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
21.
Li W, Nyholt D
Genet Epidemiol
. 2002 Jan;
21 Suppl 1:S272-7.
PMID: 11793681
We carried out a discriminant analysis with identity by descent (IBD) at each marker as inputs, and the sib pair type (affected-affected versus affected-unaffected) as the output. Using simple logistic...
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23.
Liu J, Nyholt D, Magnussen P, Parano E, Pavone P, Geschwind D, et al.
Am J Hum Genet
. 2001 Jul;
69(2):327-40.
PMID: 11452361
We report the analysis of 335 microsatellite markers genotyped in 110 multiplex families with autism. All families include at least two "affected" siblings, at least one of whom has autism;...
24.
Simonic I, Nyholt D, Gericke G, Gordon D, Matsumoto N, Ledbetter D, et al.
Am J Med Genet
. 2001 Apr;
105(2):163-7.
PMID: 11304830
Utilizing DNA samples from 91 Afrikaner nuclear families with one or more affected children, five genomic regions on chromosomes 2p, 8q, 11q, 20q, and 21q that gave evidence for association...
25.
Nyholt D, Curtain R, Griffiths L
Hum Genet
. 2000 Sep;
107(1):18-23.
PMID: 10982029
In a previous study we found evidence for an X-linked genetic component for familial typical migraine in two large Australian white pedigrees, designated MF7 and MF14. Significant excess allele sharing...
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27.
Wang W, Glenn C, Zhang W, Benjafield A, Nyholt D, Morris B
Am J Med Genet
. 1999 Oct;
87(1):53-60.
PMID: 10528248
Linkage with essential hypertension has been claimed for a microsatellite marker near the angiotensinogen gene (AGT; chromosome 1q42), as has association for the AGT variants M235T, G(-6)A and A(-20)C. To...
28.
Benjafield A, Jeyasingam C, Nyholt D, Griffiths L, Morris B
Hypertension
. 1998 Dec;
32(6):1094-7.
PMID: 9856980
-Essential hypertensives display enhanced signal transduction through pertussis toxin-sensitive G proteins. The T allele of a C825T variant in exon 10 of the G protein beta3 subunit gene (GNB3) induces...
29.
Nyholt D, Lea R, Goadsby P, Brimage P, Griffiths L
Neurology
. 1998 May;
50(5):1428-32.
PMID: 9596000
Migraine is a frequent familial disorder that, in common with most multifactorial disorders, has an unknown etiology. The authors identified several families with multiple individuals affected by typical migraine using...
30.
Nyholt D, Dawkins J, Brimage P, Goadsby P, Nicholson G, Griffiths L
Hum Mol Genet
. 1998 Apr;
7(3):459-63.
PMID: 9467004
Migraine is a common complex disorder that shows strong familial aggregation. There is a general increased prevalence of migraine in females compared with males, with recent studies indicating that migraine...