A homozygous FANCM mutation underlies a familial case of non-syndromic primary ovarian insufficiency

Individuals with FANCM biallelic mutations do not develop Fanconi anemia, but show risk for breast cancer, chemotherapy toxicity and may display chromosome fragility

(2017) Irene Catucci et al.   GENETICS IN MEDICINE

Biallelic truncating FANCM mutations cause early-onset cancer but not Fanconi anemia

(2017) Massimo Bogliolo et al.   GENETICS IN MEDICINE

Human foetal ovary shares meiotic preventing factors with the developing testis

(2017) Nelly Frydman et al.   HUMAN REPRODUCTION

Association Between Loss-of-Function Mutations Within the FANCM Gene and Early-Onset Familial Breast Cancer

(2017) Guido Neidhardt et al.   JAMA Oncology

A novel action of follicle-stimulating hormone in the ovary promotes estradiol production without inducing excessive follicular growth before puberty

(2017) Charlotte M. François et al.   Scientific Reports

A non-senseMCM9mutation in a familial case of primary ovarian insufficiency

(2016) F. Fauchereau et al.   CLINICAL GENETICS

Interplay between Fanconi anemia and homologous recombination pathways in genome integrity

(2016) Johanna Michl et al.   EMBO JOURNAL

Premature Ovarian Insufficiency: New Perspectives on Genetic Cause and Phenotypic Spectrum

(2016) Elena J. Tucker et al.   ENDOCRINE REVIEWS

FANCMc.5101C>T mutation associates with breast cancer survival and treatment outcome

(2016) Johanna I. Kiiski et al.   INTERNATIONAL JOURNAL OF CANCER

The Fanconi anaemia pathway: new players and new functions

(2016) Raphael Ceccaldi et al.   NATURE REVIEWS MOLECULAR CELL BIOLOGY

FANCD2 functions as a critical factor downstream of MiTF to maintain the proliferation and survival of melanoma cells

(2016) Julie Bourseguin et al.   Scientific Reports

BRCA Mutations, DNA Repair Deficiency, and Ovarian Aging1

(2015) Kutluk Oktay et al.   BIOLOGY OF REPRODUCTION

Fanconi anemia: a model disease for studies on human genetics and advanced therapeutics

(2015) Massimo Bogliolo et al.   CURRENT OPINION IN GENETICS & DEVELOPMENT

Whole exome sequencing reveals concomitant mutations of multiple FA genes in individual Fanconi anemia patients

(2014) Lixian Chang et al.   BMC Medical Genomics

Exome sequencing identifies FANCM as a susceptibility gene for triple-negative breast cancer

(2014) Johanna I. Kiiski et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Hypersensitivity of Primordial Germ Cells to Compromised Replication-Associated DNA Repair Involves ATM-p53-p21 Signaling

(2014) Yunhai Luo et al.   PLoS Genetics

Cellular and Molecular Effect of MEHP Involving LXRα in Human Fetal Testis and Ovary

(2012) Vincent Muczynski et al.   PLoS One

The Fission Yeast FANCM Ortholog Directs Non-Crossover Recombination During Meiosis

(2012) A. Lorenz et al.   SCIENCE

FANCM Limits Meiotic Crossovers

(2012) W. Crismani et al.   SCIENCE

Impaired FANCD2 monoubiquitination and hypersensitivity to camptothecin uniquely characterize Fanconi anemia complementation group M

(2009) T. R. Singh et al.   BLOOD

Fancm-deficient mice reveal unique features of Fanconi anemia complementation group M

(2009) Sietske T. Bakker et al.   HUMAN MOLECULAR GENETICS

Association of BRCA1 Mutations With Occult Primary Ovarian Insufficiency: A Possible Explanation for the Link Between Infertility and Breast/Ovarian Cancer Risks

(2009) Kutluk Oktay et al.   JOURNAL OF CLINICAL ONCOLOGY