Skip to Main Content

Author Details

Anne S Bassett
Institute of Medical Science, University of Toronto
1986
324
69
PMIDPaper TitleJournal TitlePublished Year
37717890Prenatal vs postnatal diagnosis of 22q11.2 deletion syndrome: cardiac and noncardiac outcomes through 1 year of age.Am J Obstet Gynecol2024
36380236Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia.Mol Psychiatry2023
37996907Correction: Polygenic risk for triglyceride levels in the presence of a high impact rare variant.BMC Med Genomics2023
37940981Polygenic risk for triglyceride levels in the presence of a high impact rare variant.BMC Med Genomics2023
35748435Elevated regional cerebral blood flow in adults with 22q11.2 deletion syndrome.World J Biol Psychiatry2023
37419092Approaches to studying the impact of 22q11.2 copy number variants.Am J Hum Genet2023
37449408An online survey to understand the needs of caregivers of family members with 22q11 deletion syndrome.J Intellect Disabil Res2023
36889031Adult-onset obstructive sleep apnea and pediatric pharyngoplasty in 22q11.2 deletion syndrome.Sleep Med2023
36463725Clinical genetics of schizophrenia and related neuropsychiatric disorders.Psychiatry Res2023
36869225Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia.Mol Psychiatry2023
36672911Gathering the Stakeholder's Perspective: Experiences and Opportunities in Rare Genetic Disease Research.Genes (Basel)2023
36672900Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions.Genes (Basel)2023
36729053Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome.Genet Med2023
36729052Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndrome.Genet Med2023
36075864Platelet findings in 22q11.2 deletion syndrome correlate with disease manifestations but do not correlate with GPIb surface expression.Clin Genet2023
33443009Within-family influences on dimensional neurobehavioral traits in a high-risk genetic model.Psychol Med2022
35546631Genome-wide tandem repeat expansions contribute to schizophrenia risk.Mol Psychiatry2022
35495153Schizophrenia Risk Mediated by microRNA Target Genes Overlapped by Genome-Wide Rare Copy Number Variation in 22q11.2 Deletion Syndrome.Front Genet2022
35521712Hypertriglyceridemia in young adults with a 22q11.2 microdeletion.Eur J Endocrinol2022
36421801Reproductive Outcomes in Adults with 22q11.2 Deletion Syndrome.Genes (Basel)2022
36002662Spectrum of movement disorders and motor abnormalities in adults with a 22q11.2 microdeletion: Comment on the literature and retrospective study of 92 adults.Eur J Hum Genet2022
36360275Adult Height, 22q11.2 Deletion Extent, and Short Stature in 22q11.2 Deletion Syndrome.Genes (Basel)2022
35899837Neurodevelopmental functioning in probands and non-proband carriers of 22q11.2 microduplication.Am J Med Genet A2022
36292685Influence of Parent-of-Origin on Intellectual Outcomes in the Chromosome 22q11.2 Deletion Syndrome.Genes (Basel)2022
33782512A normative chart for cognitive development in a genetically selected population.Neuropsychopharmacology2022
33615640Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA working groups on CNVs.Hum Brain Mapp2022
35191118The COVID-19 pandemic's impact on worry and medical disruptions reported by individuals with chromosome 22q11.2 copy number variants and their caregivers.J Intellect Disabil Res2022
34886679Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries.Circ Res2022
35063188A Regional Burden of Sequence-Level Variation in the 22q11.2 Region Influences Schizophrenia Risk and Educational Attainment.Biol Psychiatry2022
35304602Biallelic PAN2 variants in individuals with a syndromic neurodevelopmental disorder and multiple congenital anomalies.Eur J Hum Genet2022
35236119Genes To Mental Health (G2MH): A Framework to Map the Combined Effects of Rare and Common Variants on Dimensions of Cognition and Psychopathology.Am J Psychiatry2022
34291536Sexual knowledge and behaviour in 22q11.2 deletion syndrome, a complex care condition.J Appl Res Intellect Disabil2022
32772800Cognitive behavioral therapy in 22q11.2 deletion syndrome: A case study of two young adults with an anxiety disorder.J Intellect Disabil2021
33526774Genome sequencing broadens the range of contributing variants with clinical implications in schizophrenia.Transl Psychiatry2021
34588949Functional Activities Detected in the Olfactory Bulb and Associated Olfactory Regions in the Human Brain Using T2-Prepared BOLD Functional MRI at 7T.Front Neurosci2021
34404688Estimate of the contemporary live-birth prevalence of recurrent 22q11.2 deletions: a cross-sectional analysis from population-based newborn screening.CMAJ Open2021
34547032Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease.PLoS Genet2021
34328347Clinical Genetic Risk Variants Inform a Functional Protein Interaction Network for Tetralogy of Fallot.Circ Genom Precis Med2021
32015465Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion.Mol Psychiatry2021
31363180A genetic model for multimorbidity in young adults.Genet Med2020
32086293Erratum. Evaluation of the Genetic Association Between Adult Obesity and Neuropsychiatric Disease. Diabetes 2019;68:2235-2246.Diabetes2020
31870554Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects.Am J Hum Genet2020
31958577The role of 22q11.2 deletion syndrome in the relationship between congenital heart disease and scoliosis.Spine J2020
3308912522q11.2 microdeletion and increased risk for type 2 diabetes.EClinicalMedicine2020
33110418Genes and Pathways Implicated in Tetralogy of Fallot Revealed by Ultra-Rare Variant Burden Analysis in 231 Genome Sequences.Front Genet2020
32386091Age-Related Parkinsonian Signs in Microdeletion 22q11.2.Mov Disord2020
32407568Personalized medical information card for adults with 22q11.2 deletion syndrome: An initiative to improve communication between patients and healthcare providers.J Appl Res Intellect Disabil2020
32348848Impact of a 22q11.2 Microdeletion on Adult All-Cause Mortality in Tetralogy of Fallot Patients.Can J Cardiol2020
29895892Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size.Mol Psychiatry2020
30604657Low prevalence of substance use in people with 22q11.2 deletion syndrome.Br J Psychiatry2019
  • 1 - 50 of 324

