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Anne S. Bassett, M.D. - Publications

Affiliations: 
University of Toronto, Toronto, ON, Canada 
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Year Citation  Score
2024 Ge R, Ching CRK, Bassett AS, Kushan L, Antshel KM, van Amelsvoort T, Bakker G, Butcher NJ, Campbell LE, Chow EWC, Craig M, Crossley NA, Cunningham A, Daly E, Doherty JL, et al. Source-based morphometry reveals structural brain pattern abnormalities in 22q11.2 deletion syndrome. Human Brain Mapping. 45: e26553. PMID 38224541 DOI: 10.1002/hbm.26553  0.617
2023 Gur R, Bearden C, Jacquemont S, Jizi K, van TA, van den Bree M, Vorstman J, Sebat J, Ruparel K, Gallagher R, Swillen A, McClellan E, White L, Crowley T, Giunta V, ... ... Bassett A, et al. Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research Square. PMID 38234766 DOI: 10.21203/rs.3.rs-3393845/v1  0.36
2023 Freud LR, Galloway S, Crowley TB, Moldenhauer J, Swillen A, Breckpot J, Borrell A, Vora NL, Cuneo B, Hoffman H, Gilbert L, Nowakowska B, Geremek M, Kutkowska-Kaźmierczak A, Vermeesch JR, ... ... Bassett A, et al. Prenatal versus Postnatal Diagnosis of 22q11.2 Deletion Syndrome: Cardiac and Non-Cardiac Outcomes through 1 Year of Age. American Journal of Obstetrics and Gynecology. PMID 37717890 DOI: 10.1016/j.ajog.2023.09.005  0.306
2023 Zhao Y, Wang Y, Shi L, McDonald-McGinn DM, Crowley TB, McGinn DE, Tran OT, Miller D, Lin JR, Zackai E, Johnston HR, Chow EWC, Vorstman JAS, Vingerhoets C, van Amelsvoort T, ... ... Bassett AS, et al. Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS. Npj Genomic Medicine. 8: 17. PMID 37463940 DOI: 10.1038/s41525-023-00363-y  0.325
2023 Bassett AS, McDonald-McGinn DM, Boot E, Óskarsdóttir S, Yuen RKC. Approaches to studying the impact of 22q11.2 copy number variants. American Journal of Human Genetics. 110: 1216-1218. PMID 37419092 DOI: 10.1016/j.ajhg.2023.05.008  0.306
2023 Lin JR, Zhao Y, Jabalameli MR, Nguyen N, Mitra J, Swillen A, Vorstman JAS, Chow EWC, van den Bree M, Emanuel BS, Vermeesch JR, Owen MJ, Williams NM, Bassett AS, McDonald-McGinn DM, et al. Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia. Molecular Psychiatry. PMID 36869225 DOI: 10.1038/s41380-023-02009-y  0.47
2023 Óskarsdóttir S, Boot E, Crowley TB, Loo JCY, Arganbright JM, Armando M, Baylis AL, Breetvelt EJ, Castelein RM, Chadehumbe M, Cielo CM, de Reuver S, Eliez S, Fiksinski AM, Forbes BJ, ... ... Bassett AS, et al. Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 100338. PMID 36729053 DOI: 10.1016/j.gim.2022.11.006  0.329
2023 Boot E, Óskarsdóttir S, Loo JCY, Crowley TB, Orchanian-Cheff A, Andrade DM, Arganbright JM, Castelein RM, Cserti-Gazdewich C, de Reuver S, Fiksinski AM, Klingberg G, Lang AE, Mascarenhas MR, Moss EM, ... ... Bassett AS, et al. Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndrome. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 100344. PMID 36729052 DOI: 10.1016/j.gim.2022.11.012  0.32
2023 Blagowidow N, Nowakowska B, Schindewolf E, Grati FR, Putotto C, Breckpot J, Swillen A, Crowley TB, Loo JCY, Lairson LA, Óskarsdóttir S, Boot E, Garcia-Minaur S, Cristina Digilio M, Marino B, ... ... Bassett AS, et al. Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions. Genes. 14. PMID 36672900 DOI: 10.3390/genes14010160  0.343
2022 Bassett AS. Clinical genetics of schizophrenia and related neuropsychiatric disorders. Psychiatry Research. 319: 114992. PMID 36463725 DOI: 10.1016/j.psychres.2022.114992  0.426
2022 Palmer LD, McManus Z, Heung T, McAlpine G, Blagojevic C, Corral M, Bassett AS. Reproductive Outcomes in Adults with 22q11.2 Deletion Syndrome. Genes. 13. PMID 36421801 DOI: 10.3390/genes13112126  0.322
2022 Wen J, Trost B, Engchuan W, Halvorsen M, Pallotto LM, Mitina A, Ancalade N, Farrell M, Backstrom I, Guo K, Pellecchia G, Thiruvahindrapuram B, Giusti-Rodriguez P, Rosen JD, Li Y, ... ... Bassett AS, et al. Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia. Molecular Psychiatry. PMID 36380236 DOI: 10.1038/s41380-022-01857-4  0.367
2022 Heung T, Conroy B, Malecki S, Ha J, Boot E, Corral M, Bassett AS. Adult Height, 22q11.2 Deletion Extent, and Short Stature in 22q11.2 Deletion Syndrome. Genes. 13. PMID 36360275 DOI: 10.3390/genes13112038  0.392
2022 McGinn DE, Crowley TB, Heung T, Tran O, Moss E, Zackai EH, Emanuel BS, Chow EWC, Morrow BE, Swillen A, Bassett AS, McDonald-McGinn DM. Influence of Parent-of-Origin on Intellectual Outcomes in the Chromosome 22q11.2 Deletion Syndrome. Genes. 13. PMID 36292685 DOI: 10.3390/genes13101800  0.311
2022 Campbell IM, Crowley TB, Jobaliya C, Bailey A, McGinn DE, Gaiser K, Bassett A, Gur RE, Morrow B, Emanuel BS, Franco AT, French D, Zackai EH, McDonald-McGinn DM, Lambert MP. Platelet findings in 22q11.2 deletion syndrome correlate with disease manifestations but do not correlate with GPIb surface expression. Clinical Genetics. PMID 36075864 DOI: 10.1111/cge.14227  0.356
2022 Drmic IE, MacKinnon Modi B, McConnell B, Jilderda S, Hoang N, Noor A, Bassett AS, Speevak M, Stavropoulos DJ, Carter MT. Neurodevelopmental functioning in probands and non-proband carriers of 22q11.2 microduplication. American Journal of Medical Genetics. Part A. PMID 35899837 DOI: 10.1002/ajmg.a.62916  0.401
2022 Pasternak M, Shirzadi Z, Mutsaerts HJ, Boot E, Butcher NJ, MacIntosh BJ, Heung T, Bassett AS, Masellis M. Elevated regional cerebral blood flow in adults with 22q11.2 deletion syndrome. The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry. 1-15. PMID 35748435 DOI: 10.1080/15622975.2022.2093969  0.664
2022 Mojarad BA, Engchuan W, Trost B, Backstrom I, Yin Y, Thiruvahindrapuram B, Pallotto L, Mitina A, Khan M, Pellecchia G, Haque B, Guo K, Heung T, Costain G, Scherer SW, ... ... Bassett AS, et al. Genome-wide tandem repeat expansions contribute to schizophrenia risk. Molecular Psychiatry. PMID 35546631 DOI: 10.1038/s41380-022-01575-x  0.386
2022 Ying S, Heung T, Zhang Z, Yuen RKC, Bassett AS. Schizophrenia Risk Mediated by microRNA Target Genes Overlapped by Genome-Wide Rare Copy Number Variation in 22q11.2 Deletion Syndrome. Frontiers in Genetics. 13: 812183. PMID 35495153 DOI: 10.3389/fgene.2022.812183  0.347
2021 Breetvelt EJ, Smit KC, van Setten J, Merico D, Wang X, Vaartjes I, Bassett AS, Boks MPM, Szatmari P, Scherer SW, Kahn RS, Vorstman JAS. A Regional Burden of Sequence-Level Variation in the 22q11.2 Region Influences Schizophrenia Risk and Educational Attainment. Biological Psychiatry. PMID 35063188 DOI: 10.1016/j.biopsych.2021.11.019  0.335
2021 Sønderby IE, Ching CRK, Thomopoulos SI, van der Meer D, Sun D, Villalon-Reina JE, Agartz I, Amunts K, Arango C, Armstrong NJ, Ayesa-Arriola R, Bakker G, Bassett AS, Boomsma DI, Bülow R, et al. Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA working groups on CNVs. Human Brain Mapping. PMID 33615640 DOI: 10.1002/hbm.25354  0.663
2021 Mojarad BA, Yin Y, Manshaei R, Backstrom I, Costain G, Heung T, Merico D, Marshall CR, Bassett AS, Yuen RKC. Genome sequencing broadens the range of contributing variants with clinical implications in schizophrenia. Translational Psychiatry. 11: 84. PMID 33526774 DOI: 10.1038/s41398-021-01211-2  0.391
2021 Fiksinski AM, Heung T, Corral M, Breetvelt EJ, Costain G, Marshall CR, Kahn RS, Vorstman JAS, Bassett AS. Within-family influences on dimensional neurobehavioral traits in a high-risk genetic model. Psychological Medicine. 1-9. PMID 33443009 DOI: 10.1017/S0033291720005279  0.309
2020 Davies RW, Fiksinski AM, Breetvelt EJ, Williams NM, Hooper SR, Monfeuga T, Bassett AS, Owen MJ, Gur RE, Morrow BE, McDonald-McGinn DM, Swillen A, Chow EWC, van den Bree M, Emanuel BS, et al. Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome. Nature Medicine. PMID 33169016 DOI: 10.1038/s41591-020-1103-1  0.431
2020 Van L, Heung T, Malecki SL, Fenn C, Tyrer A, Sanches M, Chow EWC, Boot E, Corral M, Dash S, George SR, Bassett AS. 22q11.2 microdeletion and increased risk for type 2 diabetes. Eclinicalmedicine. 26: 100528. PMID 33089125 DOI: 10.1016/J.Eclinm.2020.100528  0.468
2020 Buijs PC, Bassett AS, Gold DA, Boot E. Cognitive behavioral therapy in 22q11.2 deletion syndrome: A case study of two young adults with an anxiety disorder. Journal of Intellectual Disabilities : Joid. 1744629520942374. PMID 32772800 DOI: 10.1177/1744629520942374  0.421
2020 Loo JCY, Boot E, Corral M, Bassett AS. Personalized medical information card for adults with 22q11.2 deletion syndrome: An initiative to improve communication between patients and healthcare providers. Journal of Applied Research in Intellectual Disabilities : Jarid. PMID 32407568 DOI: 10.1111/Jar.12747  0.354
