Common Breast Cancer-Predisposition Alleles Are Associated with Breast Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

Antonis C. Antoniou, Amanda B. Spurdle, Olga M. Sinilnikova, +81

The American Journal of Human Genetics

Allelic VariantBreast OncologyBreast Cancer RiskCancer RiskGenetics +6

Interplay between BRCA1 and RHAMM Regulates Epithelial Apicobasal Polarization and May Influence Risk of Breast Cancer

Christopher A. Maxwell, Javier Benítez, Laia Gómez‐Baldó, +51

PLoS Biology

Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for <i>BRCA1</i> and <i>BRCA2</i> Mutation Carriers: Implications for Risk Prediction

Antonis C. Antoniou, Jonathan Beesley, Lesley McGuffog, +170

Cancer Research

Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers

Antonis C. Antoniou, Christiana Kartsonaki, Olga M. Sinilnikova, +39

Human Molecular Genetics

GeneticsGenetic EpidemiologyCommon AllelesPathologyHuman Polymorphism +14

Sequence Variants in SLC6A3, DRD2, and BDNF Genes and Time to Levodopa-Induced Dyskinesias in Parkinson’s Disease

Natalie Kaplan, Aya Vituri, Amos D. Korczyn, +9

Journal of Molecular Neuroscience

Neurodegenerative DiseasesMolecular NeuroscienceSequence VariantsMedicineParkinson Disease +9

A role for<i>TENM1</i>mutations in congenital general anosmia

Anna Alkelai, Tsviya Olender, Rebecca Haffner‐Krausz, +12

Clinical Genetics

Neurobiological MechanismDevelopmental BiologyMolecular NeuroscienceMendelian DisorderSynapse Organization +13

Noncoding deletions reveal a gene that is critical for intestinal function

Danit Oz-Levi, Tsviya Olender, Ifat Bar-Joseph, +40

Nature

Systems BiologyIntestinal FunctionGeneticsGenomic MechanismGene Characterization +7

Germline mutations in BRIP1 and PALB2 in Jewish high cancer risk families

Irene Catucci, Roni Milgrom, Anya Kushnir, +8

Familial Cancer

Somatic VariantCancer EpidemiologyCancer RiskMedicineGenetics +7

The rate of the predominant Jewish mutations in the BRCA1, BRCA2, MSH2 and MSH6 genes in unselected Jewish endometrial cancer patients

Frida Barak, Roni Milgrom, Yael Laitman, +7

Gynecologic Oncology

Predominant Jewish MutationsOncologySomatic VariantMedicineMsh6 Genes +7

Next-generation sequencing of patients with congenital anosmia

Anna Alkelai, Tsviya Olender, Catherine Dodé, +12

European Journal of Human Genetics

Next-generation SequencingPediatricsCongenital AnosmiaMolecular DiagnosticsSequencing +1