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Nature Genetics|April 28, 2015
Germline RECQL mutations are associated with breast cancer susceptibilityCezary Cybulski, Jian Carrot-Zhang, Wojciech Kluźniak, et al.Neuro-Oncology|January 25, 2024
Invasive growth of brain metastases is linked to CHI3L1 release from pSTAT3-positive astrocytesMatthew Dankner, Sarah M Maritan, Neibla Priego, et al.Cancer Research|August 1, 2022
Germline Missense Variants in CDC20 Result in Aberrant Mitotic Progression and Familial CancerOwen J Chen, Ester Castellsagué, Mohamed Moustafa-Kamal, et al.Nature Communications|February 4, 2018
Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patientsJean-Louis Guéant, Céline Chéry, Abderrahim Oussalah, et al.Nature Communications|January 6, 2018
APRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patientsJean-Louis Guéant, Céline Chéry, Abderrahim Oussalah, et al.Acta Neuropathologica|February 10, 2018
NHLRC2 variants identified in patients with fibrosis, neurodegeneration, and cerebral angiomatosis (FINCA): characterisation of a novel cerebropulmonary diseaseJohanna Uusimaa, Riitta Kaarteenaho, Teija Paakkola, et al.The Journal of Clinical Investigation|December 6, 2019
DGCR8 microprocessor defect characterizes familial multinodular goiter with schwannomatosisBarbara Rivera, Javad Nadaf, Somayyeh Fahiminiya, et al.Genome Medicine|December 4, 2021
A functionally impaired missense variant identified in French Canadian families implicates FANCI as a candidate ovarian cancer-predisposing geneCaitlin T Fierheller, Laure Guitton-Sert, Wejdan M Alenezi, et al.Science (New York, N.Y.)|May 14, 2016
Histone H3K36 mutations promote sarcomagenesis through altered histone methylation landscapeChao Lu, Siddhant U Jain, Dominik Hoelper, et al.Cancer Research|June 25, 2017
Functionally Null RAD51D Missense Mutation Associates Strongly with Ovarian CarcinomaBarbara Rivera, Massimo Di Iorio, Jessica Frankum, et al.Pageof 5