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Headache
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November 5, 1997
Wolff Award 1997. Involvement of a Ca2+ channel gene in familial hemiplegic migraine and migraine with and without aura. Dutch Migraine Genetics Research Group
R A Ophoff, G M Terwindt, M N Vergouwe, et al.
Cytogenetic and Genome Research
|
July 8, 2010
Recurrent inversion events at 17q21.31 microdeletion locus are linked to the MAPT H2 haplotype
P N Rao, W Li, L E L M Vissers, et al.
Behavior Genetics
|
March 17, 2010
"Forward genetics" as a method to maximize power and cost-efficiency in studies of human complex traits
M P M Boks, E M Derks, C V Dolan, et al.
European Journal of Pharmacology
|
February 15, 2001
The impact of pharmacogenetics for migraine
R A Ophoff, A M van den Maagdenberg, K I Roon, et al.
The Pharmacogenomics Journal
|
April 19, 2017
More than 25 years of genetic studies of clozapine-induced agranulocytosis
S A J de With, S L Pulit, W G Staal, et al.
European Journal of Human Genetics : EJHG
|
October 22, 1998
Migraine, ataxia and epilepsy: a challenging spectrum of genetically determined calcium channelopathies. Dutch Migraine Genetics Research Group
G M Terwindt, R A Ophoff, J Haan, et al.
Headache
|
May 22, 1998
5-HT1B receptor polymorphism and clinical response to sumatriptan
A MaassenVanDenBrink, M N Vergouwe, R A Ophoff, et al.
Clinical Neurology and Neurosurgery
|
August 1, 1994
Familial hemiplegic migraine in The Netherlands. Dutch Migraine Genetics Research Group
J Haan, G M Terwindt, P L Bos, et al.
International Journal of Epidemiology
|
November 1, 2007
Investigating gene environment interaction in complex diseases: increasing power by selective sampling for environmental exposure
M P M Boks, M Schipper, C D Schubart, et al.
Schizophrenia Research
|
March 11, 2008
The genetics of symptom dimensions of schizophrenia: review and meta-analysis
T Rietkerk, M P M Boks, I E Sommer, et al.
Page
of 7
Search research articles
Search
Showing results (11-20 of 68) with videos related to
Sort By:
Page
of 7
Headache
|
November 5, 1997
Wolff Award 1997. Involvement of a Ca2+ channel gene in familial hemiplegic migraine and migraine with and without aura. Dutch Migraine Genetics Research Group
R A Ophoff, G M Terwindt, M N Vergouwe, et al.
Cytogenetic and Genome Research
|
July 8, 2010
Recurrent inversion events at 17q21.31 microdeletion locus are linked to the MAPT H2 haplotype
P N Rao, W Li, L E L M Vissers, et al.
Behavior Genetics
|
March 17, 2010
"Forward genetics" as a method to maximize power and cost-efficiency in studies of human complex traits
M P M Boks, E M Derks, C V Dolan, et al.
European Journal of Pharmacology
|
February 15, 2001
The impact of pharmacogenetics for migraine
R A Ophoff, A M van den Maagdenberg, K I Roon, et al.
The Pharmacogenomics Journal
|
April 19, 2017
More than 25 years of genetic studies of clozapine-induced agranulocytosis
S A J de With, S L Pulit, W G Staal, et al.
European Journal of Human Genetics : EJHG
|
October 22, 1998
Migraine, ataxia and epilepsy: a challenging spectrum of genetically determined calcium channelopathies. Dutch Migraine Genetics Research Group
G M Terwindt, R A Ophoff, J Haan, et al.
Headache
|
May 22, 1998
5-HT1B receptor polymorphism and clinical response to sumatriptan
A MaassenVanDenBrink, M N Vergouwe, R A Ophoff, et al.
Clinical Neurology and Neurosurgery
|
August 1, 1994
Familial hemiplegic migraine in The Netherlands. Dutch Migraine Genetics Research Group
J Haan, G M Terwindt, P L Bos, et al.
International Journal of Epidemiology
|
November 1, 2007
Investigating gene environment interaction in complex diseases: increasing power by selective sampling for environmental exposure
M P M Boks, M Schipper, C D Schubart, et al.
Schizophrenia Research
|
March 11, 2008
The genetics of symptom dimensions of schizophrenia: review and meta-analysis
T Rietkerk, M P M Boks, I E Sommer, et al.
Page
of 7