2020 Boot E, Mentzel TQ, Palmer LD, van Harten PN, Marras C, Lang AE, Bassett AS. Age-Related Parkinsonian Signs in Microdeletion 22q11.2. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 32386091 DOI: 10.1002/Mds.28080  0.486
2020 van Mil S, Heung T, Malecki S, Van L, Chang J, Breetvelt E, Wald R, Oechslin E, Silversides C, Bassett AS. Impact of a 22q11.2 microdeletion on adult all-cause mortality in tetralogy of Fallot. The Canadian Journal of Cardiology. PMID 32348848 DOI: 10.1016/J.Cjca.2020.04.019  0.453
2020 Ching CRK, Gutman BA, Sun D, Villalon Reina J, Ragothaman A, Isaev D, Zavaliangos-Petropulu A, Lin A, Jonas RK, Kushan L, Pacheco-Hansen L, Vajdi A, Forsyth JK, Jalbrzikowski M, Bakker G, ... ... Bassett AS, et al. Mapping Subcortical Brain Alterations in 22q11.2 Deletion Syndrome: Effects of Deletion Size and Convergence With Idiopathic Neuropsychiatric Illness. The American Journal of Psychiatry. appiajp201919060583. PMID 32046535 DOI: 10.1176/Appi.Ajp.2019.19060583  0.708
2020 Cleynen I, Engchuan W, Hestand MS, Heung T, Holleman AM, Johnston HR, Monfeuga T, McDonald-McGinn DM, Gur RE, Morrow BE, Swillen A, Vorstman JAS, Bearden CE, Chow EWC, van den Bree M, ... ... Bassett AS, et al. Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion. Molecular Psychiatry. PMID 32015465 DOI: 10.1038/S41380-020-0654-3  0.757
2020 Homans JF, de Reuver S, Heung T, Silversides CK, Oechslin EN, Houben ML, McDonald-McGinn DM, Kruyt MC, Castelein RM, Bassett AS. The Role of 22q11.2 Deletion Syndrome in the Relationship between Congenital Heart Disease and Scoliosis. The Spine Journal : Official Journal of the North American Spine Society. PMID 31958577 DOI: 10.1016/J.Spinee.2020.01.006  0.475
2019 Vervoort L, Demaerel W, Rengifo LY, Odrzywolski A, Vergaelen E, Hestand MS, Breckpot J, Devriendt K, Swillen A, McDonald-McGinn DM, Fiksinski AM, Zinkstok JR, Morrow BE, Heung T, Vorstman JAS, ... Bassett AS, et al. Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic origins. Human Molecular Genetics. 28: 3724-3733. PMID 31884517 DOI: 10.1093/Hmg/Ddz166  0.462
2019 Zhao Y, Diacou A, Johnston HR, Musfee FI, McDonald-McGinn DM, McGinn D, Crowley TB, Repetto GM, Swillen A, Breckpot J, Vermeesch JR, Kates WR, Digilio MC, Unolt M, Marino B, ... ... Bassett AS, et al. Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects. American Journal of Human Genetics. PMID 31870554 DOI: 10.1016/J.Ajhg.2019.11.010  0.471
2019 Zarrei M, Burton CL, Engchuan W, Young EJ, Higginbotham EJ, MacDonald JR, Trost B, Chan AJS, Walker S, Lamoureux S, Heung T, Mojarad BA, Kellam B, Paton T, Faheem M, ... ... Bassett AS, et al. A large data resource of genomic copy number variation across neurodevelopmental disorders. Npj Genomic Medicine. 4: 26. PMID 31602316 DOI: 10.1038/S41525-019-0098-3  0.348
2019 Zinkstok JR, Boot E, Bassett AS, Hiroi N, Butcher NJ, Vingerhoets C, Vorstman JAS, van Amelsvoort TAMJ. Neurobiological perspective of 22q11.2 deletion syndrome. The Lancet. Psychiatry. PMID 31395526 DOI: 10.1016/S2215-0366(19)30076-8  0.728
2019 Malecki SL, Van Mil S, Graffi J, Breetvelt E, Corral M, Boot E, Chow EWC, Sanches M, Verma AA, Bassett AS. A genetic model for multimorbidity in young adults. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 31363180 DOI: 10.1038/S41436-019-0603-1  0.426
2019 Van L, Heung T, Graffi J, Ng E, Malecki S, Van Mil S, Boot E, Corral M, Chow EWC, Hodgkinson KA, Silversides C, Bassett AS. All-cause mortality and survival in adults with 22q11.2 deletion syndrome. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 30948858 DOI: 10.1038/S41436-019-0509-Y  0.451
2019 Vlaskamp DRM, Bassett AS, Sullivan JE, Robblee J, Sadleir LG, Scheffer IE, Andrade DM. Schizophrenia is a later-onset feature of PCDH19 Girls Clustering Epilepsy. Epilepsia. 60: 429-440. PMID 30828795 DOI: 10.1111/Epi.14678  0.375
2019 Boot E, Bassett AS, Marras C. 22q11.2 Deletion Syndrome-Associated Parkinson's Disease. Movement Disorders Clinical Practice. 6: 11-16. PMID 30746410 DOI: 10.1002/Mdc3.12687  0.462
2019 Costain G, Walker S, Argiropoulos B, Baribeau DA, Bassett AS, Boot E, Devriendt K, Kellam B, Marshall CR, Prasad A, Serrano MA, Stavropoulos DJ, Twede H, Vermeesch JR, Vorstman JAS, et al. Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders. Journal of Neurodevelopmental Disorders. 11: 3. PMID 30732576 DOI: 10.1186/S11689-019-9263-3  0.349
2019 Vingerhoets C, van Oudenaren MJF, Bloemen OJN, Boot E, van Duin EDA, Evers LJM, Fiksinski AM, Breetvelt EJ, Palmer LD, Vergaelen E, Vogels A, Meijer C, Booij J, de Haan L, ... ... Bassett AS, et al. Low prevalence of substance use in people with 22q11.2 deletion syndrome. The British Journal of Psychiatry : the Journal of Mental Science. 1-7. PMID 30604657 DOI: 10.1192/Bjp.2018.258  0.492
2019 Monfeuga T, Epstein MP, Holleman AM, Cleynen I, Johnston H, Zhao Y, McDonald-McGinn DM, Gur RE, Warren ST, Vermeesch J, Emanuel BS, Morrow BE, Bassett AS, Williams N. 7Schizophrenia Polygenic Risk Score Analysis In 22Q11.2 Deletion Syndrome European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2018.08.014  0.56
2018 Rezazadeh A, Bercovici E, Kiehl TR, Chow EW, Krings T, Bassett AS, Andrade DM. Periventricular nodular heterotopia in 22q11.2 deletion and frontal lobe migration. Annals of Clinical and Translational Neurology. 5: 1314-1322. PMID 30480026 DOI: 10.1002/Acn3.641  0.499
2018 Zhao Y, Guo T, Fiksinski A, Breetvelt E, McDonald-McGinn DM, Crowley TB, Diacou A, Schneider M, Eliez S, Swillen A, Breckpot J, Vermeesch J, Chow EWC, Gothelf D, Duijff S, ... ... Bassett AS, et al. Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects. American Journal of Medical Genetics. Part A. PMID 30289625 DOI: 10.1002/Ajmg.A.40359  0.434
2018 Sumitomo A, Horike K, Hirai K, Butcher N, Boot E, Sakurai T, Nucifora FC, Bassett AS, Sawa A, Tomoda T. A mouse model of 22q11.2 deletions: Molecular and behavioral signatures of Parkinson's disease and schizophrenia. Science Advances. 4: eaar6637. PMID 30116778 DOI: 10.1126/Sciadv.Aar6637  0.7
2018 Fiksinski AM, Breetvelt EJ, Lee YJ, Boot E, Butcher N, Palmer L, Chow EWC, Kahn RS, Vorstman JAS, Bassett AS. Neurocognition and adaptive functioning in a genetic high risk model of schizophrenia. Psychological Medicine. 1-8. PMID 30064532 DOI: 10.1017/S0033291718001824  0.703
2018 Sun D, Ching CRK, Lin A, Forsyth JK, Kushan L, Vajdi A, Jalbrzikowski M, Hansen L, Villalon-Reina JE, Qu X, Jonas RK, van Amelsvoort T, Bakker G, Kates WR, Antshel KM, ... ... Bassett AS, et al. Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size. Molecular Psychiatry. PMID 29895892 DOI: 10.1038/S41380-018-0078-5  0.706
2018 Butcher NJ, Boot E, Lang AE, Andrade D, Vorstman J, McDonald-McGinn D, Bassett AS. Neuropsychiatric expression and catatonia in 22q11.2 deletion syndrome: An overview and case series. American Journal of Medical Genetics. Part A. PMID 29777584 DOI: 10.1002/Ajmg.A.38708  0.732
2018 Boot E, Butcher NJ, Udow S, Marras C, Mok KY, Kaneko S, Barrett MJ, Prontera P, Berman BD, Masellis M, Dufournet B, Nguyen K, Charles P, Mutez E, Danaila T, ... ... Bassett AS, et al. Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2. Neurology. PMID 29752303 DOI: 10.1212/Wnl.0000000000005660  0.621
2018 Palmer LD, Butcher NJ, Boot E, Hodgkinson KA, Heung T, Chow EWC, Guna A, Crowley TB, Zackai E, McDonald-McGinn DM, Bassett AS. Elucidating the diagnostic odyssey of 22q11.2 deletion syndrome. American Journal of Medical Genetics. Part A. 176: 936-944. PMID 29575622 DOI: 10.1002/Ajmg.A.38645  0.674
2018 Manley W, Moreau MP, Azaro M, Siecinski SK, Davis G, Buyske S, Vieland V, Bassett AS, Brzustowicz L. Validation of a microRNA target site polymorphism in H3F3B that is potentially associated with a broad schizophrenia phenotype. Plos One. 13: e0194233. PMID 29529098 DOI: 10.1371/Journal.Pone.0194233  0.424
2018 Unolt M, Barry J, Digilio MC, Marino B, Bassett A, Oechslin E, Low DW, Belasco JB, Kallish S, Sullivan K, Zackai EH, McDonald-McGinn DM. Primary lymphedema and other lymphatic anomalies are associated with 22q11.2 deletion syndrome. European Journal of Medical Genetics. PMID 29447908 DOI: 10.1016/J.Ejmg.2018.02.006  0.466
2018 Buijs PCM, Bassett AS, Boot E. Non-pharmacological treatment of psychiatric disorders in individuals with 22q11.2 deletion syndrome; a systematic review. American Journal of Medical Genetics. Part A. PMID 29363845 DOI: 10.1002/Ajmg.A.38612  0.404
