Securing the use of existing sample collections for future human genetic research

od Kanoungi, George, Nürnberg, Peter, Nothnagel, Michael
izdano v Eur J Hum Genet (2017)

HomozygosityMapper—an interactive approach to homozygosity mapping

od Seelow, Dominik, Schuelke, Markus, Hildebrandt, Friedhelm, Nürnberg, Peter
Izdano 2009

Next Generation Sequencing of miRNAs – Strategies, Resources and Methods

od Motameny, Susanne, Wolters, Stefanie, Nürnberg, Peter, Schumacher, Björn
Izdano 2010

Cerebral vasculopathy is a common feature in Aicardi–Goutières syndrome associated with SAMHD1 mutations

od du Moulin, Marcel, Nürnberg, Peter, Crow, Yanick J., Rutsch, Frank
Izdano 2011

Simple ClinVar: an interactive web server to explore and retrieve gene and disease variants aggregated in ClinVar database

od Pérez-Palma, Eduardo, Gramm, Marie, Nürnberg, Peter, May, Patrick, Lal, Dennis
izdano v Nucleic Acids Res (2019)

Paternal relatedness and age proximity regulate social relationships among adult female rhesus macaques

od Widdig, Anja, Nürnberg, Peter, Krawczak, Michael, Streich, Wolf Jürgen, Bercovitch, Fred B.
Izdano 2001

Late diagnosis of a truncating WISP3 mutation entails a severe phenotype of progressive pseudorheumatoid dysplasia

od Alawbathani, Salem, Kawalia, Amit, Karakaya, Mert, Altmüller, Janine, Nürnberg, Peter, Cirak, Sebahattin
izdano v Cold Spring Harb Mol Case Stud (2018)

Effect of neurofibromatosis type I mutations on a novel pathway for adenylyl cyclase activation requiring neurofibromin and Ras

od Hannan, Frances, Ho, Ivan, Tong, James Jiayuan, Zhu, Yinghua, Nurnberg, Peter, Zhong, Yi
Izdano 2006

A novel VPS13B mutation in two brothers with Cohen syndrome, cutis verticis gyrata and sensorineural deafness

od Mégarbané, André, Slim, Rima, Nürnberg, Gudrun, Ebermann, Inga, Nürnberg, Peter, Bolz, Hanno Jörn
Izdano 2009

A longitudinal analysis of reproductive skew in male rhesus macaques.

od Widdig, Anja, Bercovitch, Fred B., Streich, Wolf Jürgen, Sauermann, Ulrike, Nürnberg, Peter, Krawczak, Michael
Izdano 2004

Adequate use of allele frequencies in Hispanics—a problem elucidated in nephrotic syndrome

od Chernin, Gil, Heeringa, Saskia F., Vega-Warner, Virginia, Schoeb, Dominik S., Nürnberg, Peter, Hildebrandt, Friedhelm
Izdano 2009

Recurrent and Prolonged Infections in a Child with a Homozygous IFIH1 Nonsense Mutation

od Zaki, Maha, Thoenes, Michaela, Kawalia, Amit, Nürnberg, Peter, Kaiser, Rolf, Heller, Raoul, Bolz, Hanno J.
izdano v Front Genet (2017)

Effects of PPP1R1B (DARPP-32) Polymorphism on Feedback-Related Brain Potentials Across the Life Span

od Hämmerer, Dorothea, Biele, Gudio, Müller, Viktor, Thiele, Holger, Nürnberg, Peter, Heekeren, Hauke R., Li, Shu-Chen
Izdano 2013

Rare Mutations of CACNB2 Found in Autism Spectrum Disease-Affected Families Alter Calcium Channel Function

od Breitenkamp, Alexandra F. S., Matthes, Jan, Nass, Robert Daniel, Sinzig, Judith, Lehmkuhl, Gerd, Nürnberg, Peter, Herzig, Stefan
Izdano 2014

A translational approach to dystroglycanopathies: a frequent type of muscular dystrophy

od Cirak, Sebahattin, Wang, Haicui, Heredia, Raul, Muntoni, Francesco, Hathout, Yetrib, Herkenrath, Peter, Dötsch, Jörg, Nürnberg, Peter
izdano v Mol Cell Pediatr (2015)

Alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism are both ATP1A3-related disorders

od Rosewich, Hendrik, Thiele, Holger, Ohlenbusch, Andreas, Maschke, Ulrike, Frommolt, Peter, Nürnberg, Peter, Brockmann, Knut, Gärtner, Jutta
izdano v Mol Cell Pediatr (2014)

Tumor suppression in basal keratinocytes via dual non-cell-autonomous functions of a Na,K-ATPase beta subunit

od Hatzold, Julia, Beleggia, Filippo, Herzig, Hannah, Altmüller, Janine, Nürnberg, Peter, Bloch, Wilhelm, Wollnik, Bernd, Hammerschmidt, Matthias
izdano v eLife (2016)

Genes from Chagas Susceptibility Loci That Are Differentially Expressed in T. cruzi-Resistant Mice Are Candidates Accounting for Impaired Immunity

od Graefe, Sebastian E. B., Streichert, Thomas, Budde, Birgit S., Nürnberg, Peter, Steeg, Christiane, Müller-Myhsok, Bertram, Fleischer, Bernhard
Izdano 2006

Genome-wide Analysis Indicates More Asian than Melanesian Ancestry of Polynesians

od Kayser, Manfred, Lao, Oscar, Saar, Kathrin, Brauer, Silke, Wang, Xingyu, Nürnberg, Peter, Trent, Ronald J., Stoneking, Mark
Izdano 2008

Mutation of Solute Carrier SLC16A12 Associates with a Syndrome Combining Juvenile Cataract with Microcornea and Renal Glucosuria

od Kloeckener-Gruissem, Barbara, Vandekerckhove, Kristof, Nürnberg, Gudrun, Neidhardt, John, Zeitz, Christina, Nürnberg, Peter, Schipper, Isaak, Berger, Wolfgang
Izdano 2008