Katalog der Deutschen Nationalbibliothek

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	31	Evolutionary conserved networks of human height identify multiple Mendelian causes of short stature Enthalten in European journal of human genetics 26.2.2019: 1-11
	32	Inflammation-induced glycolytic switch controls suppressivity of mesenchymal stem cells via STAT1 glycosylation Enthalten in Leukemia 24.1.2019: 1-14
	33	Loss of function of SVBP leads to autosomal recessive intellectual disability, microcephaly, ataxia, and hypotonia Enthalten in Genetics in medicine 4.1.2019: 1-7
	34	Addition of triple negativity of breast cancer as an indicator for germline mutations in predisposing genes increases sensitivity of clinical selection criteria Hoyer, Juliane. - Erlangen : Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 2018
	35	Integrative bioinformatics analysis characterizing the role of EDC3 in mRNA decay and its association to intellectual disability Scheller, Ute. - Erlangen : Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 2018
	36	Risk, Prediction and Prevention of Hereditary Breast Cancer – Large-Scale Genomic Studies in Times of Big and Smart Data Enthalten in Geburtshilfe und Frauenheilkunde Bd. 78, 2018, Nr. 05: 481-492
	37	The polynucleotide kinase 3′-phosphatase gene (PNKP) is involved in Charcot-Marie-Tooth disease (CMT2B2) previously related to MED25 Enthalten in Neurogenetics 24.7.2018: 1-11
	38	AMPA-receptor specific biogenesis complexes control synaptic transmission and intellectual ability Bréchet, Aline. - Freiburg : Universität, 2019
	39	Clinical validation of genetic variants associated with in vitro chemotherapy-related lymphoblastoid cell toxicity Fasching, Peter Andreas. - Frankfurt am Main : Universitätsbibliothek Johann Christian Senckenberg, 2017
	40	Genome-wide association and targeted analysis of copy number variants with psoriatic arthritis in German patients Uebe, Steffen. - Erlangen : Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 2017