PubRank

Anne S Bassett

Author PubWeight™ 86.25‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data. Nucleic Acids Res 2007 10.08
2 Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia. Am J Hum Genet 2003 6.63
3 Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene. Am J Hum Genet 2008 2.84
4 Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome. Am J Psychiatry 2014 2.15
5 A method for accurate detection of genomic microdeletions using real-time quantitative PCR. BMC Genomics 2005 2.04
6 Clinical and genetic epidemiology of Bardet-Biedl syndrome in Newfoundland: a 22-year prospective, population-based, cohort study. Am J Med Genet A 2005 2.03
7 Neurocognitive profile in 22q11 deletion syndrome and schizophrenia. Schizophr Res 2006 1.89
8 Identification of a schizophrenia-associated functional noncoding variant in NOS1AP. Am J Psychiatry 2009 1.85
9 The impact of implantable cardioverter-defibrillator therapy on survival in autosomal-dominant arrhythmogenic right ventricular cardiomyopathy (ARVD5). J Am Coll Cardiol 2005 1.83
10 The co-occurrence of early onset Parkinson disease and 22q11.2 deletion syndrome. Am J Med Genet A 2009 1.82
11 Association between early-onset Parkinson disease and 22q11.2 deletion syndrome: identification of a novel genetic form of Parkinson disease and its clinical implications. JAMA Neurol 2013 1.81
12 A major susceptibility locus for specific language impairment is located on 13q21. Am J Hum Genet 2002 1.79
13 Linkage disequilibrium mapping of schizophrenia susceptibility to the CAPON region of chromosome 1q22. Am J Hum Genet 2004 1.55
14 Incomplete knowledge of the clinical context as a barrier to interpreting incidental genetic research findings. Am J Bioeth 2013 1.48
15 Rare copy number variations in adults with tetralogy of Fallot implicate novel risk gene pathways. PLoS Genet 2012 1.44
16 Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarrays. Hum Mol Genet 2013 1.44
17 Structural brain abnormalities in patients with schizophrenia and 22q11 deletion syndrome. Biol Psychiatry 2002 1.27
18 1q21.1 Microduplication expression in adults. Genet Med 2012 1.25
19 Molecular characterization of deletion breakpoints in adults with 22q11 deletion syndrome. Hum Genet 2006 1.17
20 Sex differences in reproductive fitness contribute to preferential maternal transmission of 22q11.2 deletions. J Med Genet 2011 1.13
21 Extracardiac features predicting 22q11.2 deletion syndrome in adult congenital heart disease. Int J Cardiol 2008 1.12
22 Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures. Hum Mol Genet 2013 1.11
23 Childhood head injury and expression of schizophrenia in multiply affected families. Arch Gen Psychiatry 2003 1.08
24 Evaluating genetic counseling for family members of individuals with schizophrenia in the molecular age. Schizophr Bull 2012 1.08
25 Expression of autism spectrum and schizophrenia in patients with a 22q11.2 deletion. Schizophr Res 2012 1.08
26 Clinical applications of schizophrenia genetics: genetic diagnosis, risk, and counseling in the molecular era. Appl Clin Genet 2012 1.07
27 Fine mapping of the schizophrenia susceptibility locus on chromosome 1q22. Hum Hered 2002 1.06
28 Genotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients. Hum Mutat 2011 1.05
29 Association of schizophrenia in 22q11.2 deletion syndrome and gray matter volumetric deficits in the superior temporal gyrus. Am J Psychiatry 2011 1.03
30 Association of the PIK4CA schizophrenia-susceptibility gene in adults with the 22q11.2 deletion syndrome. Am J Med Genet B Neuropsychiatr Genet 2009 1.02
31 Recognizing a common genetic syndrome: 22q11.2 deletion syndrome. CMAJ 2008 1.01
32 Evaluation of a susceptibility gene for schizophrenia: genotype based meta-analysis of RGS4 polymorphisms from thirteen independent samples. Biol Psychiatry 2006 1.00
33 Hippocampal malrotation is associated with chromosome 22q11.2 microdeletion. Can J Neurol Sci 2013 0.99
