Associated Papers
Novel variants associated with premature ovarian insufficiency in Russian adolescents.
Tsabai P et al.
Frontiers in Endocrinology, 2025
Activating mutations in CSF1R and additional receptor tyrosine kinases in histiocytic neoplasms.
Durham BH et al.
Nature Medicine, 2019
31768065 (PubMed )
Supplement: NIHMS1541330-supplement-1.pdf
Exome Sequencing in BRCA1- and BRCA2-Negative Greek Families Identifies MDM1 and NBEAL1 as Candidate Risk Genes for Hereditary Breast Cancer.
Glentis S et al.
Frontiers in Genetics, 2019
31681433 (PubMed )
Supplement: DataSheet_1.xlsx › Supplemetary_Table_10
Identification of Multiple Gene Mutations Accounts for a new Genetic Architecture of Primary Ovarian Insufficiency.
Bouilly J et al.
The Journal of Clinical Endocrinology and Metabolism, 2016
Alterations in the NF2/LATS1/LATS2/YAP Pathway in Schwannomas.
Oh JE et al.
Journal of Neuropathology and Experimental Neurology, 2015
TP53, MSH4, and LATS1 germline mutations in a family with clustering of nervous system tumors.
Kim YH et al.
The American Journal of Pathology, 2014
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