Identifying Genetic Factors in Common Diseases: More Helpful in Relation to Etiology Than Prediction

Por Nöthen, Markus M, Propping, Peter
Publicado em 2013

New Genetic Findings in Schizophrenia: Is there Still Room for the Dopamine Hypothesis of Schizophrenia?

Por Nieratschker, Vanessa, Nöthen, Markus M., Rietschel, Marcella
Publicado em 2010

Systemic mast cell activation disease: the role of molecular genetic alterations in pathogenesis, heritability and diagnostics

Por Haenisch, Britta, Nöthen, Markus M, Molderings, Gerhard J
Publicado em 2012

New findings in the genetics of major psychoses

Por Nöthen, Markus M, Nieratschker, Vanessa, Cichon, Sven, Rietschel, Marcella
Publicado em 2010

MicroRNAs as the cause of schizophrenia in 22q11.2 deletion carriers, and possible implications for idiopathic disease: a mini-review

Por Forstner, Andreas J., Degenhardt, Franziska, Schratt, Gerhard, Nöthen, Markus M.
Publicado em 2013

Genetics of dyslexia: the evolving landscape

Por Schumacher, Johannes, Hoffmann, Per, Schmäl, Christine, Schulte‐Körne, Gerd, Nöthen, Markus M
Publicado em 2007

A systematic eQTL study of cis–trans epistasis in 210 HapMap individuals

Por Becker, Jessica, Wendland, Jens R, Haenisch, Britta, Nöthen, Markus M, Schumacher, Johannes
Publicado em 2012

Familial Occurrence of Systemic Mast Cell Activation Disease

Por Molderings, Gerhard J., Haenisch, Britta, Bogdanow, Manuela, Fimmers, Rolf, Nöthen, Markus M.
Publicado em 2013

Single Nucleotide Variation Analysis in 65 Candidate Genes for CNS Disorders in a Representative Sample of the European Population

Por Freudenberg-Hua, Yun, Freudenberg, Jan, Kluck, Nadine, Cichon, Sven, Propping, Peter, Nöthen, Markus M.
Publicado em 2003

Genes and Schizophrenia: The G72/G30 Gene Locus in Psychiatric Disorders: A Challenge to Diagnostic Boundaries?

Por Abou Jamra, Rami, Schmael, Christine, Cichon, Sven, Rietschel, Marcella, Schumacher, Johannes, Nöthen, Markus M.
Publicado em 2006

Using Network Methodology to Infer Population Substructure

Por Prokopenko, Dmitry, Hecker, Julian, Silverman, Edwin, Nöthen, Markus M., Schmid, Matthias, Lange, Christoph, Loehlein Fier, Heide
Publicado no PLoS One (2015)

Expression profiling and bioinformatic analyses suggest new target genes and pathways for human hair follicle related microRNAs

Por Hochfeld, Lara M., Anhalt, Thomas, Reinbold, Céline S., Herrera-Rivero, Marisol, Fricker, Nadine, Nöthen, Markus M., Heilmann-Heimbach, Stefanie
Publicado no BMC Dermatol (2017)

Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia

Por Hillmer, Axel M., Kruse, Roland, Betz, Regina C., Schumacher, Johannes, Heyn, Uwe, Propping, Peter, Nöthen, Markus M., Cichon, Sven
Publicado em 2001

A One-Degree-of-Freedom Test for Supra-Multiplicativity of SNP Effects

Por Herold, Christine, Ramirez, Alfredo, Drichel, Dmitriy, Lacour, André, Vaitsiakhovich, Tatsiana, Nöthen, Markus M., Jessen, Frank, Maier, Wolfgang, Becker, Tim
Publicado em 2013

Exploring genetic variants predisposing to diabetes mellitus and their association with indicators of socioeconomic status

Por Schmidt, Börge, Dragano, Nico, Scherag, André, Pechlivanis, Sonali, Hoffmann, Per, Nöthen, Markus M, Erbel, Raimund, Jöckel, Karl-Heinz, Moebus, Susanne
Publicado em 2014

The FU gene and its possible protein isoforms

Por Østerlund, Torben, Everman, David B, Betz, Regina C, Mosca, Monica, Nöthen, Markus M, Schwartz, Charles E, Zaphiropoulos, Peter G, Toftgård, Rune
Publicado em 2004

The Effect of Neurogranin on Neural Correlates of Episodic Memory Encoding and Retrieval

Por Krug, Axel, Krach, Sören, Jansen, Andreas, Nieratschker, Vanessa, Witt, Stephanie H., Shah, N. Jon, Nöthen, Markus M., Rietschel, Marcella, Kircher, Tilo
Publicado em 2013

Localization of a Gene for Syndactyly Type 1 to Chromosome 2q34-q36

Por Bosse, Kristin, Betz, Regina C., Lee, Young-Ae, Wienker, Thomas F., Reis, André, Kleen, Heidi, Propping, Peter, Cichon, Sven, Nöthen, Markus M.
Publicado em 2000

Effect of the G72 (DAOA) putative risk haplotype on cognitive functions in healthy subjects

Por Jansen, Andreas, Krach, Sören, Krug, Axel, Markov, Valentin, Eggermann, Thomas, Zerres, Klaus, Thimm, Markus, Nöthen, Markus M, Treutlein, Jens, Rietschel, Marcella, Kircher, Tilo
Publicado em 2009

Risk loci for coronary artery calcification replicated at 9p21 and 6q24 in the Heinz Nixdorf Recall Study

Por Pechlivanis, Sonali, Mühleisen, Thomas W, Möhlenkamp, Stefan, Schadendorf, Dirk, Erbel, Raimund, Jöckel, Karl-Heinz, Hoffmann, Per, Nöthen, Markus M, Scherag, André, Moebus, Susanne
Publicado em 2013