Gerard Tromp


Ontology type: schema:Person     


Person Info

NAME

Gerard

SURNAME

Tromp

Publications in SciGraph latest 50 shown

  • 2019-12 The X chromosome and sex-specific effects in infectious disease susceptibility in HUMAN GENOMICS
  • 2018-12 Appetitive and reactive aggression are differentially associated with the STin2 genetic variant in the serotonin transporter gene in SCIENTIFIC REPORTS
  • 2018-05 Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity in NATURE GENETICS
  • 2018-05 Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity in NATURE GENETICS
  • 2018-01 Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity in NATURE GENETICS
  • 2017-12 Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals in BIODATA MINING
  • 2017-12 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function in SCIENTIFIC REPORTS
  • 2017-12 Corrigendum: Persisting positron emission tomography lesion activity and Mycobacterium tuberculosis mRNA after tuberculosis cure in NATURE MEDICINE
  • 2017-04 Corrigendum: Persisting positron emission tomography lesion activity and Mycobacterium tuberculosis mRNA after tuberculosis cure in NATURE MEDICINE
  • 2017-02-01 Rare and low-frequency coding variants alter human adult height in NATURE
  • 2017-02 Identifying gene–gene interactions that are highly associated with four quantitative lipid traits across multiple cohorts in HUMAN GENETICS
  • 2016-12 The complete genome sequence of the African buffalo (Syncerus caffer) in BMC GENOMICS
  • 2016-10 Persisting positron emission tomography lesion activity and Mycobacterium tuberculosis mRNA after tuberculosis cure in NATURE MEDICINE
  • 2016-08 eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants in BMC MEDICAL GENOMICS
  • 2016-06 A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough in THE PHARMACOGENOMICS JOURNAL
  • 2015-12 Prospective participant selection and ranking to maximize actionable pharmacogenetic variants and discovery in the eMERGE Network in GENOME MEDICINE
  • 2015-11 A Robust e-Epidemiology Tool in Phenotyping Heart Failure with Differentiation for Preserved and Reduced Ejection Fraction: the Electronic Medical Records and Genomics (eMERGE) Network in JOURNAL OF CARDIOVASCULAR TRANSLATIONAL RESEARCH
  • 2015-09 SMAD3 deficiency promotes vessel wall remodeling, collagen fiber reorganization and leukocyte infiltration in an inflammatory abdominal aortic aneurysm mouse model in SCIENTIFIC REPORTS
  • 2014-12 Population risk factor estimates for abdominal aortic aneurysm from electronic medical records: a case control study in BMC CARDIOVASCULAR DISORDERS
  • 2014-03 An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge in GENOME BIOLOGY
  • 2013-10 The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future in GENETICS IN MEDICINE
  • 2012-12 MicroRNA expression signature in human abdominal aortic aneurysms in BMC MEDICAL GENOMICS
  • 2012-05 Presence of Borrelia burgdorferi sensu lato antibodies in the serum of patients with abdominal aortic aneurysms in EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES
  • 2012 The Molecular Biology and Genetics of Aneurysms in MOLECULAR AND TRANSLATIONAL VASCULAR MEDICINE
  • 2011-12 Analysis of positional candidate genes in the AAA1 susceptibility locus for abdominal aortic aneurysms on chromosome 19 in BMC MEDICAL GENETICS
  • 2011-12 Regional expression of HOXA4 along the aorta and its potential role in human abdominal aortic aneurysms in BMC PHYSIOLOGY
  • 2010-08 Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm in NATURE GENETICS
  • 2010-07 Novel Genetic Mechanisms for Aortic Aneurysms in CURRENT ATHEROSCLEROSIS REPORTS
  • 2008-12 Analytical approaches to detect maternal/fetal genotype incompatibilities that increase risk of pre-eclampsia in BMC MEDICAL GENETICS
  • 2008-08 Haplotypes of Tumor Necrosis Factor Gene and Tracheal Aspirate Fluid Levels of Tumor Necrosis Factor-&agr; in Preterm Infants in PEDIATRIC RESEARCH
  • 2008-02 The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm in NATURE GENETICS
  • 2007-12 Whole genome expression profiling reveals a significant role for immune function in human abdominal aortic aneurysms in BMC GENOMICS
  • 2006-12 Identification of novel functional sequence variants in the gene for peptidase inhibitor 3 in BMC MEDICAL GENETICS
  • 2006-12 Evidence for association between the HLA-DQA locus and abdominal aortic aneurysms in the Belgian population: a case control study in BMC MEDICAL GENETICS
  • 2006-05 Community-Based, Nonprofit Organization-Sponsored Ultrasonography Screening Program for Abdominal Aortic Aneurysms Is Effective at Identifying Occult Aneurysms in ANNALS OF VASCULAR SURGERY
  • 2004-07 Elevated Expression of Matrix Metalloproteinase-13 in Abdominal Aortic Aneurysms in ANNALS OF VASCULAR SURGERY
  • 2004-06 Evidence of linkage and association on chromosome 20 for late-onset Alzheimer disease in NEUROGENETICS
  • 2004-05 Fine mapping of the Schnyder’s crystalline corneal dystrophy locus in HUMAN GENETICS
  • 2002-12 High-resolution physical map for chromosome 16q12.1-q13, the Blau syndrome locus in BMC GENOMICS
  • 2002-12 Search for intracranial aneurysm susceptibility gene(s) using Finnish families in BMC MEDICAL GENETICS
  • 1998-11 Fibulin-2 exhibits high degree of variability, but no structural changes concordant with abdominal aortic aneurysms in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 1998-03 First-stage autosomal genome screen in extended pedigrees suggests genes predisposing to low bone mineral density on chromosomes 1p, 2p and 4q in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 1995-09 Ehlers-Danlos Syndrome Type IV: A Single Base Substitution of the Last Nucleotide of Exon 34 in COL3A1 Leads to Exon Skipping in JOURNAL OF INVESTIGATIVE DERMATOLOGY
  • 1993-04 Deletion of 19 base pairs in intron 13 of the gene for the proα2(I) chain of type-I procollagen (COL1A2) causes exon skipping in a proband with type-I osteogenesis imperfecta in HUMAN GENETICS
  • 1991-12 Exclusion of COL1A1, COL1A2, and COL3A1 genes as candidate genes for Ehlers-Danlos syndrome type I in one large family in HUMAN GENETICS
  • 1986-03 Assessment of small polymorphisms in defined human collagen gene segments in HUMAN GENETICS
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