Recommended Authors

Catherine A Brownstein
Harvard Medical School.
Career Start Year 2008
Number of shared co-authors 9
Lea K Davis
Vanderbilt University Medical Center, Tennessee Vanderbilt Genetics Institute
Career Start Year 2008
Number of shared co-authors 24
Stephan Ripke
Massachusetts General Hospital and Harvard Medical School
Career Start Year 2007
Number of shared co-authors 62
Douglas M Ruderfer
Vanderbilt University Medical Center
Career Start Year 2006
Number of shared co-authors 55
Per Hoffmann
Institute of Human Genetics, University of Bonn and University Hospital Bonn
Career Start Year 2005
Number of shared co-authors 65
Manuel Mattheisen
Dalhousie University
Career Start Year 2005
Number of shared co-authors 68
Sarah E Bergen
Karolinska Institutet
Career Start Year 2004
Number of shared co-authors 59
Anna C Need
Imperial College London
Career Start Year 2003
Number of shared co-authors 22
Tiffany A Greenwood
University of California San Diego
Career Start Year 2001
Number of shared co-authors 47
Anjene Addington
National Institute of Mental Health in Bethesda
Career Start Year 2001
Number of shared co-authors 17
Stefan Herms
Institute of Human Genetics, University of Bonn
Career Start Year 2001
Number of shared co-authors 60
Stephanie Le Hellard
University of Bergen
Career Start Year 1999
Number of shared co-authors 38
Janice M Fullerton
University of New South Wales
Career Start Year 1999
Number of shared co-authors 51
Thomas G Schulze
SUNY Upstate Medical University
Career Start Year 1998
Number of shared co-authors 59
Shaun Purcell
Brigham and Women's Hospital
Career Start Year 1998
Number of shared co-authors 64
Matthew W State
UCSF Weill Institute for Neurosciences, University of California san francisco
Career Start Year 1997
Number of shared co-authors 48
Dalila Pinto
Icahn School of Medicine at Mount Sinai
Career Start Year 1997
Number of shared co-authors 52
Zoran Brkanac
University of Washington
Career Start Year 1996
Number of shared co-authors 6
Marcella Rietschel
Central Institute of Mental Health, University of Mannheim
Career Start Year 1990
Number of shared co-authors 72
Daniel H Geschwind
University of California los angeles
Career Start Year 1989
Number of shared co-authors 62
Pak C Sham
the University of Hong Kong
Career Start Year 1989
Number of shared co-authors 36
Markus M N??then
Institute of Human Genetics, University Hospital Bonn
Career Start Year 1989
Number of shared co-authors 77
Laura M Kasch
Johns Hopkins School of Medicine
Career Start Year 1989
Number of shared co-authors 3
Bertram M??ller-Myhsok
Max Planck Institute of Psychiatry
Career Start Year 1989
Number of shared co-authors 69
Tatiana Foroud
Indiana University School of Medicine
Career Start Year 1988
Number of shared co-authors 73
Susan L Santangelo
Maine Medical Center Research Institute
Career Start Year 1986
Number of shared co-authors 44
Joachim Hallmayer
Stanford University School of Medicine
Career Start Year 1985
Number of shared co-authors 41
Judith A Badner
Rush University Medical College
Career Start Year 1984
Number of shared co-authors 43
Frances Lucy Raymond
University of Cambridge, UK Cambridge University Hospitals NHS Foundation Trust
Career Start Year 1983
Number of shared co-authors 11
Stephen J Glatt
SUNY Upstate Medical University
Career Start Year 1981
Number of shared co-authors 30

