Thomas Eggermann

发表

Genetic variation in the schizophrenia-risk gene neuregulin1 correlates with differences in frontal brain activation in a working memory task in healthy individuals

Nadim Joni Shah, Tilo Kircher, Axel Krug, 2008, NeuroImage.

UPDtool: a tool for detection of iso- and heterodisomy in parent-child trios using SNP microarrays

Marc Sturm, Christopher M. Schroeder, Thomas Eggermann, 2013, Bioinform..

Effect of CACNA1C rs1006737 on neural correlates of verbal fluency in healthy individuals

Tilo Kircher, Axel Krug, Vanessa Nieratschker, 2010, NeuroImage.

A putative high risk diplotype of the G72 gene is in healthy individuals associated with better performance in working memory functions and altered brain activity in the medial temporal lobe

Nadim Joni Shah, Tilo Kircher, Axel Krug, 2009, NeuroImage.

CHAPTER 5 – Genetics: Basic Concepts and Testing

Carsten Bergmann, Thomas Eggermann, T. Eggermann, 2008 .

MAOA-VNTR polymorphism modulates context-dependent dopamine release and aggressive behavior in males

Paul Cumming, Felix M. Mottaghy, Ingo Vernaleken, 2016, NeuroImage.

COMT genotype and its role on hippocampal–prefrontal regions in declarative memory

Tilo Kircher, Axel Krug, N Jon Shah, 2010, NeuroImage.

The effect of Neuregulin 1 on neural correlates of episodic memory encoding and retrieval

Tilo Kircher, Axel Krug, Markus M. Nöthen, 2010, NeuroImage.

Genetic variation in schizophrenia-risk-gene dysbindin 1 modulates brain activation in anterior cingulate cortex and right temporal gyrus during language production in healthy individuals

Nadim Joni Shah, Tilo Kircher, Axel Krug, 2009, NeuroImage.

Genetic variation in the schizophrenia-risk gene neuregulin1 correlates with personality traits in healthy individuals

Tilo Kircher, Axel Krug, Marcella Rietschel, 2008, European Psychiatry.

Impact of schizophrenia‐risk gene dysbindin 1 on brain activation in bilateral middle frontal gyrus during a working memory task in healthy individuals

Tilo Kircher, Axel Krug, Marcella Rietschel, 2009, Human brain mapping.

Genetic counseling in Robertsonian translocations der(13;14): Frequencies of reproductive outcomes and infertility in 101 pedigrees

Thomas Eggermann, Hartmut Engels, A. Latos-Bieleńska, 2008, American journal of medical genetics. Part A.

Kaiso mediates human ICR1 methylation maintenance and H19 transcriptional fine regulation

Thomas Eggermann, Jerry Pelletier, R. Cencic, 2016, Clinical Epigenetics.

A rapid microarray based whole genome analysis for detection of uniparental disomy

Murat Bastepe, Thomas Eggermann, Andreas Dufke, 2005, Human mutation.

The effect of the COMT val158met polymorphism on neural correlates of semantic verbal fluency

Tilo Kircher, Axel Krug, N. Jon Shah, 2009, European Archives of Psychiatry and Clinical Neuroscience.

Genetic variation in the schizophrenia‐risk gene neuregulin 1 correlates with brain activation and impaired speech production in a verbal fluency task in healthy individuals

Nadim Jon Shah, Tilo Kircher, Axel Krug, 2009, Human brain mapping.

Clinical significance of copy number variations in the 11p15.5 imprinting control regions: new cases and review of the literature

Thomas Eggermann, Andreas Dufke, Michael Bonin, 2012, Journal of Medical Genetics.

Spectrum of mutations in the gene for autosomal recessive polycystic kidney disease (ARPKD/PKHD1).

Carsten Bergmann, Sabine Rudnik-Schöneborn, Klaus Zerres, 2003, Journal of the American Society of Nephrology : JASN.

The impact of dystrobrevin‐binding protein 1 (DTNBP1) on neural correlates of episodic memory encoding and retrieval

Nadim Jon Shah, Tilo Kircher, Axel Krug, 2009, Human brain mapping.

PKHD1 mutations in families requesting prenatal diagnosis for autosomal recessive polycystic kidney disease (ARPKD)

Carsten Bergmann, Sabine Rudnik-Schöneborn, Klaus Zerres, 2004, Human mutation.

Neuropsychological Correlates of Transcription Factor AP-2Beta, and Its Interaction with COMT and MAOA in Healthy Females

Ingo Vernaleken, Gerhard Gründer, Klaus Zerres, 2013, Neuropsychobiology.