2002 - C.W. Cotterman Award, American Society of Human Genetics
Harald H.H. Göring mainly focuses on Genetics, Genetic linkage, Genome-wide association study, Allele and Gene. His research in Single-nucleotide polymorphism, Linkage disequilibrium, Locus, Haplotype and Mutation are components of Genetics. In his study, Candidate gene is strongly linked to Lupus erythematosus, which falls under the umbrella field of Single-nucleotide polymorphism.
His Genetic linkage research integrates issues from Errors-in-variables models, Statistics, Pedigree chart, Quantitative trait locus and Genetic association. Harald H.H. Göring has included themes like Hippocampal formation, Neuroscience, Neuroimaging and Brain size in his Genome-wide association study study. His Allele study integrates concerns from other disciplines, such as Lymphoblastoid cell, Intervertebral disk and Exon.
Harald H.H. Göring spends much of his time researching Genetics, Quantitative trait locus, Genetic linkage, Genome-wide association study and Gene. All of his Genetics and Single-nucleotide polymorphism, Locus, Allele, Candidate gene and Genetic association investigations are sub-components of the entire Genetics study. His work carried out in the field of Allele brings together such families of science as Intervertebral disk and Genotype.
His Quantitative trait locus research incorporates elements of Genetic variation and Allele frequency. His Genetic linkage research is multidisciplinary, incorporating elements of Pedigree chart, Internal medicine, Statistics, Heritability and Linkage. Harald H.H. Göring studied Genome-wide association study and Neuroscience that intersect with White matter.
His primary areas of study are Genetics, Gene, Internal medicine, Endocrinology and Pedigree chart. Genetics is represented through his Genome-wide association study and Locus research. His study looks at the relationship between Gene and topics such as Heritability, which overlap with Consanguinity, CpG site, Methylation and Proteomics.
The concepts of his Internal medicine study are interwoven with issues in Efflux and Type 2 diabetes. Harald H.H. Göring combines subjects such as Chromosome and Genetic correlation with his study of Endocrinology. His Pedigree chart research includes elements of Cohort study, Whole genome sequencing and Imputation, Genotyping, Haplotype.
Genetics, Genome-wide association study, Apolipoprotein B, Locus and Cholesterol are his primary areas of study. His research brings together the fields of Endophenotype and Genetics. His biological study spans a wide range of topics, including Hippocampal formation, Alzheimer's disease, Episodic memory and Spatial memory.
The various areas that Harald H.H. Göring examines in his Apolipoprotein B study include Efflux and Gene knockdown. He focuses mostly in the field of Locus, narrowing it down to topics relating to Allele and, in certain cases, Single-nucleotide polymorphism. His study looks at the relationship between Cholesterol and fields such as Structural variation, as well as how they intersect with chemical problems.
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Common genetic variants influence human subcortical brain structures.
Derrek P. Hibar;Jason L. Stein;Jason L. Stein;Miguel E. Renteria;Alejandro Arias-Vasquez.
Polymorphisms in the Tyrosine Kinase 2 and Interferon Regulatory Factor 5 Genes Are Associated with Systemic Lupus Erythematosus
Snaevar Sigurdsson;Gunnel Nordmark;Harald H.H. Göring;Katarina Lindroos.
American Journal of Human Genetics (2005)
Identification of common variants associated with human hippocampal and intracranial volumes
Jason L Stein;Sarah E Medland;Sarah E Medland;Alejandro Arias Vasquez;Alejandro Arias Vasquez;Derrek P Hibar.
Nature Genetics (2012)
Discovery of expression QTLs using large-scale transcriptional profiling in human lymphocytes.
Harald H H Göring;Joanne E Curran;Matthew P Johnson;Thomas D Dyer.
Nature Genetics (2007)
The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data
Paul M. Thompson;Jason L. Stein;Sarah E. Medland;Derrek P. Hibar.
Brain Imaging and Behavior (2014)
Large upward bias in estimation of locus-specific effects from genomewide scans
Harald H.H. Göring;Joseph D. Terwilliger;Joseph D. Terwilliger;John Blangero.
American Journal of Human Genetics (2001)
An Allele of COL9A2 Associated with Intervertebral Disc Disease
Susanna Annunen;Petteri Paassilta;Jaana Lohiniva;Merja Perälä.
The transcriptional landscape of age in human peripheral blood
Marjolein J. Peters;Roby Joehanes;Luke C. Pilling;Claudia Schurmann;Claudia Schurmann.
Nature Communications (2015)
Identification of a novel common genetic risk factor for lumbar disk disease.
Petteri Paassilta;Jaana Lohiniva;Harald H. H. Göring;Harald H. H. Göring;Merja Perälä.
Long-term neural and physiological phenotyping of a single human
Russell A. Poldrack;Russell A. Poldrack;Timothy O. Laumann;Oluwasanmi Koyejo;Brenda Gregory.
Nature Communications (2015)
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