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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 5 (of 5 Records)

Query Trace: Disease and SCN11A[original query]
Genetic Variants Underlying Risk of Intracranial Aneurysms: Insights from a GWAS in Portugal.
PloS one 2015 10 (7): e0133422.
Abrantes Patrícia, Santos Maria M, Sousa Inês, Xavier Joana M, Francisco Vânia, Krug Tiago, Sobral João, Matos Mafalda, Martins Madalena, Jacinto António, Coiteiro Domingos, Oliveira Sofia
Na channel variants in patients with painful and nonpainful peripheral neuropathy.
Neurology. Genetics 2017 Dec 3 (6): e207.
Wadhawan Samir, Pant Saumya, Golhar Ryan, Kirov Stefan, Thompson John, Jacobsen Leslie, Qureshi Irfan, Ajroud-Driss Senda, Freeman Roy, Simpson David M, Smith A Gordon, Hoke Ahmet, Bristow Linda
Homozygosity for the SCN10A Polymorphism rs6795970 Is Associated With Hypoalgesic Inflammatory Bowel Disease Phenotype.
Frontiers in medicine 2018 12 5 324.
Gonzalez-Lopez Eugene, Imamura Kawasawa Yuka, Walter Vonn, Zhang Lijun, Koltun Walter A, Huang Xuemei, Vrana Kent E, Coates Matthew
The Importance of Multiple Gene Analysis for Diagnosis and Differential Diagnosis in Charcot Marie Tooth Disease.
Turkish neurosurgery 2021 6 31 (6): 888-895.
Yalcintepe Sinem, Gurkan Hakan, Dogan Ipek Gungor, Demir Selma, Sag Sebnem Ozemri, Kabayegit Zehra Manav, Atli Emine Ikbal, Atli Engin, Eker Damla, Temel Sehime Guls
Standing genetic variation affects phenotypic heterogeneity in an SCN5A-mutation founder population with excess sudden cardiac death.
Heart rhythm 2023 2 .
Isaacs Aaron, Barysenka Andrei, Ter Bekke Rachel M A, Helderman-van den Enden Apollonia T J M, van den Wijngaard Arthur, Volders Paul G A, Stoll Moni
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