Collaborators

Linda M Brzustowicz
The State University of New Jersey
Co-authored papers 31
Christian R Marshall
Co-authored papers 29
Stephen W Scherer
The Hospital for Sick Children
Co-authored papers 29
Nancy J Butcher
The Hospital for Sick Children Research Institute
Co-authored papers 25
Elaine H Zackai
Children's Hospital of Philadelphia
Co-authored papers 18
Michael J Owen
Co-authored papers 15
Gabriela M Repetto
Clinica Alemana Universidad del Desarrollo
Co-authored papers 14
Raquel E Gur
University of Pennsylvania Perelman School of Medicine
Co-authored papers 13
Rodney C P Go
University of Alabama at Birmingham.
Co-authored papers 13
Dimitrios Avramopoulos
Johns Hopkins School of Medicine
Co-authored papers 13
Maria Cristina Digilio
Co-authored papers 11
James L Kennedy
Institute of Medical Sciences, University of Toronto
Co-authored papers 11
Margaret Daniele Fallin
Co-authored papers 11
Ryan K C Yuen
Co-authored papers 9
Rodney T Perry
University of Alabama at Birmingham.
Co-authored papers 9
Brian Caffo
Co-authored papers 9
Marilyn Albert
Johns Hopkins University School of Medicine
Co-authored papers 8
Rudolph E Tanzi
Co-authored papers 8
Elizabeth Goldmuntz
Co-authored papers 7
Vandana Shashi
Duke University School of Medicine
Co-authored papers 6
Lindy E Harrell
University of Alabama at Birmingham
Co-authored papers 6
Michael C O'Donovan
Co-authored papers 6
Peter C M van Zijl
Johns Hopkins University School of Medicine
Co-authored papers 6
Stephen R Hooper
University of North Carolina-Chapel Hill
Co-authored papers 5
Veronica J Vieland
The Ohio State University
Co-authored papers 5
Bruno Dallapiccola
Co-authored papers 5
Jason Brandt
The Johns Hopkins University School of Medicine
Co-authored papers 4
Peter Szatmari
Hospital for Sick Children, University of Toronto
Co-authored papers 4
Jared E Hayter
Co-authored papers 4
Mehdi Zarrei
Co-authored papers 4
Release 1.2