2018 Guo T, Diacou A, Hiroko N, McDonald-McGinn DM, Hestand M, Demaerel W, Zhang L, Zhao Y, Ujueta F, Shan J, Montagna C, Zheng D, Crowley TB, Kushan-Wells L, Bearden CE, ... ... Bassett AS, et al. Deletion size analysis of 1,680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2. Human Molecular Genetics. PMID 29361080 DOI: 10.1093/Hmg/Ddy028  0.477
2018 Ania F, Vorstman J, Bassett A, Breetvelt E. S132. A NORMATIVE CHART FOR THE TRAJECTORY OF COGNITIVE FUNCTIONING IN INDIVIDUALS AT HIGH RISK FOR SCHIZOPHRENIA: LONGITUDINAL FINDINGS FROM THE INTERNATIONAL BRAIN AND BEHAVIOR CONSORTIUM ON 22Q11.2 DELETION SYNDROME Schizophrenia Bulletin. 44: S376-S377. DOI: 10.1093/Schbul/Sby018.919  0.489
2018 Ania F, Breetvelt E, Vorstman J, Chow E, Lee E, Palmer L, Boot E, Butcher N, Kahn R, Bassett A. F72. NEUROCOGNITION AND ADAPTIVE FUNCTIONING IN THE 22Q11.2 DELETION SYNDROME MODEL OF SCHIZOPHRENIA Schizophrenia Bulletin. 44: S247-S247. DOI: 10.1093/schbul/sby017.603  0.687
2018 Fiksinski A, Breetvelt E, Vorstman J, Lee E, Boot E, Butcher N, Palmer L, Chow E, Kahn R, Bassett A. F207. Neurocognition and Adaptive Functioning in the 22q11.2 Deletion Syndrome Model of Schizophrenia Biological Psychiatry. 83: S319. DOI: 10.1016/J.Biopsych.2018.02.821  0.713
2018 Fiksinski A, Vorstman J, Bassett A, Breetvelt E. S210. A Normative Chart for the Trajectory of Cognitive Functioning in a Genetically Selected Population: Longitudinal Findings From the International Brain and Behavior Consortium on 22q11.2 Deletion Syndrome Biological Psychiatry. 83: S429. DOI: 10.1016/J.Biopsych.2018.02.1102  0.397
2017 Lowther C, Merico D, Costain G, Waserman J, Boyd K, Noor A, Speevak M, Stavropoulos DJ, Wei J, Lionel AC, Marshall CR, Scherer SW, Bassett AS. Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophrenia. Genome Medicine. 9: 105. PMID 29187259 DOI: 10.1186/S13073-017-0488-Z  0.495
2017 Guo T, Repetto GM, McDonald McGinn DM, Chung JH, Nomaru H, Campbell CL, Blonska A, Bassett AS, Chow EWC, Mlynarski EE, Swillen A, Vermeesch J, Devriendt K, Gothelf D, Carmel M, et al. Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3. Circulation. Cardiovascular Genetics. 10. PMID 29025761 DOI: 10.1161/Circgenetics.116.001690  0.376
2017 Borlot F, Regan BM, Bassett AS, Stavropoulos DJ, Andrade DM. Prevalence of Pathogenic Copy Number Variation in Adults With Pediatric-Onset Epilepsy and Intellectual Disability. Jama Neurology. PMID 28846756 DOI: 10.1001/Jamaneurol.2017.1775  0.308
2017 Gur RE, Bassett AS, McDonald-McGinn DM, Bearden CE, Chow E, Emanuel BS, Owen M, Swillen A, Van den Bree M, Vermeesch J, Vorstman JAS, Warren S, Lehner T, Morrow B. A neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11.2 Deletion Syndrome Brain Behavior Consortium. Molecular Psychiatry. PMID 28761081 DOI: 10.1038/Mp.2017.161  0.543
2017 Bassett AS, Lowther C, Merico D, Costain G, Chow EWC, van Amelsvoort T, McDonald-McGinn D, Gur RE, Swillen A, Van den Bree M, Murphy K, Gothelf D, Bearden CE, Eliez S, Kates W, et al. Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome. The American Journal of Psychiatry. appiajp201716121417. PMID 28750581 DOI: 10.1176/Appi.Ajp.2017.16121417  0.596
2017 Bassett AS, Scherer SW. Copy Number Variation in Tourette Syndrome. Neuron. 94: 1041-1043. PMID 28641101 DOI: 10.1016/J.Neuron.2017.06.017  0.307
2017 Wither RG, Borlot F, MacDonald A, Butcher NJ, Chow EWC, Bassett AS, Andrade DM. 22q11.2 deletion syndrome lowers seizure threshold in adult patients without epilepsy. Epilepsia. PMID 28448680 DOI: 10.1111/Epi.13748  0.648
2017 Butcher NJ, Merico D, Zarrei M, Ogura L, Marshall CR, Chow EWC, Lang AE, Scherer SW, Bassett AS. Whole-genome sequencing suggests mechanisms for 22q11.2 deletion-associated Parkinson's disease. Plos One. 12: e0173944. PMID 28430790 DOI: 10.1371/Journal.Pone.0173944  0.639
2017 Butcher NJ, Marras C, Pondal M, Rusjan P, Boot E, Christopher L, Repetto GM, Fritsch R, Chow EW, Masellis M, Strafella AP, Lang AE, Bassett AS. Neuroimaging and clinical features in adults with a 22q11.2 deletion at risk of Parkinson's disease. Brain : a Journal of Neurology. PMID 28369257 DOI: 10.1093/Brain/Awx053  0.689
2017 Van L, Boot E, Bassett AS. Update on the 22q11.2 deletion syndrome and its relevance to schizophrenia. Current Opinion in Psychiatry. PMID 28230630 DOI: 10.1097/Yco.0000000000000324  0.588
2017 Fiksinski AM, Breetvelt EJ, Duijff SN, Bassett AS, Kahn RS, Vorstman JA. Autism Spectrum and psychosis risk in the 22q11.2 deletion syndrome. Findings from a prospective longitudinal study. Schizophrenia Research. PMID 28119035 DOI: 10.1016/J.Schres.2017.01.032  0.519
2017 Baharnoori M, Mandell DM, Andrade DM, Chow EWC, Bassett AS, Kiehl T. Periventricular nodular heterotopia and bilateral intraventricular xanthogranulomas in 22q11.2 deletion syndrome Human Pathology: Case Reports. 9: 55-57. DOI: 10.1016/J.Ehpc.2016.09.003  0.537
2016 Mak CCY, Chow PC, Liu APY, Chan KYK, Chu YWY, Mok GTK, Leung GKC, Yeung KS, Chau AKT, Lowther C, Scherer SW, Marshall CR, Bassett AS, Chung BHY. De novo large rare copy-number variations contribute to conotruncal heart disease in Chinese patients. Npj Genomic Medicine. 1: 16033. PMID 29263819 DOI: 10.1038/Npjgenmed.2016.33  0.48
2016 Costain G, Silversides CK, Bassett AS. The importance of copy number variation in congenital heart disease. Npj Genomic Medicine. 1: 16031. PMID 28706735 DOI: 10.1038/Npjgenmed.2016.31  0.43
2016 Bassett AS, Costain G, Marshall CR. Neuropsychiatric aspects of 22q11.2 deletion syndrome: considerations in the prenatal setting. Prenatal Diagnosis. PMID 27718271 DOI: 10.1002/Pd.4935  0.528
2016 Voll SL, Boot E, Butcher NJ, Cooper S, Heung T, Chow EW, Silversides CK, Bassett AS. Obesity in adults with 22q11.2 deletion syndrome. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 27537705 DOI: 10.1038/Gim.2016.98  0.637
2016 Lowther C, Speevak M, Armour CM, Goh ES, Graham GE, Li C, Zeesman S, Nowaczyk MJ, Schultz LA, Morra A, Nicolson R, Bikangaga P, Samdup D, Zaazou M, Boyd K, ... ... Bassett AS, et al. Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 27195815 DOI: 10.1038/Gim.2016.54  0.333
2016 Isles AR, Ingason A, Lowther C, Walters J, Gawlick M, Stöber G, Rees E, Martin J, Little RB, Potter H, Georgieva L, Pizzo L, Ozaki N, Aleksic B, Kushima I, ... ... Bassett A, et al. Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders. Plos Genetics. 12: e1005993. PMID 27153221 DOI: 10.1371/Journal.Pgen.1005993  0.542
2016 Mlynarski EE, Xie M, Taylor D, Sheridan MB, Guo T, Racedo SE, McDonald-McGinn DM, Chow EW, Vorstman J, Swillen A, Devriendt K, Breckpot J, Digilio MC, Marino B, Dallapiccola B, ... ... Bassett AS, et al. Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome. Human Genetics. PMID 26742502 DOI: 10.1007/S00439-015-1623-9  0.439
2015 McDonald-McGinn DM, Sullivan KE, Marino B, Philip N, Swillen A, Vorstman JA, Zackai EH, Emanuel BS, Vermeesch JR, Morrow BE, Scambler PJ, Bassett AS. 22q11.2 deletion syndrome. Nature Reviews. Disease Primers. 1: 15071. PMID 27189754 DOI: 10.1038/nrdp.2015.71  0.396
2015 Costain G, Lionel AC, Ogura L, Marshall CR, Scherer SW, Silversides CK, Bassett AS. Genome-wide rare copy number variations contribute to genetic risk for transposition of the great arteries. International Journal of Cardiology. 204: 115-121. PMID 26655555 DOI: 10.1016/J.Ijcard.2015.11.127  0.306
2015 Costain G, Roche SL, Scherer SW, Silversides CK, Bassett AS. Rare copy number variations in an adult with transposition of the great arteries emphasize the importance of updated genetic assessments in syndromic congenital cardiac disease. International Journal of Cardiology. 203: 516-518. PMID 26551885 DOI: 10.1016/J.Ijcard.2015.10.216  0.329
2015 Gross SJ, Stosic M, McDonald-McGinn DM, Bassett AS, Norvez A, Dhamankar R, Kobara K, Kirkizlar E, Zimmermann B, Wayham N, Babiarz JE, Ryan A, Jinnett KN, Demko Z, Benn P. Clinical Experience with Single-Nucleotide Polymorphism-Based Noninvasive Prenatal Screening for 22q11.2 Deletion Syndrome. Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology. PMID 26396068 DOI: 10.1002/Uog.15754  0.41
2015 Merico D, Zarrei M, Costain G, Ogura L, Alipanahi B, Gazzellone MJ, Butcher NJ, Thiruvahindrapuram B, Nalpathamkalam T, Chow EW, Andrade DM, Frey BJ, Marshall CR, Scherer SW, Bassett AS. Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion Syndrome. G3 (Bethesda, Md.). 5: 2453-61. PMID 26384369 DOI: 10.1534/G3.115.021345  0.732
