Institute of Human Genetics


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Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

Publication year

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Abstract

Journal

Genetic predisposition to in situ and invasive lobular carcinoma of the breast (2014) Sawyer E, Roylance R, Petridis C, Brook MN, Nowinski S, Papouli E, Fletcher O, et al. Journal article Identification of new genetic susceptibility Loci for breast cancer through consideration of gene-environment interactions (2014) Schoeps A, Rudolph A, Seibold P, Dunning AM, Milne RL, Bojesen SE, Swerdlow A, et al. Journal article Human-induced pluripotent stem cells pave the road for a better understanding of motor neuron disease (2014) Winner B, Marchetto MC, Winkler J, Gage FH Journal article Gene dosage-dependent rescue of HSP neurite defects in SPG4 patients' neurons (2014) Havlicek S, Kohl Z, Mishra HK, Prots I, Eberhardt E, Denguir N, Wend H, et al. Journal article, Original article Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer (2014) Purrington KS, Slager S, Eccles D, Yannoukakos D, Fasching PA, Miron P, Carpenter J, et al. Journal article Accumulation of oligomer-prone ?-synuclein exacerbates synaptic and neuronal degeneration in vivo (2014) Rockenstein E, Nuber S, Overk CR, Ubhi K, Mante M, Patrick C, Adame A, et al. Journal article HER2 and TOP2A amplification in a hospital-based cohort of breast cancer patients: associations with patient and tumor characteristics (2014) Fasching PA, Weihbrecht S, Haeberle L, Gasparyan A, Villalobos IE, Ma Y, Ekici AB, et al. Journal article A large-scale assessment of two-way SNP interactions in breast cancer susceptibility using 46 450 cases and 42 461 controls from the breast cancer association consortium (2014) Milne RL, Herranz J, Michailidou K, Dennis J, Tyrer JP, Zamora MP, Arias-Perez JI, et al. Journal article Mutations affecting the SAND domain of DEAF1 cause intellectual disability with severe speech impairment and behavioral problems (2014) Vulto-Van Silfhout AT, Rajamanickam S, Jensik PJ, Vergult S, De Rocker N, Newhall KJ, Raghavan R, et al. Journal article HIBCH deficiency in a patient with phenotypic characteristics of mitochondrial disorders (2014) Reuter M, Sass JO, Leis T, Koehler J, Mayr JA, Feichtinger RG, Rauh M, et al. Journal article