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Bjpsych Open
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December 9, 2020
Phenome-wide and genome-wide analyses of quality of life in schizophrenia
Raha Pazoki, Bochao Danae Lin, Kristel R van Eijk, et al.
Neurology
|
May 5, 1998
Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine. Dutch Migraine Genetics Research Group
G M Terwindt, R A Ophoff, J Haan, et al.
British Journal of Cancer
|
August 23, 2000
Prevalence of BRCA1 in a hospital-based population of Dutch breast cancer patients
H Papelard, G H de Bock, R van Eijk, et al.
The British Journal of Dermatology
|
October 14, 2014
Diagnostic and prognostic significance of CDKN2A/CDKN2B deletions in patients with transformed mycosis fungoides and primary cutaneous CD30-positive lymphoproliferative disease
A R Nicolae-Cristea, M F Benner, W H Zoutman, et al.
Genetic Epidemiology
|
February 24, 2009
Using genome-wide pathway analysis to unravel the etiology of complex diseases
Clara C Elbers, Kristel R van Eijk, Lude Franke, et al.
Neurology
|
April 26, 2001
Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura
G M Terwindt, R A Ophoff, R van Eijk, et al.
Schizophrenia Bulletin
|
November 25, 2015
DRD2 Schizophrenia-Risk Allele Is Associated With Impaired Striatal Functioning in Unaffected Siblings of Schizophrenia Patients
Matthijs Vink, Max de Leeuw, Jurjen J Luykx, et al.
European Journal of Human Genetics : EJHG
|
November 27, 2014
Identification of schizophrenia-associated loci by combining DNA methylation and gene expression data from whole blood
Kristel R van Eijk, Simone de Jong, Eric Strengman, et al.
Psychological Medicine
|
January 7, 2022
Polygenic risk, familial liability and stress reactivity in psychosis: an experience sampling study
Anita Schick, Ruud van Winkel, Bochao D Lin, et al.
Genomics
|
July 1, 1994
Genetic heterogeneity of familial hemiplegic migraine
R A Ophoff, R van Eijk, L A Sandkuijl, et al.
Page
of 9
Search research articles
Search
Showing results (11-20 of 89) with videos related to
Sort By:
Page
of 9
Bjpsych Open
|
December 9, 2020
Phenome-wide and genome-wide analyses of quality of life in schizophrenia
Raha Pazoki, Bochao Danae Lin, Kristel R van Eijk, et al.
Neurology
|
May 5, 1998
Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine. Dutch Migraine Genetics Research Group
G M Terwindt, R A Ophoff, J Haan, et al.
British Journal of Cancer
|
August 23, 2000
Prevalence of BRCA1 in a hospital-based population of Dutch breast cancer patients
H Papelard, G H de Bock, R van Eijk, et al.
The British Journal of Dermatology
|
October 14, 2014
Diagnostic and prognostic significance of CDKN2A/CDKN2B deletions in patients with transformed mycosis fungoides and primary cutaneous CD30-positive lymphoproliferative disease
A R Nicolae-Cristea, M F Benner, W H Zoutman, et al.
Genetic Epidemiology
|
February 24, 2009
Using genome-wide pathway analysis to unravel the etiology of complex diseases
Clara C Elbers, Kristel R van Eijk, Lude Franke, et al.
Neurology
|
April 26, 2001
Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura
G M Terwindt, R A Ophoff, R van Eijk, et al.
Schizophrenia Bulletin
|
November 25, 2015
DRD2 Schizophrenia-Risk Allele Is Associated With Impaired Striatal Functioning in Unaffected Siblings of Schizophrenia Patients
Matthijs Vink, Max de Leeuw, Jurjen J Luykx, et al.
European Journal of Human Genetics : EJHG
|
November 27, 2014
Identification of schizophrenia-associated loci by combining DNA methylation and gene expression data from whole blood
Kristel R van Eijk, Simone de Jong, Eric Strengman, et al.
Psychological Medicine
|
January 7, 2022
Polygenic risk, familial liability and stress reactivity in psychosis: an experience sampling study
Anita Schick, Ruud van Winkel, Bochao D Lin, et al.
Genomics
|
July 1, 1994
Genetic heterogeneity of familial hemiplegic migraine
R A Ophoff, R van Eijk, L A Sandkuijl, et al.
Page
of 9