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Annals of Human Genetics|January 16, 2016
Preeclampsia is Associated with Decreased Methylation of the GNA12 PromoterWeiping Ye, Lu Shen, Ying Xiong, et al.Annals of Human Genetics|January 13, 2016
On Efficient and Accurate Calculation of Significance P-Values for Sequence Kernel Association Testing of Variant SetBaolin Wu, Weihua Guan, James S PankowAnnals of Human Genetics|July 10, 2015
Association of TCF7L2 Polymorphism with Diabetic Nephropathy in the South Indian PopulationDhanasekaran Bodhini, Manickam Chidambaram, Samuel Liju, et al.Annals of Human Genetics|February 1, 1981
Natural selection associated with birth weight. I. Selection intensity and selective deaths from birth to one month of lifeL Terrenato, M F Gravina, L UlizziAnnals of Human Genetics|October 14, 2025
Genetic Landscape of Pediatric Dyslipidemia in a Turkish Cohort: Insights From a Single-Center ExperienceKadri Murat Erdoğan, Mehmet Berkay Akcan, Havva Yazıcı, et al.Annals of Human Genetics|September 29, 2025
Identification and Functional Verification of Variants Associated With Clubfoot and Arthrogrypotic Hand Deformation in a Multigeneration Polish FamilyEwa Hordyjewska-Kowalczyk, Akshaya Ramanujam, Adrian Odrzywolski, et al.Annals of Human Genetics|June 28, 2016
De Novo Truncating Mutation of TRIM8 Causes Early-Onset Epileptic EncephalopathyYasunari Sakai, Ryoko Fukai, Yuki Matsushita, et al.Annals of Human Genetics|January 1, 1986
Phenotypic resemblance in birth weight between first cousinsM P Mi, M Earle, J KagawaAnnals of Human Genetics|January 1, 1986
Genetic polymorphism and fertility parameters in the Aymara of Chile and BoliviaR Chakraborty, R E Ferrell, S A Barton, et al.Annals of Human Genetics|June 10, 2021
An identical-by-descent novel splice-donor variant in PRUNE1 causes a neurodevelopmental syndrome with prominent dystonia in two consanguineous Sudanese familiesMahmoud Koko, Ashraf Yahia, Liena E Elsayed, et al.Pageof 231