Britta Fiebig

PTHR1 Loss-of-Function Mutations in Familial, Nonsyndromic Primary Failure of Tooth Eruption

Eva L. Decker, Angelika Stellzig‐Eisenhauer, Britta Fiebig et al. · The American Journal of Human Genetics · 2008 · 179 citations · Full text

Dentistry, Oral Biology, Oral Diagnosis +10

Acetylcholine Receptor Pathway Mutations Explain Various Fetal Akinesia Deformation Sequence Disorders

Anne Michalk, Sigmar Stricker, Jutta Becker et al. · The American Journal of Human Genetics · 2008 · 142 citations · Full text

Life Sciences, Genetics, Neuroscience +10

Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2

Anna Marie Mulligan, Fergus J. Couch, Daniel Barrowdale et al. · Breast Cancer Research · 2011 · 118 citations · Full text

Medicine, Genetics, Oncology +17

Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers

Antonis C. Antoniou, Olga M. Sinilnikova, Lesley McGuffog et al. · Human Molecular Genetics · 2009 · 115 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2mutation carriers

Antonis C. Antoniou, Karoline Kuchenbaecker, Penny Soucy et al. · Breast Cancer Research · 2012 · 96 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17