PubRank

T Foroud

Author PubWeight™ 120.25‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura. Nature 2001 6.95
2 Genome-wide search for genes affecting the risk for alcohol dependence. Am J Med Genet 1998 6.04
3 Localization of an ataxia-telangiectasia gene to chromosome 11q22-23. Nature 1988 3.82
4 Genome-wide association study of bipolar disorder in European American and African American individuals. Mol Psychiatry 2009 3.64
5 An autosomal genomic scan for loci linked to type II diabetes mellitus and body-mass index in Pima Indians. Am J Hum Genet 1998 3.16
6 A genome screen of maximum number of drinks as an alcoholism phenotype. Am J Med Genet 2000 3.14
7 LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8. Neurology 2007 2.86
8 Mutations in GBA are associated with familial Parkinson disease susceptibility and age at onset. Neurology 2008 2.73
9 Singleton deletions throughout the genome increase risk of bipolar disorder. Mol Psychiatry 2008 2.50
10 Joint multipoint linkage analysis of multivariate qualitative and quantitative traits. II. Alcoholism and event-related potentials. Am J Hum Genet 1999 2.23
11 An autosomal genomic scan for loci linked to prediabetic phenotypes in Pima Indians. J Clin Invest 1998 2.18
12 ADH1B is associated with alcohol dependence and alcohol consumption in populations of European and African ancestry. Mol Psychiatry 2011 2.05
13 Saccades in presymptomatic and early stages of Huntington disease. Neurology 2006 1.92
14 Enrichment of cis-regulatory gene expression SNPs and methylation quantitative trait loci among bipolar disorder susceptibility variants. Mol Psychiatry 2012 1.84
15 Autosomal genomic scan for loci linked to obesity and energy metabolism in Pima Indians. Am J Hum Genet 1998 1.78
16 A genome-wide search for genes that relate to a low level of response to alcohol. Alcohol Clin Exp Res 2001 1.72
17 Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene. Nat Genet 1992 1.66
18 Genome-wide association study of CSF biomarkers Abeta1-42, t-tau, and p-tau181p in the ADNI cohort. Neurology 2010 1.63
19 Linkage of structure at the proximal femur to chromosomes 3, 7, 8, and 19. J Bone Miner Res 2003 1.55
20 Localization of the gene for familial primary pulmonary hypertension to chromosome 2q31-32. Nat Genet 1997 1.52
21 Variation in GIGYF2 is not associated with Parkinson disease. Neurology 2009 1.47
22 Evidence for a locus on chromosome 1 that influences vulnerability to alcoholism and affective disorder. Am J Psychiatry 2001 1.46
23 Sibling pair linkage and association studies between bone mineral density and the insulin-like growth factor I gene locus. J Clin Endocrinol Metab 1999 1.45
24 Genome screen for QTLs contributing to normal variation in bone mineral density and osteoporosis. J Clin Endocrinol Metab 2000 1.43
25 Quantitative trait loci analysis of human event-related brain potentials: P3 voltage. Electroencephalogr Clin Neurophysiol 1998 1.43
26 Association of the kappa-opioid system with alcohol dependence. Mol Psychiatry 2006 1.42
27 Longitudinal cognitive and motor changes among presymptomatic Huntington disease gene carriers. Arch Neurol 1999 1.41
28 Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease. Neurology 2008 1.39
29 A quantitative trait locus for alcohol consumption in selectively bred rat lines. Alcohol Clin Exp Res 1998 1.37
30 Initial genome scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 4, 7, 9, 18, 19, 20, and 21q. Am J Med Genet 1997 1.36
31 Genomic screen for QTLs underlying alcohol consumption in the P and NP rat lines. Mamm Genome 1998 1.35
32 Subtle changes among presymptomatic carriers of the Huntington's disease gene. J Neurol Neurosurg Psychiatry 2000 1.32
33 Initial genomic scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 3, 5, 15, 16, 17, and 22. Am J Med Genet 1997 1.30
34 Whole-exome sequencing and imaging genetics identify functional variants for rate of change in hippocampal volume in mild cognitive impairment. Mol Psychiatry 2013 1.30
35 Progression of symptoms in the early and middle stages of Huntington disease. Arch Neurol 2001 1.30
36 A primary linkage map of the human chromosome 11q22-23 region. Genomics 1990 1.25
37 Amplitude of visual P3 event-related potential as a phenotypic marker for a predisposition to alcoholism: preliminary results from the COGA Project. Collaborative Study on the Genetics of Alcoholism. Alcohol Clin Exp Res 1998 1.22
38 A genome-wide association study of alcohol-dependence symptom counts in extended pedigrees identifies C15orf53. Mol Psychiatry 2012 1.21
39 Prenatal alcohol exposure alters the patterns of facial asymmetry. Alcohol 2010 1.21
40 Confirmation of subtle motor changes among presymptomatic carriers of the Huntington disease gene. Arch Neurol 2000 1.19
41 Linkage of a QTL contributing to normal variation in bone mineral density to chromosome 11q12-13. J Bone Miner Res 1998 1.18
42 Genomewide search for genes influencing percent body fat in Pima Indians: suggestive linkage at chromosome 11q21-q22. Pima Diabetes Gene Group. Am J Hum Genet 1997 1.17
43 Genome screen for quantitative trait loci underlying normal variation in femoral structure. J Bone Miner Res 2001 1.16
