Human Genome Epidemiology Literature Finder

---

Filtered By: Select to fine-tune your search Disease Gene Year Journal Country Study Design

Previous

Records 1 - 6 (of 6 Records)

Query Trace: Disease and PEX7[original query]
ASK1 and MAP2K6 as modifiers of age at onset in Huntington's disease. Journal of molecular medicine (Berlin, Germany) 2008 Apr 86 (4): 485-90. Arning Larissa, Monté Didier, Hansen Wiebke, Wieczorek Stefan, Jagiello Peter, Akkad Denis A, Andrich Jürgen, Kraus Peter H, Saft Carsten, Epplen Jörg Similar articles in PubMed
Association between peroxisomal biogenesis factor 7 and autism spectrum disorders in a Korean population. Journal of child neurology 2012 Oct 27 (10): 1270-5. Ro MyungJa, Park JungWon, Nam Min, Bang Hee Jung, Yang Jaewon, Choi Kyung-Sik, Kim Su Kang, Chung Joo-Ho, Kwack KyuB Similar articles in PubMed
Using whole-exome sequencing to identify inherited causes of autism. Neuron 2013 Jan 77 (2): 2. Yu TW, Chahrour MH, Coulter ME, Jiralerspong S, Okamura-Ikeda K, Ataman B, Schmitz-Abe K, Harmin DA, Adli M, Malik AN, D'Gama AM, Lim ET, Sanders SJ, Mochida GH, Partlow JN, Sunu CM, Felie JM, Rodriguez J, Nasir RH, Ware J, Joseph RM, Hill RS, Kwan BY, Al-Saffar M, Mukaddes NM, Hashmi A, Balkhy S, Gascon GG, Hisama FM, Leclair E, Poduri A, Oner O, Al-Saad S, Al-Awadi SA, Bastaki L, Ben-Omran T, Teebi AS, Al-Gazali L, Eapen V, Stevens CR, Rappaport L, Gabriel SB, Markianos K, State MW, Greenberg ME, Taniguchi H, Braverman NE, Morrow EM, Walsh CA Similar articles in PubMed
Comprehensive Exonic Sequencing of Known Ataxia Genes in Episodic Ataxia. Biomedicines 2020 5 8 (5): . Maksemous Neven, Sutherland Heidi G, Smith Robert A, Haupt Larisa M, Griffiths Lyn Similar articles in PubMed
A Pex7 Deficient Mouse Series Correlates Biochemical and Neurobehavioral Markers to Genotype Severity-Implications for the Disease Spectrum of Rhizomelic Chondrodysplasia Punctata Type 1. Frontiers in cell and developmental biology 2022 7 10 886316. Fallatah Wedad, Cui Wei, Di Pietro Erminia, Carter Grace T, Pounder Brittany, Dorninger Fabian, Pifl Christian, Moser Ann B, Berger Johannes, Braverman Nancy Similar articles in PubMed
Gene and pathway based burden analyses in familial lymphoid cancer cases: Rare variants in immune pathway genes. PloS one 2023 6 18 (6): e0287602. Sneha Ralli, Samantha J Jones, Stephen Leach, Henry T Lynch, Angela R Brooks-Wils Similar articles in PubMed