2015 Guna A, Butcher NJ, Bassett AS. Comparative mapping of the 22q11.2 deletion region and the potential of simple model organisms. Journal of Neurodevelopmental Disorders. 7: 18. PMID 26137170 DOI: 10.1186/S11689-015-9113-X  0.701
2015 Boot E, Butcher NJ, Vorstman JA, van Amelsvoort TA, A Fung WL, Bassett AS. Pharmacological Treatment of 22q11.2 Deletion Syndrome-related Psychoses. Pharmacopsychiatry. PMID 26091278 DOI: 10.1055/S-0035-1554645  0.697
2015 Van L, Butcher NJ, Costain G, Ogura L, Chow EW, Bassett AS. Fetal growth and gestational factors as predictors of schizophrenia in 22q11.2 deletion syndrome. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 26087175 DOI: 10.1038/Gim.2015.84  0.746
2015 Hashemi B, Bassett A, Chitayat D, Chong K, Feldman M, Flanagan J, Goobie S, Kawamura A, Lowther C, Prasad C, Siu V, So J, Tung S, Speevak M, Stavropoulos DJ, et al. Deletion of 15q11.2(BP1-BP2) region: Further evidence for lack of phenotypic specificity in a pediatric population. American Journal of Medical Genetics. Part A. PMID 25946043 DOI: 10.1002/Ajmg.A.37134  0.471
2015 Mlynarski EE, Sheridan MB, Xie M, Guo T, Racedo SE, McDonald-McGinn DM, Gai X, Chow EW, Vorstman J, Swillen A, Devriendt K, Breckpot J, Digilio MC, Marino B, Dallapiccola B, ... ... Bassett AS, et al. Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome. American Journal of Human Genetics. 96: 753-64. PMID 25892112 DOI: 10.1016/J.Ajhg.2015.03.007  0.424
2015 Butcher NJ, Fung WL, Fitzpatrick L, Guna A, Andrade DM, Lang AE, Chow EW, Bassett AS. Response to clozapine in a clinically identifiable subtype of schizophrenia. The British Journal of Psychiatry : the Journal of Mental Science. 206: 484-91. PMID 25745132 DOI: 10.1192/Bjp.Bp.114.151837  0.641
2015 Vorstman JA, Breetvelt EJ, Duijff SN, Eliez S, Schneider M, Jalbrzikowski M, Armando M, Vicari S, Shashi V, Hooper SR, Chow EW, Fung WL, Butcher NJ, Young DA, McDonald-McGinn DM, ... ... Bassett AS, et al. Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndrome. Jama Psychiatry. 72: 377-85. PMID 25715178 DOI: 10.1001/Jamapsychiatry.2014.2671  0.704
2015 Boot E, Butcher NJ, van Amelsvoort TA, Lang AE, Marras C, Pondal M, Andrade DM, Fung WL, Bassett AS. Movement disorders and other motor abnormalities in adults with 22q11.2 deletion syndrome. American Journal of Medical Genetics. Part A. 167: 639-45. PMID 25684639 DOI: 10.1002/Ajmg.A.36928  0.686
2015 Chan C, Costain G, Ogura L, Silversides CK, Chow EW, Bassett AS. Reproductive Health Issues for Adults with a Common Genomic Disorder: 22q11.2 Deletion Syndrome. Journal of Genetic Counseling. PMID 25579115 DOI: 10.1007/S10897-014-9811-7  0.47
2015 Fung WL, Butcher NJ, Costain G, Andrade DM, Boot E, Chow EW, Chung B, Cytrynbaum C, Faghfoury H, Fishman L, García-Miñaúr S, George S, Lang AE, Repetto G, Shugar A, ... ... Bassett AS, et al. Practical guidelines for managing adults with 22q11.2 deletion syndrome. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 25569435 DOI: 10.1038/Gim.2014.175  0.695
2015 Lowther C, Costain G, Stavropoulos DJ, Melvin R, Silversides CK, Andrade DM, So J, Faghfoury H, Lionel AC, Marshall CR, Scherer SW, Bassett AS. Delineating the 15q13.3 microdeletion phenotype: a case series and comprehensive review of the literature. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 17: 149-57. PMID 25077648 DOI: 10.1038/Gim.2014.83  0.556
2015 Warnica W, Merico D, Costain G, Alfred SE, Wei J, Marshall CR, Scherer SW, Bassett AS. Copy number variable microRNAs in schizophrenia and their neurodevelopmental gene targets. Biological Psychiatry. 77: 158-66. PMID 25034949 DOI: 10.1016/J.Biopsych.2014.05.011  0.428
2015 Carter M, MacKinnon B, Jilderda S, Falcon J, Swaroop P, Dale B, Noor A, Bassett AS, Stavropoulos DJ, Drmic I. MG-105 Delineating the phenotypes associated with the 15q11.2 BP1-BP2 deletion: Preliminary trends in psychometric evaluation Journal of Medical Genetics. 52: A2.3-A3. DOI: 10.1136/Jmedgenet-2015-103578.6  0.446
2015 Lowther C, Speevak M, Armour C, Goh E, Graham G, Li C, Zeesman S, Nowaczyk MJ, Schultz L, Morra A, Nicolson R, Rajguru M, Goobie S, Tarnopolsky MA, Prasad C, ... ... Bassett AS, et al. MG-123 Exonic and intronic NRXN1 deletions: Novel genotype-phenotype correlations Journal of Medical Genetics. 52: A9.1-A9. DOI: 10.1136/Jmedgenet-2015-103578.23  0.387
2014 Baker K, Costain G, Fung WL, Bassett AS. Chromosomal microarray analysis-a routine clinical genetic test for patients with schizophrenia. The Lancet. Psychiatry. 1: 329-31. PMID 26360988 DOI: 10.1016/S2215-0366(14)70308-6  0.491
2014 Merico D, Costain G, Butcher NJ, Warnica W, Ogura L, Alfred SE, Brzustowicz LM, Bassett AS. MicroRNA Dysregulation, Gene Networks, and Risk for Schizophrenia in 22q11.2 Deletion Syndrome. Frontiers in Neurology. 5: 238. PMID 25484875 DOI: 10.3389/Fneur.2014.00238  0.699
2014 Costain G, Lionel AC, Fu F, Stavropoulos DJ, Gazzellone MJ, Marshall CR, Scherer SW, Bassett AS. Adult neuropsychiatric expression and familial segregation of 2q13 duplications. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 165: 337-44. PMID 24807792 DOI: 10.1002/Ajmg.B.32236  0.555
2014 Cheung EN, George SR, Costain GA, Andrade DM, Chow EW, Silversides CK, Bassett AS. Prevalence of hypocalcaemia and its associated features in 22q11·2 deletion syndrome. Clinical Endocrinology. 81: 190-6. PMID 24735350 DOI: 10.1111/Cen.12466  0.473
2014 Lowther C, Costain G, Melvin R, Stavropoulos DJ, Lionel AC, Marshall CR, Scherer SW, Bassett AS. Adult expression of a 3q13.31 microdeletion. Molecular Cytogenetics. 7: 23. PMID 24650298 DOI: 10.1186/1755-8166-7-23  0.587
2014 Schneider M, Debbané M, Bassett AS, Chow EW, Fung WL, van den Bree M, Owen M, Murphy KC, Niarchou M, Kates WR, Antshel KM, Fremont W, McDonald-McGinn DM, Gur RE, Zackai EH, et al. 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. The American Journal of Psychiatry. 171: 627-39. PMID 24577245 DOI: 10.1176/Appi.Ajp.2013.13070864  0.436
2014 Chin-Yee NJ, Costain G, Swaby JA, Silversides CK, Bassett AS. Reproductive fitness and genetic transmission of tetralogy of Fallot in the molecular age. Circulation. Cardiovascular Genetics. 7: 102-9. PMID 24563425 DOI: 10.1161/Circgenetics.113.000328  0.308
2014 Costain G, Bassett AS. Individualizing recurrence risks for severe mental illness: epidemiologic and molecular genetic approaches. Schizophrenia Bulletin. 40: 21-3. PMID 24045037 DOI: 10.1093/Schbul/Sbt133  0.489
2014 Cheung EN, George SR, Andrade DM, Chow EW, Silversides CK, Bassett AS. Neonatal hypocalcemia, neonatal seizures, and intellectual disability in 22q11.2 deletion syndrome. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 16: 40-4. PMID 23765047 DOI: 10.1038/Gim.2013.71  0.418
2014 Costain G, Esplen MJ, Toner B, Scherer SW, Meschino WS, Hodgkinson KA, Bassett AS. Evaluating genetic counseling for individuals with schizophrenia in the molecular age. Schizophrenia Bulletin. 40: 78-87. PMID 23236078 DOI: 10.1093/Schbul/Sbs138  0.475
2014 Karas DJ, Costain G, Chow EW, Bassett AS. Perceived burden and neuropsychiatric morbidities in adults with 22q11.2 deletion syndrome. Journal of Intellectual Disability Research : Jidr. 58: 198-210. PMID 23106770 DOI: 10.1111/J.1365-2788.2012.01639.X  0.453
2014 Costain G, Esplen MJ, Toner B, Hodgkinson KA, Bassett AS. Evaluating genetic counseling for family members of individuals with schizophrenia in the molecular age. Schizophrenia Bulletin. 40: 88-99. PMID 23104866 DOI: 10.1093/Schbul/Sbs124  0.439
2014 Merico D, Costain G, Butcher N, Warnica W, Ogura L, Alfred SE, Brzustowicz L, Bassett AS. MicroRNA target genes and risk for schizophrenia in 22q11.2 deletion syndrome Frontiers in Neurology. 5. DOI: 10.3389/Fneur.2014.00221  0.725
2014 Bassett AS. 22Q11.2 DELETION SYNDROME AS A GENETIC MODEL FOR SCHIZOPHRENIA Schizophrenia Research. 153: S76. DOI: 10.1016/S0920-9964(14)70245-2  0.576
2013 Costain G, McDonald-McGinn DM, Bassett AS. Prenatal genetic testing with chromosomal microarray analysis identifies major risk variants for schizophrenia and other later-onset disorders. The American Journal of Psychiatry. 170: 1498. PMID 24306343 DOI: 10.1176/Appi.Ajp.2013.13070880  0.507
2013 Yuen T, Chow EW, Silversides CK, Bassett AS. Premorbid adjustment and schizophrenia in individuals with 22q11.2 deletion syndrome. Schizophrenia Research. 151: 221-5. PMID 24262682 DOI: 10.1016/J.Schres.2013.10.041  0.515
