PubRank

Pak Sham

Author PubWeight™ 113.23‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Properties of structured association approaches to detecting population stratification. Hum Hered 2004 7.53
2 Parental phenotypes in family-based association analysis. Am J Hum Genet 2004 6.35
3 Ascertainment through family history of disease often decreases the power of family-based association studies. Behav Genet 2007 6.06
4 The heritability of bipolar affective disorder and the genetic relationship to unipolar depression. Arch Gen Psychiatry 2003 5.15
5 Rates of adult schizophrenia following prenatal exposure to the Chinese famine of 1959-1961. JAMA 2005 3.83
6 Prevalence and pattern of lumbar magnetic resonance imaging changes in a population study of one thousand forty-three individuals. Spine (Phila Pa 1976) 2009 2.56
7 Relapse prevention in patients with bipolar disorder: cognitive therapy outcome after 2 years. Am J Psychiatry 2005 2.33
8 Meta-analysis of the P300 and P50 waveforms in schizophrenia. Schizophr Res 2004 2.30
9 A developmental model for similarities and dissimilarities between schizophrenia and bipolar disorder. Schizophr Res 2004 2.24
10 Substantial genetic overlap between neurocognition and schizophrenia: genetic modeling in twin samples. Arch Gen Psychiatry 2007 2.04
11 Reaction time performance in ADHD: improvement under fast-incentive condition and familial effects. Psychol Med 2007 1.85
12 A randomized controlled study of cognitive therapy for relapse prevention for bipolar affective disorder: outcome of the first year. Arch Gen Psychiatry 2003 1.84
13 Regional volume deviations of brain structure in schizophrenia and psychotic bipolar disorder: computational morphometry study. Br J Psychiatry 2005 1.83
14 A behavioural genomic analysis of DNA markers associated with general cognitive ability in 7-year-olds. J Child Psychol Psychiatry 2005 1.62
15 Cognitive style in bipolar disorder. Br J Psychiatry 2005 1.55
16 DSM-IV combined type ADHD shows familial association with sibling trait scores: a sampling strategy for QTL linkage. Am J Med Genet B Neuropsychiatr Genet 2008 1.50
17 Substantial shared genetic influences on schizophrenia and event-related potentials. Am J Psychiatry 2007 1.48
18 Optimal selection strategies for QTL mapping using pooled DNA samples. Eur J Hum Genet 2002 1.45
19 Meta-analysis of magnetic resonance imaging brain morphometry studies in bipolar disorder. Biol Psychiatry 2004 1.45
20 A meta-analysis of association studies between the 10-repeat allele of a VNTR polymorphism in the 3'-UTR of dopamine transporter gene and attention deficit hyperactivity disorder. Am J Med Genet B Neuropsychiatr Genet 2007 1.36
21 Meta-analysis of genome-wide linkage studies in BMI and obesity. Obesity (Silver Spring) 2007 1.32
22 Gray matter in first-episode schizophrenia before and after antipsychotic drug treatment. Anatomical likelihood estimation meta-analyses with sample size weighting. Schizophr Bull 2009 1.26
23 Evidence that RNA editing modulates splice site selection in the 5-HT2C receptor gene. Nucleic Acids Res 2004 1.26
24 Whole genome linkage scan of recurrent depressive disorder from the depression network study. Hum Mol Genet 2005 1.25
25 Association of the Taq I allele in vitamin D receptor with degenerative disc disease and disc bulge in a Chinese population. Spine (Phila Pa 1976) 2006 1.24
26 Association of the asporin D14 allele with lumbar-disc degeneration in Asians. Am J Hum Genet 2008 1.22
27 Heritability and reliability of P300, P50 and duration mismatch negativity. Behav Genet 2006 1.22
28 Adjusting for covariates in variance components QTL linkage analysis. Behav Genet 2004 1.20
29 Genetics of disc degeneration. Eur Spine J 2006 1.20
30 Sense of hyper-positive self and response to cognitive therapy in bipolar disorder. Psychol Med 2005 1.16
31 Impaired intellect and memory: a missing link between genetic risk and schizophrenia? Arch Gen Psychiatry 2010 1.15
32 A1166C genetic variation of the angiotensin II type I receptor gene and susceptibility to coronary heart disease: collaborative of 53 studies with 20,435 cases and 23,674 controls. Atherosclerosis 2010 1.13
33 The early auditory gamma-band response is heritable and a putative endophenotype of schizophrenia. Schizophr Bull 2009 1.13
34 The p.Ser267Phe variant in SLC10A1 is associated with resistance to chronic hepatitis B. Hepatology 2015 1.12
35 Joint analysis of the DRD5 marker concludes association with attention-deficit/hyperactivity disorder confined to the predominantly inattentive and combined subtypes. Am J Hum Genet 2004 1.12
36 Prenatal malnutrition and adult schizophrenia: further evidence from the 1959-1961 Chinese famine. Schizophr Bull 2009 1.11
37 Autistic disorders and schizophrenia: related or remote? An anatomical likelihood estimation. PLoS One 2010 1.10
38 Parental familial vulnerability, family environment, and their interactions as predictors of depressive symptoms in adolescents. J Am Acad Child Adolesc Psychiatry 2004 1.09
39 SNP rs11190870 near LBX1 is associated with adolescent idiopathic scoliosis in southern Chinese. J Hum Genet 2012 1.07
40 A controlled study of brain structure in monozygotic twins concordant and discordant for schizophrenia. Biol Psychiatry 2004 1.05
41 The emerging molecular architecture of schizophrenia, polygenic risk scores and the clinical implications for GxE research. Soc Psychiatry Psychiatr Epidemiol 2014 1.05
