Mirjam Larsen

Large scale multifactorial likelihood quantitative analysis of <i>BRCA1</i> and <i>BRCA2</i> variants: An ENIGMA resource to support clinical variant classification

Michael T. Parsons, Emma Tudini, Hongyan Li et al. · Human Mutation · 2019 · 152 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

Manuel A. R. Ferreira, Eric R. Gamazon, Fares Al‐Ejeh et al. · Nature Communications · 2019 · 138 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Diagnostic approach for FSHD revisited: SMCHD1 mutations cause FSHD2 and act as modifiers of disease severity in FSHD1

Mirjam Larsen, Simone Rost, Nady El Hajj et al. · European Journal of Human Genetics · 2014 · 109 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Germline loss-of-function variants in the BARD1 gene are associated with early-onset familial breast cancer but not ovarian cancer

Nana Weber‐Lassalle, Julika Borde, Konstantin Weber‐Lassalle et al. · Breast Cancer Research · 2019 · 64 citations · Full text

Life Sciences, Genetics, Oncology +17

Association of Genomic Domains in <i>BRCA1</i> and <i>BRCA2</i> with Prostate Cancer Risk and Aggressiveness

Vivek Patel, Evan L. Busch, Tara M. Friebel et al. · Cancer Research · 2019 · 52 citations · Full text

Medicine, Genetics, Oncology +17