukka M AM; Havulinna, Aki S AS; Noseworthy, Peter A PA; Jula, Antti A; Karhunen, Pekka J PJ; Perola, Markus M; Newton-Cheh, Christopher C; Salomaa, Veikko V; Kontula, Kimmo K

Publication Date: 2013-06

Variant appearance in text: rs1036145

PubMed Link: 23651034

Variant Present in the following documents:

• Main text

View BVdb publication page

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