2013 Butcher NJ, Kiehl TR, Hazrati LN, Chow EW, Rogaeva E, Lang AE, Bassett AS. 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 Neurology. 70: 1359-66. PMID 24018986 DOI: 10.1001/Jamaneurol.2013.3646  0.653
2013 Andrade DM, Krings T, Chow EW, Kiehl TR, Bassett AS. Hippocampal malrotation is associated with chromosome 22q11.2 microdeletion. The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. 40: 652-6. PMID 23968937 DOI: 10.1017/S0317167100014876  0.366
2013 Costain G, Lionel AC, Merico D, Forsythe P, Russell K, Lowther C, Yuen T, Husted J, Stavropoulos DJ, Speevak M, Chow EW, Marshall CR, Scherer SW, Bassett AS. Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarrays. Human Molecular Genetics. 22: 4485-501. PMID 23813976 DOI: 10.1093/Hmg/Ddt297  0.481
2013 Delio M, Guo T, McDonald-McGinn DM, Zackai E, Herman S, Kaminetzky M, Higgins AM, Coleman K, Chow C, Jalbrzikowski M, Jarlbrzkowski M, Bearden CE, Bailey A, Vangkilde A, Olsen L, ... ... Bassett A, et al. Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes. American Journal of Human Genetics. 92: 439-47. PMID 23453669 DOI: 10.1016/j.ajhg.2013.01.018  0.474
2013 Lionel AC, Vaags AK, Sato D, Gazzellone MJ, Mitchell EB, Chen HY, Costain G, Walker S, Egger G, Thiruvahindrapuram B, Merico D, Prasad A, Anagnostou E, Fombonne E, Zwaigenbaum L, ... ... Bassett AS, et al. Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures. Human Molecular Genetics. 22: 2055-66. PMID 23393157 DOI: 10.1093/Hmg/Ddt056  0.439
2013 Costain G, Bassett AS. Incomplete knowledge of the clinical context as a barrier to interpreting incidental genetic research findings. The American Journal of Bioethics : Ajob. 13: 58-60. PMID 23391068 DOI: 10.1080/15265161.2012.754063  0.304
2013 Vorstman JA, Breetvelt EJ, Thode KI, Chow EW, Bassett AS. Expression of autism spectrum and schizophrenia in patients with a 22q11.2 deletion. Schizophrenia Research. 143: 55-9. PMID 23153825 DOI: 10.1016/J.Schres.2012.10.010  0.572
2013 Dolcetti A, Silversides CK, Marshall CR, Lionel AC, Stavropoulos DJ, Scherer SW, Bassett AS. 1q21.1 Microduplication expression in adults. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 15: 282-9. PMID 23018752 DOI: 10.1038/Gim.2012.129  0.542
2012 Brzustowicz LM, Bassett AS. miRNA-mediated risk for schizophrenia in 22q11.2 deletion syndrome. Frontiers in Genetics. 3: 291. PMID 23248646 DOI: 10.3389/Fgene.2012.00291  0.552
2012 Costain G, Bassett AS. Clinical applications of schizophrenia genetics: genetic diagnosis, risk, and counseling in the molecular era. The Application of Clinical Genetics. 5: 1-18. PMID 23144566 DOI: 10.2147/Tacg.S21953  0.509
2012 Herman SB, Guo T, McGinn DM, Blonska A, Shanske AL, Bassett AS, Chow EW, Bowser M, Sheridan M, Beemer F, Devriendt K, Swillen A, Breckpot J, Digilio MC, Marino B, et al. Overt cleft palate phenotype and TBX1 genotype correlations in velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients. American Journal of Medical Genetics. Part A. 158: 2781-7. PMID 23034814 DOI: 10.1002/Ajmg.A.35512  0.441
2012 Costain G, Bassett AS. The ever-evolving concept of clinical significance and the potential for sins of omission in genetic research. The American Journal of Bioethics : Ajob. 12: 22-4. PMID 22974025 DOI: 10.1080/15265161.2012.699142  0.332
2012 Silversides CK, Lionel AC, Costain G, Merico D, Migita O, Liu B, Yuen T, Rickaby J, Thiruvahindrapuram B, Marshall CR, Scherer SW, Bassett AS. Rare copy number variations in adults with tetralogy of Fallot implicate novel risk gene pathways. Plos Genetics. 8: e1002843. PMID 22912587 DOI: 10.1371/Journal.Pgen.1002843  0.455
2012 Martin N, Mikhaelian M, Cytrynbaum C, Shuman C, Chitayat DA, Weksberg R, Bassett AS. 22q11.2 deletion syndrome: attitudes towards disclosing the risk of psychiatric illness. Journal of Genetic Counseling. 21: 825-34. PMID 22833231 DOI: 10.1007/S10897-012-9517-7  0.524
2012 Butcher NJ, Chow EW, Costain G, Karas D, Ho A, Bassett AS. Functional outcomes of adults with 22q11.2 deletion syndrome. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 14: 836-43. PMID 22744446 DOI: 10.1038/Gim.2012.66  0.688
2012 Husted JA, Ahmed R, Chow EW, Brzustowicz LM, Bassett AS. Early environmental exposures influence schizophrenia expression even in the presence of strong genetic predisposition. Schizophrenia Research. 137: 166-8. PMID 22381191 DOI: 10.1016/J.Schres.2012.02.009  0.465
2012 Costain G, Chow EW, Ray PN, Bassett AS. Caregiver and adult patient perspectives on the importance of a diagnosis of 22q11.2 deletion syndrome. Journal of Intellectual Disability Research : Jidr. 56: 641-51. PMID 22142442 DOI: 10.1111/J.1365-2788.2011.01510.X  0.488
2011 Costain G, Chow EW, Silversides CK, Bassett AS. Sex differences in reproductive fitness contribute to preferential maternal transmission of 22q11.2 deletions. Journal of Medical Genetics. 48: 819-24. PMID 22051516 DOI: 10.1136/Jmedgenet-2011-100440  0.525
2011 Guo T, McDonald-McGinn D, Blonska A, Shanske A, Bassett AS, Chow E, Bowser M, Sheridan M, Beemer F, Devriendt K, Swillen A, Breckpot J, Digilio MC, Marino B, Dallapiccola B, et al. Genotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients. Human Mutation. 32: 1278-89. PMID 21796729 DOI: 10.1002/Humu.21568  0.415
2011 Philip N, Bassett A. Cognitive, behavioural and psychiatric phenotype in 22q11.2 deletion syndrome Behavior Genetics. 41: 403-412. PMID 21573985 DOI: 10.1007/S10519-011-9468-Z  0.487
2011 Bassett AS, McDonald-McGinn DM, Devriendt K, Digilio MC, Goldenberg P, Habel A, Marino B, Oskarsdottir S, Philip N, Sullivan K, Swillen A, Vorstman J. Practical guidelines for managing patients with 22q11.2 deletion syndrome. The Journal of Pediatrics. 159: 332-9.e1. PMID 21570089 DOI: 10.1016/J.Jpeds.2011.02.039  0.345
2011 Bassett AS. Parental origin, DNA structure, and the schizophrenia spectrum. The American Journal of Psychiatry. 168: 350-3. PMID 21474594 DOI: 10.1176/Appi.Ajp.2011.11010173  0.462
2011 Chow EW, Ho A, Wei C, Voormolen EH, Crawley AP, Bassett AS. Association of schizophrenia in 22q11.2 deletion syndrome and gray matter volumetric deficits in the superior temporal gyrus. The American Journal of Psychiatry. 168: 522-9. PMID 21362743 DOI: 10.1176/Appi.Ajp.2010.10081230  0.566
2011 Swaby JA, Silversides CK, Bekeschus SC, Piran S, Oechslin EN, Chow EW, Bassett AS. Complex congenital heart disease in unaffected relatives of adults with 22q11.2 deletion syndrome. The American Journal of Cardiology. 107: 466-71. PMID 21257016 DOI: 10.1016/J.Amjcard.2010.09.045  0.481
2011 Piran S, Bassett AS, Grewal J, Swaby JA, Morel C, Oechslin EN, Redington AN, Liu PP, Silversides CK. Patterns of cardiac and extracardiac anomalies in adults with tetralogy of fallot. American Heart Journal. 161: 131-7. PMID 21167345 DOI: 10.1016/J.Ahj.2010.09.015  0.42
2011 Costain G, Silversides CK, Marshall CR, Shago M, Costain N, Bassett AS. 13q13.1-q13.2 deletion in tetralogy of Fallot: clinical report and a literature review. International Journal of Cardiology. 146: 134-9. PMID 20598760 DOI: 10.1016/J.Ijcard.2010.05.070  0.476
2010 Simmons TR, Flax JF, Azaro MA, Hayter JE, Justice LM, Petrill SA, Bassett AS, Tallal P, Brzustowicz LM, Bartlett CW. Increasing genotype-phenotype model determinism: application to bivariate reading/language traits and epistatic interactions in language-impaired families. Human Heredity. 70: 232-44. PMID 20948219 DOI: 10.1159/000320367  0.357
2010 Fung WLA, McEvilly R, Fong J, Silversides C, Chow E, Bassett A. Elevated prevalence of generalized anxiety disorder in adults with 22q11.2 deletion syndrome American Journal of Psychiatry. 167: 998. PMID 20693476 DOI: 10.1176/Appi.Ajp.2010.09101463  0.403
2010 Bassett AS, Costain G, Fung WL, Russell KJ, Pierce L, Kapadia R, Carter RF, Chow EW, Forsythe PJ. Clinically detectable copy number variations in a Canadian catchment population of schizophrenia. Journal of Psychiatric Research. 44: 1005-9. PMID 20643418 DOI: 10.1016/J.Jpsychires.2010.06.013  0.53
2010 Costain G, Ho A, Crawley AP, Mikulis DJ, Brzustowicz LM, Chow EW, Bassett AS. Reduced gray matter in the anterior cingulate gyrus in familial schizophrenia: a preliminary report. Schizophrenia Research. 122: 81-4. PMID 20638248 DOI: 10.1016/J.Schres.2010.06.014  0.532
2010 Husted JA, Ahmed R, Chow EW, Brzustowicz LM, Bassett AS. Childhood trauma and genetic factors in familial schizophrenia associated with the NOS1AP gene. Schizophrenia Research. 121: 187-92. PMID 20541371 DOI: 10.1016/J.Schres.2010.05.021  0.447
