Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Heart, Lung, Blood and Sleep Disorders

Last data update: Jun 10, 2023. (Total: 217811Documents)
   dataset        GWAS Only
Filtered By:

Previous    

Records 1 - 4 (of 4 Records)

Query Trace: Heart Disorder[original query]
Genetic variants in incident SUDEP cases from a community-based prospective cohort with epilepsy.
Journal of neurology, neurosurgery, and psychiatry 2019 11 91 (2): 126-131.
Ge Yan, Ding Ding, Zhu Guoxing, Kwan Patrick, Wang Wenzhi, Hong Zhen, Sander Josemir
Identification of a variant hotspot in MYBPC3 and of a novel CSRP3 autosomal recessive alteration in a cohort of Polish patients with hypertrophic cardiomyopathy.
Polish archives of internal medicine 2020 Jan .
Lipari Martina, Wypasek Ewa, Karpi?ski Marek, Tomkiewicz-Pajak Lidia, Laino Luigi, Binni Francesco, Giannarelli Diana, Rubi? Pawe?, Petkow-Dimitrow Pawe?, Undas Anetta, Grammatico Paola, Bottillo Ire
Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity. GWAS Catalog
Nature genetics 2021 Jan .
Harper Andrew R, Goel Anuj, Grace Christopher, Thomson Kate L, Petersen Steffen E, Xu Xiao, Waring Adam, Ormondroyd Elizabeth, Kramer Christopher M, Ho Carolyn Y, Neubauer Stefan, , Tadros Rafik, Ware James S, Bezzina Connie R, Farrall Martin, Watkins Hu
A novel likely pathogenic variant in the FBXO32 gene associated with dilated cardiomyopathy according to whole?exome sequencing.
BMC medical genomics 2022 11 15 (1): 234.
Ghasemi Serwa, Mahdavi Mohammad, Maleki Majid, Salahshourifar Iman, Kalayinia Sami
TOP