Weller, J. I., Gershoni, M., & Ezra, E. (2021)., Genetic and environmental analysis of female calf survival in the Israel Holstein cattle population. Journal of Dairy Science

Foreman M, Gershoni M, Barkan D. (2020)., A Simplified and Efficient Method for Himar-1 Transposon Sequencing in Bacteria, Demonstrated by Creation and Analysis of a Saturated Transposon-Mutant Library in Mycobacterium abscessus. mSystems. 

Arafat, M., Harlev, A., Har-Vardi, I., Levitas, E., Priel, T., Gershoni, M., Searby, C., Sheffield, V. C., Lunenfeld, E., & Parvari, R. Mutation in CATIP (C2orf62) causes oligoteratoasthenozoospermia by affecting actin dynamics. Journal of medical genetics, 2020

Gershoni, M., Ezra, E., & Weller, J. I. Genetic and genomic analysis of long insemination interval in Israeli dairy cattle as an indicator of early abortions. Journal of Dairy Science, 2020.‏

Seroussi E, Shirak A, Gershoni M, Ezra E, de Abreu Santos DJ, Ma L, Liu GE. Bos taurus-indicus hybridization correlates with intralocus sexual-conflict effects of PRDM9 on male and female fertility in Holstein cattle. BMC Genet. 2019 

Gershoni M, Hauser R., Barda S., Lehavi O., Arama E., Pietrokovski S., & Kleiman S. E. A new MEIOB mutation is a recurrent cause for azoospermia and testicular meiotic arrest. Human Reproduction. 2019.

Nuta GC, Gilad Y, Gershoni M, Sznajderman A, Schlesinger T, Bialik S, Eisenstein M, Pietrokovski S, Kimchi A. A cancer associated somatic mutation in LC3B attenuates its binding to E1-like ATG7 protein and subsequent lipidation. Autophagy. 2019

Gershoni M, Hauser R, Yogev L, Lehavi O, Azem F, Yavetz H, Pietrokovski S, Kleiman SE. A familial study of azoospermic men identifies three novel causative mutations in three new human azoospermia genes. Genet Med. 2017 

Gershoni M*, Pietrokovski S. The landscape of sex-differential transcriptome and its consequent selection in human adults. BMC Biol. 2017 

Rappaport N, Twik M, Plaschkes I, Nudel R, Iny Stein T, Levitt J, Gershoni M, Morrey CP, Safran M, Lancet D. MalaCards: an amalgamated human disease compendium with diverse clinical and genetic annotation and structured search. Nucleic Acids Res. 2017  

Riemersma M, Mandel H, van Beusekom E, Gazzoli I, Roscioli T, Eran A, Gershoni-Baruch R, Gershoni M, Pietrokovski S, Vissers LE, Lefeber DJ, Willemsen MA, Wevers RA, van Bokhoven H. Absence of α- and β dystroglycan is associated with Walker-Warburg syndrome. Neurology. 2015 

Gershoni M, Levin L, Ovadia O, Toiw Y, Shani N, Dadon S, Barzilai N, Bergman A, Atzmon G, Wainstein J, Tsur A, Nijtmans L, Glaser B, Mishmar D. Disrupting mitochondrial-nuclear coevolution affects OXPHOS complex I integrity and impacts human health. Genome Biol Evol. 2014 

Gershoni M, Pietrokovski S. Reduced selection and accumulation of deleterious mutations in genes exclusively expressed in men. Nat Commun. 2014 

Gershoni M, Fuchs A, Shani N, Fridman Y, Corral-Debrinski M, Aharoni A, Frishman D, Mishmar D. Coevolution predicts direct interactions between mtDNA-encoded and nDNA-encoded subunits of oxidative phosphorylation complex I. J Mol Biol. 2010

Gershoni M, Templeton AR, Mishmar D. Mitochondrial bioenergetics as a major motive force of speciation. Bioessays. 2009 

Mishmar D, Gershoni M. Treating speciation processes as complex traits. Nature Reviews Genetics 8, 320 2007).

*Corresponding authors