2010 Bassett AS, Scherer SW, Brzustowicz LM. Copy number variations in schizophrenia: critical review and new perspectives on concepts of genetics and disease. The American Journal of Psychiatry. 167: 899-914. PMID 20439386 DOI: 10.1176/Appi.Ajp.2009.09071016  0.544
2010 Voormolen EH, Wei C, Chow EW, Bassett AS, Mikulis DJ, Crawley AP. Voxel-based morphometry and automated lobar volumetry: the trade-off between spatial scale and statistical correction. Neuroimage. 49: 587-96. PMID 19619660 DOI: 10.1016/J.Neuroimage.2009.07.018  0.345
2009 Ng MY, Levinson DF, Faraone SV, Suarez BK, DeLisi LE, Arinami T, Riley B, Paunio T, Pulver AE, Irmansyah, Holmans PA, Escamilla M, Wildenauer DB, Williams NM, Laurent C, ... ... Bassett AS, et al. Meta-analysis of 32 genome-wide linkage studies of schizophrenia. Molecular Psychiatry. 14: 774-85. PMID 19349958 DOI: 10.1038/Mp.2008.135  0.503
2009 Wratten NS, Memoli H, Huang Y, Dulencin AM, Matteson PG, Cornacchia MA, Azaro MA, Messenger J, Hayter JE, Bassett AS, Buyske S, Millonig JH, Vieland VJ, Brzustowicz LM. Identification of a schizophrenia-associated functional noncoding variant in NOS1AP. The American Journal of Psychiatry. 166: 434-41. PMID 19255043 DOI: 10.1176/Appi.Ajp.2008.08081266  0.384
2009 Bassett AS, Chow EW, Husted J, Hodgkinson KA, Oechslin E, Harris L, Silversides C. Premature death in adults with 22q11.2 deletion syndrome. Journal of Medical Genetics. 46: 324-30. PMID 19246480 DOI: 10.1136/Jmg.2008.063800  0.447
2009 Zaleski C, Bassett AS, Tam K, Shugar AL, Chow EW, McPherson E. The co-occurrence of early onset Parkinson disease and 22q11.2 deletion syndrome. American Journal of Medical Genetics. Part A. 149: 525-8. PMID 19208384 DOI: 10.1002/Ajmg.A.32650  0.465
2009 Husted JA, Lim S, Chow EW, Greenwood C, Bassett AS. Heritability of neurocognitive traits in familial schizophrenia. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 845-53. PMID 19180565 DOI: 10.1002/Ajmg.B.30907  0.388
2009 Vorstman JA, Chow EW, Ophoff RA, van Engeland H, Beemer FA, Kahn RS, Sinke RJ, Bassett AS. Association of the PIK4CA schizophrenia-susceptibility gene in adults with the 22q11.2 deletion syndrome. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 430-3. PMID 18646052 DOI: 10.1002/Ajmg.B.30827  0.565
2009 Kiehl TR, Chow EW, Mikulis DJ, George SR, Bassett AS. Neuropathologic features in adults with 22q11.2 deletion syndrome. Cerebral Cortex (New York, N.Y. : 1991). 19: 153-64. PMID 18483005 DOI: 10.1093/Cercor/Bhn066  0.521
2008 Bassett AS, Marshall CR, Lionel AC, Chow EW, Scherer SW. Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome. Human Molecular Genetics. 17: 4045-53. PMID 18806272 DOI: 10.1093/Hmg/Ddn307  0.594
2008 Brzustowicz LM, Bassett AS. Phenotype matters: the case for careful characterization of relevant traits. The American Journal of Psychiatry. 165: 1096-8. PMID 18765489 DOI: 10.1176/Appi.Ajp.2008.08060897  0.493
2008 Bassett AS, Chow EW. Schizophrenia and 22q11.2 deletion syndrome. Current Psychiatry Reports. 10: 148-57. PMID 18474208 DOI: 10.1007/S11920-008-0026-1  0.577
2008 Merner ND, Hodgkinson KA, Haywood AF, Connors S, French VM, Drenckhahn JD, Kupprion C, Ramadanova K, Thierfelder L, McKenna W, Gallagher B, Morris-Larkin L, Bassett AS, Parfrey PS, Young TL. Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene. American Journal of Human Genetics. 82: 809-21. PMID 18313022 DOI: 10.1016/J.Ajhg.2008.01.010  0.361
2008 Kapadia RK, Bassett AS. Recognizing a common genetic syndrome: 22q11.2 deletion syndrome. Cmaj : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne. 178: 391-3. PMID 18268261 DOI: 10.1503/Cmaj.071300  0.405
2008 Fung WL, Chow EW, Webb GD, Gatzoulis MA, Bassett AS. Extracardiac features predicting 22q11.2 deletion syndrome in adult congenital heart disease. International Journal of Cardiology. 131: 51-8. PMID 18191243 DOI: 10.1016/J.Ijcard.2007.08.141  0.487
2007 Husted JA, Driezen P, Chow EW, Bassett AS. Sibship characteristics in a familial sample with genetic susceptibility to schizophrenia. Schizophrenia Research. 95: 248-9. PMID 17629677 DOI: 10.1093/Aje/163.Suppl_11.S218-B  0.434
2007 Bassett AS, Caluseriu O, Weksberg R, Young DA, Chow EW. Catechol-O-methyl transferase and expression of schizophrenia in 73 adults with 22q11 deletion syndrome. Biological Psychiatry. 61: 1135-40. PMID 17217925 DOI: 10.1016/J.Biopsych.2006.07.038  0.499
2007 Weksberg R, Stachon AC, Squire JA, Moldovan L, Bayani J, Meyn S, Chow E, Bassett AS. Molecular characterization of deletion breakpoints in adults with 22q11 deletion syndrome. Human Genetics. 120: 837-45. PMID 17028864 DOI: 10.1007/S00439-006-0242-X  0.51
2006 Logue MW, Brzustowicz LM, Bassett AS, Chow EW, Vieland VJ. A posterior probability of linkage-based re-analysis of schizophrenia data yields evidence of linkage to chromosomes 1 and 17. Human Heredity. 62: 47-54. PMID 17019084 DOI: 10.1159/000096035  0.494
2006 Chow EW, Watson M, Young DA, Bassett AS. Neurocognitive profile in 22q11 deletion syndrome and schizophrenia. Schizophrenia Research. 87: 270-8. PMID 16753283 DOI: 10.1016/J.Schres.2006.04.007  0.501
2006 Caluseriu O, Mirza G, Ragoussis J, Chow EW, MacCrimmon D, Bassett AS. Schizophrenia in an adult with 6p25 deletion syndrome. American Journal of Medical Genetics. Part A. 140: 1208-13. PMID 16642507 DOI: 10.1002/Ajmg.A.31222  0.488
2006 Talkowski ME, Seltman H, Bassett AS, Brzustowicz LM, Chen X, Chowdari KV, Collier DA, Cordeiro Q, Corvin AP, Deshpande SN, Egan MF, Gill M, Kendler KS, Kirov G, Heston LL, et al. Evaluation of a susceptibility gene for schizophrenia: genotype based meta-analysis of RGS4 polymorphisms from thirteen independent samples. Biological Psychiatry. 60: 152-62. PMID 16631129 DOI: 10.1016/J.Biopsych.2006.02.015  0.348
2006 Husted JA, Greenwood CM, Bassett AS. Heritability of schizophrenia and major affective disorder as a function of age, in the presence of strong cohort effects. European Archives of Psychiatry and Clinical Neuroscience. 256: 222-9. PMID 16331352 DOI: 10.1007/S00406-005-0629-Z  0.418
2005 Weksberg R, Hughes S, Moldovan L, Bassett AS, Chow EW, Squire JA. A method for accurate detection of genomic microdeletions using real-time quantitative PCR. Bmc Genomics. 6: 180. PMID 16351727 DOI: 10.1186/1471-2164-6-180  0.411
2005 Bassett AS, Chow EW, Husted J, Weksberg R, Caluseriu O, Webb GD, Gatzoulis MA. Clinical features of 78 adults with 22q11 Deletion Syndrome. American Journal of Medical Genetics. Part A. 138: 307-13. PMID 16208694 DOI: 10.1002/Ajmg.A.30984  0.456
2005 Moore SJ, Green JS, Fan Y, Bhogal AK, Dicks E, Fernandez BA, Stefanelli M, Murphy C, Cramer BC, Dean JC, Beales PL, Katsanis N, Bassett AS, Davidson WS, Parfrey PS. Clinical and genetic epidemiology of Bardet-Biedl syndrome in Newfoundland: a 22-year prospective, population-based, cohort study. American Journal of Medical Genetics. Part A. 132: 352-60. PMID 15637713 DOI: 10.1002/Ajmg.A.30406  0.369
2005 Saviouk V, Chow EW, Bassett AS, Brzustowicz LM. Tumor necrosis factor promoter haplotype associated with schizophrenia reveals a linked locus on 1q44. Molecular Psychiatry. 10: 375-83. PMID 15340354 DOI: 10.1038/Sj.Mp.4001582  0.518
2004 Greenwood CM, Husted J, Bomba MD, Hodgkinson KA, Bassett AS. Elevated rates of schizophrenia in a familial sample with mental illness and intellectual disability. Journal of Intellectual Disability Research : Jidr. 48: 531-9. PMID 15312053 DOI: 10.1111/J.1365-2788.2004.00621.X  0.459
2004 Martín B, Fañanás L, Gutiérrez B, Chow EW, Bassett AS. Dermatoglyphic profile in 22q deletion syndrome. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 128: 46-9. PMID 15211630 DOI: 10.1002/Ajmg.B.30034  0.513
2004 Brzustowicz LM, Simone J, Mohseni P, Hayter JE, Hodgkinson KA, Chow EW, Bassett AS. Linkage disequilibrium mapping of schizophrenia susceptibility to the CAPON region of chromosome 1q22. American Journal of Human Genetics. 74: 1057-63. PMID 15065015 DOI: 10.1086/420774  0.532
2003 Chow EW, Husted J, Weksberg R, Bassett AS. Postmaturity in a genetic subtype of schizophrenia. Acta Psychiatrica Scandinavica. 108: 260-8. PMID 12956826 DOI: 10.1034/J.1600-0447.2003.00124.X  0.47
2003 Bassett AS, Chow EW, AbdelMalik P, Gheorghiu M, Husted J, Weksberg R. The schizophrenia phenotype in 22q11 deletion syndrome. The American Journal of Psychiatry. 160: 1580-6. PMID 12944331 DOI: 10.1176/Appi.Ajp.160.9.1580  0.506
