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Institute of Human Genetics
Friedrich-Alexander-Universität Erlangen-Nürnberg
Medizinische Fakultät
Einrichtungen, die zum Universitätsklinikum Erlangen gehören
Overview
Publications
(729)
Research Grants
(48)
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Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study (2014)
Johnson N, Dudbridge F, Orr N, Gibson L, Jones ME, Schoemaker MJ, Folkerd EJ, et al.
Journal article
Polymorphisms in the RANK/RANKL genes and their effect on bone specific prognosis in breast cancer patients (2014)
Hein A, Bayer CM, Schrauder MG, Haeberle L, Heusinger K, Strick R, Ruebner M, et al.
Journal article
MicroRNA Related Polymorphisms and Breast Cancer Risk (2014)
Khan S, Greco D, Michailidou K, Milne RL, Muranen TA, Heikkinen T, Aaltonen K, et al.
Journal article
FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium (2014)
Agarwal D, Pineda S, Michailidou K, Herranz J, Pita G, Moreno LT, Alonso MR, et al.
Journal article
Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation (2014)
Ghoussaini M, Edwards SL, Michailidou K, Nord S, Lari RCS, Desai K, Kar S, et al.
Journal article
Genome-wide UPD screening in patients with intellectual disability (2014)
Schroeder C, Ekici AB, Moog U, Grasshoff U, Mau-Holzmann U, Sturm M, Vosseler V, et al.
Journal article
Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium (2014)
Milne RL, Burwinkel B, Michailidou K, Arias-Perez JI, Pilar Zamora M, Menendez-Rodriguez P, Hardisson D, et al.
Journal article
Clinical spectrum of females with HCCS mutation: from no clinical signs to a neonatal lethal form of the microphthalmia with linear skin defects (MLS) syndrome (2014)
Van Rahden VA, Rau I, Fuchs S, Kosyna FK, De Almeida HL, Fryssira H, Isidor B, et al.
Journal article
Duchenne muscular dystrophy and malignant hyperthermia: a genetic study of the ryanodine receptor in 47 patients (2014)
Rohde D, Schmitt H, Winterpacht A, Münster T
Journal article
A complex microcephaly syndrome in a Pakistani family associated with a novel missense mutation in RBBP8 and a heterozygous deletion in NRXN1 (2014)
Agha Z, Iqbal Z, Azam M, Siddique M, Willemsen MH, Kleefstra T, Zweier C, et al.
Journal article
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