PubRank
Search
About
S G Schwab
Author PubWeight™ 27.82
‹?›
Top papers
Rank
Title
Journal
Year
PubWeight™
‹?›
1
Meta-analysis of 32 genome-wide linkage studies of schizophrenia.
Mol Psychiatry
2008
2.07
2
Genotype-phenotype relationship in female carriers of the premutation and full mutation of FMR-1.
Psychiatry Res
1998
1.95
3
Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III.
Am J Hum Genet
2000
1.68
4
Genetic investigation of chromosome 5q GABAA receptor subunit genes in schizophrenia.
Mol Psychiatry
2005
1.34
5
Haplotypic association spanning the 22q11.21 genes COMT and ARVCF with schizophrenia.
Mol Psychiatry
2005
1.17
6
KIBRA genetic polymorphism influences episodic memory in later life, but does not increase the risk of mild cognitive impairment.
J Cell Mol Med
2008
1.17
7
Fragile-X carrier females: evidence for a distinct psychopathological phenotype?
Am J Med Genet
1996
1.12
8
Genomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphisms.
Mol Psychiatry
2009
0.99
9
Multicenter linkage study of schizophrenia loci on chromosome 22q.
Mol Psychiatry
2004
0.98
10
Support for allelic association of a polymorphic site in the promoter region of the serotonin transporter gene with risk for alcohol dependence.
Am J Psychiatry
2000
0.96
11
Do schizophrenia and affective disorder share susceptibility genes?
Schizophr Res
1999
0.95
12
Allelic association between the D10S1423 marker and Alzheimer's disease in a German population.
Neurosci Lett
2000
0.90
13
Genetic polymorphism of cathepsin D is strongly associated with the risk for developing sporadic Alzheimer's disease.
Neurosci Lett
1999
0.89
14
Genome-wide scan in 124 Indonesian sib-pair families with schizophrenia reveals genome-wide significant linkage to a locus on chromosome 3p26-21.
Am J Med Genet B Neuropsychiatr Genet
2008
0.88
15
Association analysis of NOTCH4 loci in schizophrenia using family and population-based controls.
Nat Genet
2001
0.81
16
DAT1 gene polymorphism in alcoholism: a family-based association study.
Biol Psychiatry
1999
0.80
17
Association between hSKCa3 and schizophrenia not confirmed by transmission disequilibrium test in 193 offspring/parents trios.
Mol Psychiatry
1999
0.79
18
Early-onset and late-onset depression are independent of the genetic polymorphism of apolipoprotein E.
Dement Geriatr Cogn Disord
1999
0.79
19
Chromosome 8 workshop.
Psychiatr Genet
1998
0.79
20
No evidence for segregation distortion in females in a sample of 72 families with schizophrenia with potential linkage to chromosome 10p14-p11.
Am J Med Genet
1999
0.79
21
No association between an intronic polymorphism in the presenilin-1 gene and Alzheimer disease in a German population.
J Neurol Sci
1999
0.79
22
Association of PIP5K2A with schizophrenia: a study in an indonesian family sample.
Am J Med Genet B Neuropsychiatr Genet
2008
0.78
23
Chromosomes 8 and 10 workshop.
Am J Med Genet
1999
0.78
24
Serotonin transporter gene and schizophrenia: evidence for association/linkage disequilibrium in families with affected siblings.
Mol Psychiatry
2000
0.78
25
Evaluation of association of SNPs in the TNF alpha gene region with schizophrenia.
Am J Med Genet B Neuropsychiatr Genet
2007
0.78
26
Disturbed copper transport in humans. Part 2: mutations of the ATP7B gene lead to Wilson disease (WD).
Cell Mol Biol (Noisy-le-grand)
2001
0.77
27
Excess of homozygosity at the dopamine D3 receptor gene in schizophrenia not confirmed.
J Med Genet
1993
0.77
28
Lack of linkage between schizophrenia and markers at the telomeric end of the pseudoautosomal region of the sex chromosomes.
Biol Psychiatry
1995
0.77
29
Searching for susceptibility genes in schizophrenia by genetic linkage analysis.
Cold Spring Harb Symp Quant Biol
1996
0.75
30
Copper genes are not implicated in the pathogenesis of focal dystonia.
Neurology
2002
0.75
31
[Serotonin transporter gene and stress reactivity in unipolar depression. Role of the HPA system as endophenotype of the SLC6A4 gene].
Nervenarzt
2014
0.75
32
Presymptomatic testing in families with Wilson's disease.
Lancet
1994
0.75