34 Heritability of neurocognitive traits in familial schizophrenia. Am J Med Genet B Neuropsychiatr Genet 2009 0.97
35 Evaluating genetic counseling for individuals with schizophrenia in the molecular age. Schizophr Bull 2012 0.96
36 miRNA-mediated risk for schizophrenia in 22q11.2 deletion syndrome. Front Genet 2012 0.96
37 The ever-evolving concept of clinical significance and the potential for sins of omission in genetic research. Am J Bioeth 2012 0.95
38 Functional outcomes of adults with 22q11.2 deletion syndrome. Genet Med 2012 0.94
39 22q11.2 deletion syndrome: attitudes towards disclosing the risk of psychiatric illness. J Genet Couns 2012 0.93
40 Increasing genotype-phenotype model determinism: application to bivariate reading/language traits and epistatic interactions in language-impaired families. Hum Hered 2010 0.92
41 Movement disorders and other motor abnormalities in adults with 22q11.2 deletion syndrome. Am J Med Genet A 2015 0.91
42 Premorbid adjustment and schizophrenia in individuals with 22q11.2 deletion syndrome. Schizophr Res 2013 0.90
43 Patterns of cardiac and extracardiac anomalies in adults with tetralogy of fallot. Am Heart J 2011 0.90
44 Childhood trauma and genetic factors in familial schizophrenia associated with the NOS1AP gene. Schizophr Res 2010 0.89
45 Voxel-based morphometry and automated lobar volumetry: the trade-off between spatial scale and statistical correction. Neuroimage 2009 0.87
46 Phenotype matters: the case for careful characterization of relevant traits. Am J Psychiatry 2008 0.87
47 Prenatal genetic testing with chromosomal microarray analysis identifies major risk variants for schizophrenia and other later-onset disorders. Am J Psychiatry 2013 0.86
48 13q13.1-q13.2 deletion in tetralogy of Fallot: clinical report and a literature review. Int J Cardiol 2010 0.84
49 Heritability of schizophrenia and major affective disorder as a function of age, in the presence of strong cohort effects. Eur Arch Psychiatry Clin Neurosci 2005 0.84
50 Genetic covariation underlying reading, language and related measures in a sample selected for specific language impairment. Behav Genet 2010 0.83
51 Parental origin, DNA structure, and the schizophrenia spectrum. Am J Psychiatry 2011 0.83
52 Prevalence of hypocalcaemia and its associated features in 22q11·2 deletion syndrome. Clin Endocrinol (Oxf) 2014 0.83
53 Complex congenital heart disease in unaffected relatives of adults with 22q11.2 deletion syndrome. Am J Cardiol 2011 0.82
54 Genetic predictors of response to treatment with citalopram in depression secondary to traumatic brain injury. Brain Inj 2010 0.82
55 Early environmental exposures influence schizophrenia expression even in the presence of strong genetic predisposition. Schizophr Res 2012 0.81
56 Adult neuropsychiatric expression and familial segregation of 2q13 duplications. Am J Med Genet B Neuropsychiatr Genet 2014 0.80
57 Overt cleft palate phenotype and TBX1 genotype correlations in velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients. Am J Med Genet A 2012 0.79
58 Reduced gray matter in the anterior cingulate gyrus in familial schizophrenia: a preliminary report. Schizophr Res 2010 0.77
59 Reproductive genetic testing and human genetic variation in the era of genomic medicine. Am J Bioeth 2015 0.77
60 PERSONALITY FEATURES AND DISORDER IN THE SUBJECTS IN THE NEW YORK HIGH-RISK PROJECT. J Psychiatr Res 1993 0.77
61 Individualizing recurrence risks for severe mental illness: epidemiologic and molecular genetic approaches. Schizophr Bull 2013 0.76
62 Reproductive fitness and genetic transmission of tetralogy of Fallot in the molecular age. Circ Cardiovasc Genet 2014 0.76
63 Update on the 22q11.2 deletion syndrome and its relevance to schizophrenia. Curr Opin Psychiatry 2017 0.76
64 Sibship characteristics in a familial sample with genetic susceptibility to schizophrenia. Schizophr Res 2007 0.75
65 Re: Familial aggregation of clinical and neurocognitive features in sibling pairs with and without schizophrenia. Schizophr Res 2009 0.75