2003 Lewis CM, Levinson DF, Wise LH, DeLisi LE, Straub RE, Hovatta I, Williams NM, Schwab SG, Pulver AE, Faraone SV, Brzustowicz LM, Kaufmann CA, Garver DL, Gurling HM, Lindholm E, ... ... Bassett AS, et al. Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia. American Journal of Human Genetics. 73: 34-48. PMID 12802786 DOI: 10.1086/376549  0.537
2003 AbdelMalik P, Husted J, Chow EW, Bassett AS. Childhood head injury and expression of schizophrenia in multiply affected families. Archives of General Psychiatry. 60: 231-6. PMID 12622655 DOI: 10.1001/Archpsyc.60.3.231  0.387
2003 Gheorghiu M, Chow E, Bassett A. Childhood behaviour in a 22Q deletion syndrome subtype of schizophrenia Schizophrenia Research. 60: 81. DOI: 10.1016/S0920-9964(03)80627-8  0.49
2003 Chow E, Weksberg R, Bassett A. Impulsivity and aggression in 22Q11 deletion syndrome and schizophrenia Schizophrenia Research. 60: 79. DOI: 10.1016/S0920-9964(03)80621-7  0.488
2003 Caluseriu O, Tayyeb T, Chow E, Bassett A. Clozapine-associated seizures in a 22Q deletion syndrome subtype of schizophrenia Schizophrenia Research. 60: 79. DOI: 10.1016/S0920-9964(03)80620-5  0.434
2003 Bassett AS, Chow E, AbdelMalik P, Gheorghiu M, Husted J, Weksberg R. The schizophrenia phenotype in 22Q deletion syndrome Schizophrenia Research. 60: 78. DOI: 10.1016/S0920-9964(03)80618-7  0.578
2003 AbdelMalik P, Bassett A, Husted J, Chow E. Childhood head injury and illness expression in familial schizophrenia Schizophrenia Research. 60: 77. DOI: 10.1016/S0920-9964(03)80613-8  0.372
2002 Brzustowicz LM, Hayter JE, Hodgkinson KA, Chow EW, Bassett AS. Fine mapping of the schizophrenia susceptibility locus on chromosome 1q22. Human Heredity. 54: 199-209. PMID 12771552 DOI: 10.1159/000070665  0.506
2002 Bassett AS, Chow EW, Vieland VJ, Brzustowicz L. Is schizophrenia linked to chromosome 1q? Science (New York, N.Y.). 298: 2277; author reply 2. PMID 12494945 DOI: 10.1126/Science.1076508  0.532
2002 Bassett AS, Chow EW, Weksberg R, Brzustowicz L. Schizophrenia and genetics: new insights. Current Psychiatry Reports. 4: 307-14. PMID 12126600 DOI: 10.1007/S11920-996-0051-X  0.519
2002 Bartlett CW, Flax JF, Logue MW, Vieland VJ, Bassett AS, Tallal P, Brzustowicz LM. A major susceptibility locus for specific language impairment is located on 13q21. American Journal of Human Genetics. 71: 45-55. PMID 12048648 DOI: 10.1086/341095  0.345
2002 Waterwort DM, Bassett AS, Brzustowicz LM. Recent advances in the genetics of schizophrenia. Cellular and Molecular Life Sciences : Cmls. 59: 331-48. PMID 11915947 DOI: 10.1007/S00018-002-8426-6  0.569
2002 Chow EW, Zipursky RB, Mikulis DJ, Bassett AS. Structural brain abnormalities in patients with schizophrenia and 22q11 deletion syndrome. Biological Psychiatry. 51: 208-15. PMID 11839363 DOI: 10.1016/S0006-3223(01)01246-X  0.568
2002 Zwaigenbaum L, Chow E, Bassett A, Farrell S. Behavioural Disorders in Children with Cleft Palate and 22Q11 Deletion Syndrome Paediatrics & Child Health. 7: 56A-56A. DOI: 10.1093/pch/7.suppl_A.56Aa  0.307
2001 Scutt LE, Chow EW, Weksberg R, Honer WG, Bassett AS. Patterns of dysmorphic features in schizophrenia. American Journal of Medical Genetics. 105: 713-23. PMID 11803519 DOI: 10.1002/Ajmg.1612  0.426
2001 Bassett AS, Chow EW, O'Neill S, Brzustowicz LM. Genetic insights into the neurodevelopmental hypothesis of schizophrenia. Schizophrenia Bulletin. 27: 417-30. PMID 11596844 DOI: 10.1093/Oxfordjournals.Schbul.A006884  0.477
2001 Kopala LC, Good KP, Morrison K, Bassett AS, Alda M, Honer WG. Impaired olfactory identification in relatives of patients with familial schizophrenia. The American Journal of Psychiatry. 158: 1286-90. PMID 11481164 DOI: 10.1176/Appi.Ajp.158.8.1286  0.396
2001 Lazier K, Chow EW, AbdelMalik P, Scutt LE, Weksberg R, Bassett AS. Low platelet count in a 22q11 deletion syndrome subtype of schizophrenia. Schizophrenia Research. 50: 177-80. PMID 11439238 DOI: 10.1016/S0920-9964(00)00159-6  0.477
2001 Bassett AS, Chow EW, Waterworth DM, Brzustowicz L. Genetic insights into schizophrenia. Canadian Journal of Psychiatry. Revue Canadienne De Psychiatrie. 46: 131-7. PMID 11280081 DOI: 10.1177/070674370104600203  0.492
2001 Hodgkinson KA, Murphy J, O'Neill S, Brzustowicz L, Bassett AS. Genetic counselling for schizophrenia in the era of molecular genetics. Canadian Journal of Psychiatry. Revue Canadienne De Psychiatrie. 46: 123-30. PMID 11280080 DOI: 10.1177/070674370104600202  0.456
2001 Bassett AS. Psychiatric genetics in the 21st century. Canadian Journal of Psychiatry. Revue Canadienne De Psychiatrie. 46: 121-2. PMID 11280079 DOI: 10.1177/070674370104600201  0.311
2001 Bassett AS, Chow EWC, Brzustowicz L. The genetics of schizophrenia Neuroscience News. 4: 20-26.  0.353
2000 Bassett AS, Chow EW, Weksberg R. Chromosomal abnormalities and schizophrenia. American Journal of Medical Genetics. 97: 45-51. PMID 10813803 DOI: 10.1002/(Sici)1096-8628(200021)97:1<45::Aid-Ajmg6>3.0.Co;2-9  0.563
2000 Brzustowicz LM, Hodgkinson KA, Chow EW, Honer WG, Bassett AS. Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22. Science (New York, N.Y.). 288: 678-82. PMID 10784452 DOI: 10.1126/Science.288.5466.678  0.572
2000 Nicolson R, Murphy K, Chow E, Zipursky R, Bassett A. 379. 22q11 deletion syndrome (velocardiofacial syndrome) and schizophrenia: a genetic subtype? Biological Psychiatry. 47: S115-S116. DOI: 10.1016/S0006-3223(00)00643-0  0.559
1999 Chow EW, Mikulis DJ, Zipursky RB, Scutt LE, Weksberg R, Bassett AS. Qualitative MRI findings in adults with 22q11 deletion syndrome and schizophrenia. Biological Psychiatry. 46: 1436-42. PMID 10578458 DOI: 10.1016/S0006-3223(99)00150-X  0.533
1999 Bassett AS, Chow EW. 22q11 deletion syndrome: a genetic subtype of schizophrenia. Biological Psychiatry. 46: 882-91. PMID 10509171 DOI: 10.1016/S0006-3223(99)00114-6  0.563
1999 Cohen E, Chow EW, Weksberg R, Bassett AS. Phenotype of adults with the 22q11 deletion syndrome: A review. American Journal of Medical Genetics. 86: 359-65. PMID 10494092 DOI: 10.1002/(Sici)1096-8628(19991008)86:4<359::Aid-Ajmg10>3.0.Co;2-V  0.405
1999 Brzustowicz LM, Honer WG, Chow EW, Little D, Hogan J, Hodgkinson K, Bassett AS. Linkage of familial schizophrenia to chromosome 13q32. American Journal of Human Genetics. 65: 1096-103. PMID 10486329 DOI: 10.1086/302579  0.532
1999 Chow E, Young D, Janiszewski E, Tso A, Weksberg R, Bassett AS. Neurocognitive functioning in adult patients with 22q11 deletion syndrome and schizophrenia Genetic Counseling. 10: 112.  0.463
1999 Bassett AS, Chow E, Scltt L, Hüücmmün K, Weksberg R. Adult phenotype of 22q11 deletion syndrome and schizophrenia Genetic Counseling. 10: 111-112.  0.486
1998 Bassett AS. Progress on the genetics of schizophrenia. Journal of Psychiatry & Neuroscience : Jpn. 23: 270-3. PMID 9846030  0.357
1998 Neves-Pereira M, Bassett AS, Honer WG, Lang D, King NA, Kennedy JL. No evidence for linkage of the CHRNA7 gene region in Canadian schizophrenia families. American Journal of Medical Genetics. 81: 361-3. PMID 9754620 DOI: 10.1002/(Sici)1096-8628(19980907)81:5<361::Aid-Ajmg3>3.0.Co;2-W  0.407
1998 Bassett AS, Hodgkinson K, Chow EW, Correia S, Scutt LE, Weksberg R. 22q11 deletion syndrome in adults with schizophrenia. American Journal of Medical Genetics. 81: 328-37. PMID 9674980 DOI: 10.1002/(Sici)1096-8628(19980710)81:4<328::Aid-Ajmg10>3.0.Co;2-N  0.592
1998 Husted J, Scutt LE, Bassett AS. Paternal transmission and anticipation in schizophrenia. American Journal of Medical Genetics. 81: 156-62. PMID 9613855 DOI: 10.1002/(Sici)1096-8628(19980328)81:2<156::Aid-Ajmg6>3.0.Co;2-U  0.384
1998 Petronis A, Vincent J, Paterson A, Bassett A, Honer W, Gottesman I, Fuller Torrey E, Meltzer H, Lieberman J, Kennedy J. Search for unstable DNA in schizophrenia Schizophrenia Research. 29: 135. DOI: 10.1016/S0920-9964(97)88642-2  0.384
1998 Scutt L, Correia S, Chow E, Hogan J, Hodgkinson K, Jones C, Honer W, Kaegi S, Weksberg R, Bassett A. Delineating a 22q11 deletion subtype of schizophrenia Schizophrenia Research. 29: 131. DOI: 10.1016/S0920-9964(97)88631-8  0.468
1998 Bassett A, Hodgkinson K, Chow E, Scutt L, Weksberg R. 22q11.2 deletion syndrome and schizophrenia Schizophrenia Research. 29: 131. DOI: 10.1016/S0920-9964(97)88630-6  0.489
1997 Erlenmeyer-Kimling L, Adamo UH, Rock D, Roberts SA, Bassett AS, Squires-Wheeler E, Cornblatt BA, Endicott J, Pape S, Gottesman II. The New York High-Risk Project. Prevalence and comorbidity of axis I disorders in offspring of schizophrenic parents at 25-year follow-up. Archives of General Psychiatry. 54: 1096-102. PMID 9400345 DOI: 10.1001/Archpsyc.1997.01830240052008  0.355