44 Initial genome screen for bipolar disorder in the NIMH genetics initiative pedigrees: chromosomes 2, 11, 13, 14, and X. Am J Med Genet 1997 1.15
45 Motor changes in presymptomatic Huntington disease gene carriers. Arch Neurol 1996 1.14
46 Identification of a quantitative trait locus on rat chromosome 4 that is strongly linked to femoral neck structure and strength. Bone 2006 1.12
47 The ATC (ataxia-telangiectasia complementation group C) locus localizes to 11q22-q23. Genomics 1991 1.11
48 Anxiety proneness linked to epistatic loci in genome scan of human personality traits. Am J Med Genet 1998 1.11
49 Genetics of event-related brain potentials in response to a semantic priming paradigm in families with a history of alcoholism. Am J Hum Genet 2000 1.11
50 Initial genome scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 1, 6, 8, 10, and 12. Am J Med Genet 1997 1.10
51 Further mapping of an ataxia-telangiectasia locus to the chromosome 11q23 region. Am J Hum Genet 1990 1.10
52 Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations. Neurology 2009 1.10
53 Linkage stratification and mutation analysis at the Parkin locus identifies mutation positive Parkinson's disease families. J Med Genet 2002 1.09
54 Variability in skeletal mass, structure, and biomechanical properties among inbred strains of rats. J Bone Miner Res 2001 1.09
55 A genome-wide screen for genes influencing conduct disorder. Mol Psychiatry 2004 1.07
56 Automated diagnosis of fetal alcohol syndrome using 3D facial image analysis. Orthod Craniofac Res 2008 1.04
57 Genes influencing Parkinson disease onset: replication of PARK3 and identification of novel loci. Neurology 2004 1.01
58 Genotype patterns at PICALM, CR1, BIN1, CLU, and APOE genes are associated with episodic memory. Neurology 2012 0.99
59 Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17. Am J Hum Genet 1997 0.99
60 Family-based study of the association of the dopamine D2 receptor gene (DRD2) with habitual smoking. Am J Med Genet 2000 0.98
61 Family-based genome-wide association study of frontal θ oscillations identifies potassium channel gene KCNJ6. Genes Brain Behav 2012 0.98
62 Possible localization of a major gene for cleft lip and palate to 4q. Clin Genet 1994 0.98
63 Functional relevance of human adh polymorphism. Alcohol Clin Exp Res 2001 0.95
64 Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms. Mol Psychiatry 2011 0.93
65 Chromosome 6 workshop report. Am J Med Genet 1999 0.92
66 A sex-adjusted and age-adjusted genome screen for nested alcohol dependence diagnoses. Psychiatr Genet 2005 0.92
67 A family-based analysis of the association of the dopamine D2 receptor (DRD2) with alcoholism. Alcohol Clin Exp Res 1998 0.90
68 A family-based analysis of whether the functional promoter alleles of the serotonin transporter gene HTT affect the risk for alcohol dependence. Alcohol Clin Exp Res 1998 0.89
69 Confirmation of linkage of limb-girdle muscular dystrophy, type 2, to chromosome 15. Genomics 1992 0.88
70 Independent and epistatic effects of variants in VPS10-d receptors on Alzheimer disease risk and processing of the amyloid precursor protein (APP). Transl Psychiatry 2013 0.88
71 Genetics of bipolar affective disorder. Curr Psychiatry Rep 2000 0.86
72 Heterogeneity in hereditary pancreatitis. Am J Med Genet 1998 0.84
73 Stoppage: an issue for segregation analysis. Genet Epidemiol 2001 0.83
74 The North American Multiple System Atrophy Study Group. J Neural Transm (Vienna) 2005 0.81
75 Update on chromosomal locations for psychiatric disorders: report of the interim meeting of chromosome workshop chairpersons from the VIIth World Congress of Psychiatric Genetics, Monterey, California, October 14-18, 1999. Am J Med Genet 2000 0.81
76 Common biological networks underlie genetic risk for alcoholism in African- and European-American populations. Genes Brain Behav 2013 0.81
77 Use of variable marker density, principal components, and neural networks in the dissection of disease etiology. Genet Epidemiol 2001 0.80
78 Identification of functional variants from whole-exome sequencing, combined with neuroimaging genetics. Mol Psychiatry 2013 0.80
79 Spheroid body myopathy revisited. Muscle Nerve 1997 0.79
80 Locus heterogeneity of autosomal dominant osteopetrosis (ADO). J Clin Endocrinol Metab 1999 0.79
81 Age at intracranial aneurysm rupture among generations: Familial Intracranial Aneurysm Study. Neurology 2009 0.76
82 Genome screen for platelet monoamine oxidase (MAO) activity. Am J Med Genet 1999 0.76
83 Chromosome 6 workshop. Psychiatr Genet 1998 0.75
84 Parametric linkage analysis and disequilibrium methods to identify loci for complex disease. Genet Epidemiol 2001 0.75
85 Linkage of type II and type III cystinuria to 19q13.1: codominant inheritance of two cystinuric alleles at 19q13.1 produces an extreme stone-forming phenotype. Am J Med Genet 1999 0.75
86 Sib pair linkage and association studies between bone mineral density and the interleukin-6 gene locus. Bone 2000 0.75
87 Nonparametric linkage and family-based association studies of a simulated complex disorder. Genet Epidemiol 1999 0.75
88 Gene mapping using linkage analysis. Turk J Pediatr 1993 0.75