D R Nyholt
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Explore the profile of D R Nyholt including associated specialties, affiliations and a list of published articles.
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34
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981
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Recent Articles
11.
Maher B, Kerr M, Cox H, MacMillan J, Brimage P, Esposito T, et al.
Neurogenetics
. 2012 Feb;
13(1):97-101.
PMID: 22294494
Investigations into migraine genetics have suggested that susceptibility loci exist on the X chromosome. These reports are supported by evidence that demonstrates male probands as having a higher proportion of...
12.
Wray N, Pergadia M, Blackwood D, Penninx B, Gordon S, Nyholt D, et al.
Mol Psychiatry
. 2010 Nov;
17(1):36-48.
PMID: 21042317
Major depressive disorder (MDD) is a common complex disorder with a partly genetic etiology. We conducted a genome-wide association study of the MDD2000+ sample (2431 cases, 3673 screened controls and...
13.
Cornes B, Lind P, Medland S, Montgomery G, Nyholt D, Martin N
Int J Obes (Lond)
. 2008 Nov;
33(1):75-9.
PMID: 19030008
Objective: To further investigate a common variant (rs9939609) in the fat mass- and obesity-associated gene (FTO), which recent genome-wide association studies have shown to be associated with body mass index...
14.
Holliday E, Mowry B, Nyholt D
Am J Med Genet B Neuropsychiatr Genet
. 2008 Mar;
147B(7):1080-8.
PMID: 18361422
The detection and replication of schizophrenia risk loci can require substantial sample sizes, which has prompted various collaborative efforts for combining multiple samples. However, pooled samples may comprise sub-samples with...
15.
Anttila V, Kallela M, Oswell G, Kaunisto M, Nyholt D, Hamalainen E, et al.
Am J Hum Genet
. 2006 Jun;
79(1):85-99.
PMID: 16773568
The commonly used "end diagnosis" phenotype that is adopted in linkage and association studies of complex traits is likely to represent an oversimplified model of the genetic background of a...
16.
Warner J, Nyholt D, Busfield F, Epstein M, Burgess J, Stranks S, et al.
J Med Genet
. 2006 Mar;
43(3):e12.
PMID: 16525030
Background: Familial isolated hyperparathyroidism (FIHP) is an autosomal dominantly inherited form of primary hyperparathyroidism. Although comprising only about 1% of cases of primary hyperparathyroidism, identification and functional analysis of a...
17.
Mah S, Nelson M, DeLisi L, Reneland R, Markward N, James M, et al.
Mol Psychiatry
. 2006 Jan;
11(5):471-8.
PMID: 16402134
The discovery of genetic factors that contribute to schizophrenia susceptibility is a key challenge in understanding the etiology of this disease. Here, we report the identification of a novel schizophrenia...
18.
A genome-wide scan provides evidence for loci influencing a severe heritable form of common migraine
Lea R, Nyholt D, Curtain R, Ovcaric M, Sciascia R, Bellis C, et al.
Neurogenetics
. 2005 Apr;
6(2):67-72.
PMID: 15830246
Migraine is a prevalent neurovascular disease with a significant genetic component. Linkage studies have so far identified migraine susceptibility loci on chromosomes 1, 4, 6, 11, 14, 19 and X....
19.
Evans D, Kirk K, Nyholt D, Novac C, Martin N
Br J Dermatol
. 2005 Mar;
152(3):579-81.
PMID: 15787839
No abstract available.
20.
Handoko H, Nyholt D, Hayward N, Nertney D, Hannah D, Windus L, et al.
Mol Psychiatry
. 2004 Oct;
10(6):589-97.
PMID: 15505638
Several lines of evidence have implicated the catechol-O-methyltransferase (COMT) gene as a candidate for schizophrenia (SZ) susceptibility, not only because it encodes a key dopamine catabolic enzyme but also because...