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Molecular Genetics & Genomic Medicine|May 16, 2020
Novel mutation in USP26 associated with azoospermia in a Sertoli cell-only syndrome patientMaram Arafat, Atif Zeadna, Eliahu Levitas, et al.BMC Gastroenterology|March 2, 2002
A comparative study of gallstones from children and adults using FTIR spectroscopy and fluorescence microscopyOleg Kleiner, Jagannathan Ramesh, Mahmoud Huleihel, et al.Journal of Medical Genetics|May 25, 2017
Mutation in TDRD9 causes non-obstructive azoospermia in infertile menMaram Arafat, Iris Har-Vardi, Avi Harlev, et al.Biopolymers|March 3, 2004
Studies on acute human infections using FTIR microspectroscopy and cluster analysisJacov Mordehai, Jagannathan Ramesh, Mahmoud Huleihel, et al.Journal of the American Chemical Society|April 25, 2007
Sculpting the bicyclo[3.1.0]hexane template of carbocyclic nucleosides to improve recognition by herpes thymidine kinaseMaria J Comin, Riad Agbaria, Tsipi Ben-Kasus, et al.European Journal of Human Genetics : EJHG|August 20, 2021
Pathogenic variations in Germ Cell Nuclear Acidic Peptidase (GCNA) are associated with human male infertilityMaram Arafat, Sandra E Kleiman, Ali AbuMadighem, et al.Journal of Medical Genetics|June 13, 2020
Absence of SCAPER causes male infertility in humans and Drosophila by modulating microtubule dynamics during meiosisOhad Wormser, Ygal Levy, Anna Bakhrat, et al.Current Biology : CB|May 16, 2017
RPL10L Is Required for Male Meiotic Division by Compensating for RPL10 during Meiotic Sex Chromosome Inactivation in MiceLong Jiang, Tao Li, Xingxia Zhang, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 31, 2018
Correction: A homozygous FANCM frameshift pathogenic variant causes male infertilityHao Yin, Hui Ma, Sajjad Hussain, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 14, 2018
A homozygous FANCM frameshift pathogenic variant causes male infertilityHao Yin, Hui Ma, Sajjad Hussain, et al.Pageof 16