Associated Papers
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40009381 (PubMed )
Supplement: jamanetwopen-e2461639-s002.pdf
Toward clinical exomes in diagnostics and management of male infertility.
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American Journal of Human Genetics, 2024
Spectrum and Frequency of Germline FANCM Protein-Truncating Variants in 44,803 European Female Breast Cancer Cases.
Figlioli G et al.
Cancers, 2023
Spectrum of Germline Mutations Within Fanconi Anemia-Associated Genes Across Populations of Varying Ancestry.
Chan SH et al.
Jnci Cancer Spectrum, 2021
Novel Bi-Allelic Variants of FANCM Cause Sertoli Cell-Only Syndrome and Non-Obstructive Azoospermia.
Zhang Y et al.
Frontiers in Genetics, 2021
The Spectrum of FANCM Protein Truncating Variants in European Breast Cancer Cases.
Figlioli G et al.
Cancers, 2020
Bi-allelic Recessive Loss-of-Function Variants in FANCM Cause Non-obstructive Azoospermia.
Kasak L et al.
American Journal of Human Genetics, 2018
FANCM and RECQL genetic variants and breast cancer susceptibility: relevance to South Poland and West Ukraine.
Nguyen-Dumont T et al.
Bmc Medical Genetics, 2018
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