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Annals of Human Genetics|September 22, 2026
Exome Sequencing Identifies Novel Variants Causing Hearing Loss in Three Consanguineous Pakistani Families: Insights From Genomics and Bioinformatics AnalysesZafar Ali, Najeeb Ullah, Muneeba Bibi, et al.Annals of Human Genetics|March 1, 1997
A two-locus model for hereditary non-polyposis colorectal cancer in Modena, ItalyC Scapoli, A Collins, P Benatti, et al.Annals of Human Genetics|March 1, 1997
Heterogeneous effects of natural selection on the Italian newbornsL A Zonta, P Astolfi, L UlizziAnnals of Human Genetics|March 1, 1997
The comparative role of consanguinity in infant and childhood mortality in PakistanJ C Grant, A H BittlesAnnals of Human Genetics|March 1, 1997
On extending the transmission/disequilibrium test (TDT)S R WilsonAnnals of Human Genetics|January 1, 1989
Cytosolic aldehyde dehydrogenase (ALDH1) variants found in alcohol flushersA Yoshida, V Davé, R J Ward, et al.Annals of Human Genetics|November 14, 2014
The association between the polymorphisms in a sodium channel gene SCN7A and essential hypertension: a case-control study in the Northern Han ChineseBei Zhang, Mei Li, Lijuan Wang, et al.Annals of Human Genetics|November 14, 2014
Autosomal dominant hearing loss resulting from p.R75Q mutation in the GJB2 gene: nonsyndromic presentation in a South Indian familyAmritkumar Pavithra, Mathiyalagan Selvakumari, Venkatesan Nityaa, et al.Annals of Human Genetics|February 3, 2016
Differentially Methylated Genomic Regions in Birth-Weight Discordant Twin PairsMubo Chen, Jan Baumbach, Fabio Vandin, et al.Annals of Human Genetics|February 3, 2016
On Sample Size and Power Calculation for Variant Set-Based Association TestsBaolin Wu, James S PankowPageof 231