42 DNA pooling analysis of 21 norepinephrine transporter gene SNPs with attention deficit hyperactivity disorder: no evidence for association. Am J Med Genet B Neuropsychiatr Genet 2005 1.04
43 Design and analysis of association studies using pooled DNA from large twin samples. Behav Genet 2006 1.01
44 Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settings. Biol Psychiatry 2008 0.98
45 Quantitative trait locus analysis of candidate gene alleles associated with attention deficit hyperactivity disorder (ADHD) in five genes: DRD4, DAT1, DRD5, SNAP-25, and 5HT1B. Am J Med Genet B Neuropsychiatr Genet 2005 0.98
46 Abnormal P300 in people with high risk of developing psychosis. Neuroimage 2008 0.96
47 Identification of genes with allelic imbalance on 6p associated with nasopharyngeal carcinoma in southern Chinese. PLoS One 2011 0.94
48 Variance components models for gene-environment interaction in quantitative trait locus linkage analysis. Twin Res 2002 0.93
49 Brain volumes in familial and non-familial schizophrenic probands and their unaffected relatives. Am J Med Genet 2002 0.93
50 Toward the proteomic identification of biomarkers for the prediction of HBV related hepatocellular carcinoma. J Cell Biochem 2008 0.93
51 Genetic overlap between P300, P50, and duration mismatch negativity. Am J Med Genet B Neuropsychiatr Genet 2006 0.92
52 The serotonin transporter gene as a QTL for ADHD. Am J Med Genet B Neuropsychiatr Genet 2005 0.92
53 Neuregulin-1 and the P300 waveform--a preliminary association study using a psychosis endophenotype. Schizophr Res 2008 0.92
54 Genetic overlap between bipolar illness and event-related potentials. Psychol Med 2007 0.91
55 Hippocampal volume in familial and nonfamilial schizophrenic probands and their unaffected relatives. Biol Psychiatry 2003 0.91
56 Positional pathway screen of wnt signaling genes in schizophrenia: association with DKK4. Biol Psychiatry 2007 0.89
57 Association between promoter -1607 polymorphism of MMP1 and lumbar disc disease in Southern Chinese. BMC Med Genet 2008 0.89
58 Further evidence for shared genetic effects between psychotic bipolar disorder and P50 suppression: a combined twin and family study. Am J Med Genet B Neuropsychiatr Genet 2008 0.87
59 Linkage disequilibrium analysis of the CHRNA7 gene and its partially duplicated region in schizophrenia. Neurosci Res 2006 0.87
60 The differential clinical and neurocognitive profiles of COMT SNP rs165599 genotypes in schizophrenia. J Int Neuropsychol Soc 2005 0.86
61 An association analysis of microsatellite markers across the Prader-Willi/Angelman critical region on chromosome 15 (q11-13) and autism spectrum disorder. Am J Med Genet B Neuropsychiatr Genet 2005 0.85
62 Family-based association tests for quantitative traits using pooled DNA. Eur J Hum Genet 2002 0.84
63 The genetic and environmental influences of event-related gamma oscillations on bipolar disorder. Bipolar Disord 2011 0.83
64 Haplotype and linkage disequilibrium analysis to characterise a region in the calcium channel gene CACNA1A associated with idiopathic generalised epilepsy. Eur J Hum Genet 2002 0.83
65 Normal cerebral asymmetry in familial and non-familial schizophrenic probands and their unaffected relatives. Schizophr Res 2004 0.83
66 Frontal-subcortical protein expression following prenatal exposure to maternal inflammation. PLoS One 2011 0.82
67 Association of the serotonin transporter gene, neuroticism and smoking behaviours. J Hum Genet 2008 0.81
68 Familiality of clinical characteristics in schizophrenia. J Psychiatr Res 2002 0.81
69 Validation of single nucleotide polymorphism quantification in pooled DNA samples with SNaPIT. A glycosylase-mediated methods for polymorphism detection method. Mol Biotechnol 2002 0.81
70 Cerebral asymmetry in 14 year olds born very preterm. Brain Res 2006 0.80
71 The relationship between predisposing factors, premorbid function and symptom dimensions in psychosis: an integrated approach. Eur Psychiatry 2002 0.80
72 Cognitive style, personality and vulnerability to postnatal depression. Br J Psychiatry 2010 0.80
73 Intellectual asymmetry and genetic liability in first-degree relatives of probands with schizophrenia. Br J Psychiatry 2006 0.80
74 Association of ICAM3 genetic variant with severe acute respiratory syndrome. J Infect Dis 2007 0.79
75 The value of four mental health self-report scales in predicting interview-based mood and anxiety disorder diagnoses in sibling pairs. Twin Res Hum Genet 2005 0.79
76 Soluble interleukin 2 receptor levels in families of people with schizophrenia. Schizophr Res 2002 0.78
77 Meta-analyses of genome-wide linkage scans of anxiety-related phenotypes. Eur J Hum Genet 2012 0.78
78 MRI predicts remission at 1 year in first-episode schizophrenia in females with larger striato-thalamic volumes. Neuropsychobiology 2014 0.77
79 CHIP: Defining a dimension of the vulnerability to attention deficit hyperactivity disorder (ADHD) using sibling and individual data of children in a community-based sample. Am J Med Genet B Neuropsychiatr Genet 2003 0.76
80 Risky drinking by both sexes should be tackled. BMJ 2002 0.75
81 iCartiGD: the Integrated Cartilage Gene Database. BMC Genet 2007 0.75
82 The contribution of risk factors to blood pressure heritability estimates in young adults: the East flanders prospective twin study. Twin Res 2004 0.75
83 Pathway-based Single-Cell RNA-Seq Classification, Clustering, and Construction of Gene-Gene Interactions Networks Using Random Forests. IEEE J Biomed Health Inform 2019 0.75