Philip Jansen

About Philip Jansen

Philip Jansen, With an exceptional h-index of 26 and a recent h-index of 26 (since 2020), a distinguished researcher at Vrije Universiteit Amsterdam, specializes in the field of Epidemiology, complex trait genetics, clinical genetics, neuroimaging, polygenic risk scores.

His recent articles reflect a diverse array of research interests and contributions to the field:

Genome-Wide Analyses of Vocabulary Size in Infancy and Toddlerhood: Associations With Attention-Deficit/Hyperactivity Disorder, Literacy, and Cognition-Related Traits

Evaluation of 100 Dutch cases with 16p11. 2 deletion and duplication syndromes; from clinical manifestations towards personalized treatment options

Clinical and functional heterogeneity associated with the disruption of retinoic acid receptor beta

Obesity and the brain: structural and functional imaging studies, and opportunities for large-scale imaging genetics

Correspondence on “Frequency of truncating FLCN variants and Birt-Hogg-Dubé-associated phenotypes in a health care system population” by Savatt et al

A second update on mapping the human genetic architecture of COVID-19

Genetic Burden of TNNI3K in Diagnostic Testing of Patients With Dilated Cardiomyopathy and Supraventricular Arrhythmias

Genomic contributions to infant and toddler vocabulary scores: Implications for association with health-, cognition-, and behaviour-related outcomes

Philip Jansen Information

University

Position

MD PhD | Complex Trait Genetics | Clinical Genetics Amsterdam UMC

Citations(all)

7262

Citations(since 2020)

6789

Cited By

2786

hIndex(all)

26

hIndex(since 2020)

26

i10Index(all)

41

i10Index(since 2020)

39

Email

University Profile Page

Google Scholar

Philip Jansen Skills & Research Interests

Epidemiology

complex trait genetics

clinical genetics

neuroimaging

polygenic risk scores

Top articles of Philip Jansen

Genome-Wide Analyses of Vocabulary Size in Infancy and Toddlerhood: Associations With Attention-Deficit/Hyperactivity Disorder, Literacy, and Cognition-Related Traits

Biological psychiatry

2024/5/1

Evaluation of 100 Dutch cases with 16p11. 2 deletion and duplication syndromes; from clinical manifestations towards personalized treatment options

European Journal of Human Genetics

2024/4/11

Clinical and functional heterogeneity associated with the disruption of retinoic acid receptor beta

Genetics in Medicine

2023/8/1

Obesity and the brain: structural and functional imaging studies, and opportunities for large-scale imaging genetics

2023/1/1

Philip Jansen
Philip Jansen

H-Index: 18

Correspondence on “Frequency of truncating FLCN variants and Birt-Hogg-Dubé-associated phenotypes in a health care system population” by Savatt et al

Genetics in Medicine

2023/1/1

Genetic Burden of TNNI3K in Diagnostic Testing of Patients With Dilated Cardiomyopathy and Supraventricular Arrhythmias

Circulation: Genomic and Precision Medicine

2023/8

Genomic contributions to infant and toddler vocabulary scores: Implications for association with health-, cognition-, and behaviour-related outcomes

BioRxiv

2022/6/1

Polygenic risk for ADHD and ASD and their relation with cognitive measures in school children

Psychological medicine

2022/5

Exploring the genetic overlap between twelve psychiatric disorders

Nature genetics

2022/12

26. GENOME-WIDE ANALYSES OF VOCABULARY SIZE IN INFANCY AND TODDLERHOOD: LINKS WITH ADHD AND COGNITIVE TRAITS

European Neuropsychopharmacology

2022/10/1

White matter microstructural differences in children and genetic risk for multiple sclerosis: A population-based study

Multiple Sclerosis Journal

2022/4

Schizophrenia polygenic risk is associated with child mental health problems through early childhood adversity: evidence for a gene–environment correlation

European child & adolescent psychiatry

2022/3

The phenotypic spectrum and genotype-phenotype correlations in 106 patients with variants in major autism gene CHD8

Translational psychiatry

2022/10/1

Author Correction: Genome-wide meta-analysis of brain volume identifies genomic loci and genes shared with intelligence

Nature communications

2022

Response: No evidence for association between polygenic risk for multiple sclerosis and MRI phenotypes in approximately 30,000 healthy adult UK Biobank participants

Multiple Sclerosis Journal

2022/9

Genome-wide meta-analysis of insomnia prioritizes genes associated with metabolic and psychiatric pathways

Nature genetics

2022/8

See List of Professors in Philip Jansen University(Vrije Universiteit Amsterdam)