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Nature Communications|May 3, 2025
Rare genetic variation in PTPRB is associated with central serous chorioretinopathy, varicose veins and glaucomaJoel T Rämö, Bryan R Gorman, Lu-Chen Weng, et al.Science (New York, N.Y.)|November 24, 1999
Genome sequence of the radioresistant bacterium Deinococcus radiodurans R1O White, J A Eisen, J F Heidelberg, et al.Nature|April 8, 2021
Genome-wide enhancer maps link risk variants to disease genesJoseph Nasser, Drew T Bergman, Charles P Fulco, et al.Plos Genetics|April 18, 2013
Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controlsLi Liu, Aniko Sabo, Benjamin M Neale, et al.Gastroenterology|February 19, 2018
Clinical and Genomic Correlates of Neutrophil Reactive Oxygen Species Production in Pediatric Patients With Crohn's DiseaseLee A Denson, Ingrid Jurickova, Rebekah Karns, et al.Journal of Medical Internet Research|July 2, 2016
A Dietary Feedback System for the Delivery of Consistent Personalized Dietary Advice in the Web-Based Multicenter Food4Me StudyHannah Forster, Marianne C Walsh, Clare B O'Donovan, et al.Neuron|May 8, 2018
Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 FamiliesPadhraig Gormley, Mitja I Kurki, Marjo Eveliina Hiekkala, et al.Science (New York, N.Y.)|December 15, 2018
Genome-wide de novo risk score implicates promoter variation in autism spectrum disorderJoon-Yong An, Kevin Lin, Lingxue Zhu, et al.Nature Communications|October 18, 2018
Phenome-wide association studies across large population cohorts support drug target validationDorothée Diogo, Chao Tian, Christopher S Franklin, et al.Nature Neuroscience|November 27, 2019
Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock proteinSali M K Farhan, Daniel P Howrigan, Liam E Abbott, et al.Pageof 163