1997 Brzustowicz LM, Honer WG, Chow EW, Hogan J, Hodgkinson K, Bassett AS. Use of a quantitative trait to map a locus associated with severity of positive symptoms in familial schizophrenia to chromosome 6p. American Journal of Human Genetics. 61: 1388-96. PMID 9399881 DOI: 10.1086/301623  0.479
1997 Smith GN, Flynn SW, Kopala LC, Bassett AS, Lapointe JS, Falkai P, Honer WG. A comprehensive method of assessing routine CT scans in schizophrenia. Acta Psychiatrica Scandinavica. 96: 395-401. PMID 9395159 DOI: 10.1111/J.1600-0447.1997.Tb09935.X  0.373
1997 King N, Bassett AS, Honer WG, Masellis M, Kennedy JL. Absence of linkage for schizophrenia on the short arm of chromosome 5 in multiplex Canadian families. American Journal of Medical Genetics. 74: 472-4. PMID 9342193 DOI: 10.1002/(Sici)1096-8628(19970919)74:5<472::Aid-Ajmg2>3.0.Co;2-Q  0.47
1997 Vicente AM, Macciardi F, Verga M, Bassett AS, Honer WG, Bean G, Kennedy JL. NCAM and schizophrenia: genetic studies. Molecular Psychiatry. 2: 65-9. PMID 9154219 DOI: 10.1038/Sj.Mp.4000235  0.477
1997 Lang DJ, Bassett AS, Falkai P, Smith GN, Lapointe JS, Honer WG. Sylvian fissure and middle cranial fossae asymmetries in families with schizophrenia Schizophrenia Research. 24: 150. DOI: 10.1016/S0920-9964(97)82429-2  0.427
1997 Bassett A, Scutt L, Correia S, Bomba M, Husted J. Anticipation and imprinting in schizophrenia: Results from a large representative Canadian archival sample Schizophrenia Research. 24: 54. DOI: 10.1016/S0920-9964(97)82155-X  0.421
1997 Bury A, Chow E, Weksberg R, Correia S, Scutt L, Bassett A. Velocardiofacial syndrome (VCFS) in schizophrenia: Cognitive features Schizophrenia Research. 24: 53. DOI: 10.1016/S0920-9964(97)82152-4  0.43
1997 Hodgkinson K, Chow E, Correia S, Scutt L, McAlduff J, Beatty B, Squire J, Weksberg R, Bassett A. Velo-Cardio-Facial Syndrome: A true genetic subtype of schizophrenia? Schizophrenia Research. 24: 53. DOI: 10.1016/S0920-9964(97)82151-2  0.393
1997 Bassett A, Honer W, Chow E, McAlduff J, Hodgkinson K, Kirkham S, Brzustowicz L. A susceptibility locus for schizophrenia on chromosome 6 using positive symptom scores as quantitative traits Schizophrenia Research. 24: 50. DOI: 10.1016/S0920-9964(97)82143-3  0.362
1996 O'Malley MP, Bassett AS, Honer WG, Kennedy JL, King N, Berg D. Linkage analysis between schizophrenia and the Darier's disease region on 12q. Psychiatric Genetics. 6: 187-90. PMID 9149323 DOI: 10.1097/00041444-199624000-00003  0.521
1996 Bassett AS, Chow EW, Bury A, Ali F, Haylock CA, Smith GN, Lapointe JS, Honer WG. Increased head circumference in schizophrenia. Biological Psychiatry. 40: 1173-5. PMID 8931921 DOI: 10.1016/S0006-3223(96)00288-0  0.37
1996 Bassett AS, Bury A, Hodgkinson KA, Honer WG. Reproductive fitness in familial schizophrenia. Schizophrenia Research. 21: 151-60. PMID 8885043 DOI: 10.1016/0920-9964(96)00018-7  0.466
1996 Honer WG, Bassett AS, Falkai P, Beach TG, Lapointe JS. A case study of temporal lobe development in familial schizophrenia. Psychological Medicine. 26: 191-5. PMID 8643758  0.354
1996 Wakem P, Ikeda S, Haake A, Polakowska R, Ewing N, Sarret Y, Duvic M, Berg D, Bassett A, Kennedy JL, Tuskis A, Epstein EH, Goldsmith LA. Localization of the Darier Disease Gene to a 2-cM Portion of 12q23-24.1 Journal of Investigative Dermatology. 106: 365-367. PMID 8601743 DOI: 10.1111/1523-1747.Ep12343145  0.344
1996 Brzustowicz LM, Honer WG, McAlduff J, Hodgkinson K, Ricketts AR, Bassett AS. Evidence for a locus on chromosome 6p related to positive symptom scores in Canadian families with schizophrenia Psychiatric Genetics. 6: 137. DOI: 10.1097/00041444-199623000-00010  0.453
1996 Kopala L, Bassett A, Morrison K, Good K, Honer W. Olfactory deficits in familial schizophrenia Schizophrenia Research. 18: 244. DOI: 10.1016/0920-9964(96)85741-0  0.409
1996 Honer W, Bassett A, Squires-Wheeler E, Falkai P, Smith G, Lapointe J, Canero C, Lang D. The temporal lobes, reversed asymmetry, and schizophrenia genetics Schizophrenia Research. 18: 184. DOI: 10.1016/0920-9964(96)85578-2  0.33
1995 Honer WG, Bassett AS, Squires-Wheeler E, Falkai P, Smith GN, Lapointe JS, Canero C, Lang DJ. The temporal lobes, reversed asymmetry and the genetics of schizophrenia. Neuroreport. 7: 221-4. PMID 8742456 DOI: 10.1097/00001756-199512290-00053  0.447
1995 Erlenmeyer-Kimling L, Squires-Wheeler E, Adamo UH, Bassett AS, Cornblatt BA, Kestenbaum CJ, Rock D, Roberts SA, Gottesman II. The New York High-Risk Project. Psychoses and cluster A personality disorders in offspring of schizophrenic parents at 23 years of follow-up. Archives of General Psychiatry. 52: 857-65. PMID 7575106 DOI: 10.1001/Archpsyc.1995.03950220067013  0.375
1995 Kennedy JL, Berg D, Bassett AS, Roy R, King N, Perkins M. Genetic linkage for Darier disease (keratosis follicularis). American Journal of Medical Genetics. 55: 307-10. PMID 7537018 DOI: 10.1002/Ajmg.1320550312  0.403
1995 Petronis A, Sasaki T, Bassett A, Honer W, Kennedy J. Search for unstable DNA in schizophrenia families demonstrating evidence for genetic anticipation Schizophrenia Research. 15: 46. DOI: 10.1016/0920-9964(95)95149-4  0.415
1995 Vicente A, Sasaki T, King N, Barr C, Bassett A, Honer W, Macciardi F, Kennedy J. Genetic testing of the neurodevelopment hypothesis of schizophrenia Schizophrenia Research. 15: 42. DOI: 10.1016/0920-9964(95)95136-W  0.441
1995 Honer WG, Bassett AS, Canero C, Smith GN, Lapointe JS, Squires-Wheeler E, Falkai P. The temporal lobe in families with schizophrenia: Effects of diagnosis and family of origin Schizophrenia Research. 15: 41. DOI: 10.1016/0920-9964(95)95131-R  0.377
1995 Hodgkinson KA, Macgregor DJ, Shuman C, Bassett AS. The provision of genetic counselling for persons with schizophrenia and their relatives Schizophrenia Research. 15: 40. DOI: 10.1016/0920-9964(95)95130-2  0.45
1994 Bassett AS, Honer WG. Evidence for anticipation in schizophrenia. American Journal of Human Genetics. 54: 864-70. PMID 8178826  0.378
1994 Chow EW, Bassett AS, Weksberg R. Velo-cardio-facial syndrome and psychotic disorders: implications for psychiatric genetics. American Journal of Medical Genetics. 54: 107-12. PMID 8074160 DOI: 10.1002/Ajmg.1320540205  0.525
1994 Bassett AS, Bury A, Honer WG. Testing Liddle's three-syndrome model in families with schizophrenia. Schizophrenia Research. 12: 213-21. PMID 8054313 DOI: 10.1016/0920-9964(94)90031-0  0.423
1994 Sidenberg DG, Berg D, Bassett AS, King N, Petronis A, Kamble AB, Kennedy JL. Genetic linkage evaluation of twenty-four loci in an eastern Canadian family segregating Darier's disease (keratosis follicularis). Journal of the American Academy of Dermatology. 31: 27-30. PMID 8021367 DOI: 10.1016/S0190-9622(94)70130-X  0.384
1994 Honer WG, Bassett AS, Smith GN, Lapointe JS, Falkai P. Temporal lobe abnormalities in multigenerational families with schizophrenia. Biological Psychiatry. 36: 737-43. PMID 7858069 DOI: 10.1016/0006-3223(94)90084-1  0.412
1993 Bassett AS, Collins EJ, Nuttall SE, Honer WG. Positive and negative symptoms in families with schizophrenia. Schizophrenia Research. 11: 9-19. PMID 8297809 DOI: 10.1016/0920-9964(93)90033-F  0.446
1993 Sidenberg DG, Bassett AS, Demchyshyn L, Niznik HB, Macciardi F, Kamble AB, Honer WG, Kennedy JL. New polymorphism for the human serotonin 1D receptor variant (5-HT1D beta) not linked to schizophrenia in five Canadian pedigrees. Human Heredity. 43: 315-8. PMID 8104876 DOI: 10.1159/000154150  0.394
1993 Petronis A, Bassett A, Sidenberg D, Kamble A, Honer W, Macciardi F, Kennedy J. Investigation of genetic risk factors for schizophrenia on 11q Schizophrenia Research. 9: 122. DOI: 10.1016/0920-9964(93)90183-J  0.534
1993 Kennedy J, Van Tol H, Petronis A, Sidenberg D, Macciardi F, Honer W, Bassett A. Dopamine D4 receptor gene variants and schizophrenia Schizophrenia Research. 9: 119. DOI: 10.1016/0920-9964(93)90173-G  0.377
1993 Jones C, Bassett A, McGillivray B, Weksberg R, Roy R, MacEwan G, Smith G, Lang M, Homer W. Physical anomalies in schizophrenia Schizophrenia Research. 9: 118. DOI: 10.1016/0920-9964(93)90170-N  0.309
1992 Honer WG, Bassett AS, MacEwan GW, Hurwitz T, Li DK, Hilal S, Prohovnik I. Structural brain imaging abnormalities associated with schizophrenia and partial trisomy of chromosome 5. Psychological Medicine. 22: 519-24. PMID 1615118 DOI: 10.1017/S0033291700030464  0.464
1992 Bassett AS. Chromosomal aberrations and schizophrenia. Autosomes. The British Journal of Psychiatry : the Journal of Mental Science. 161: 323-34. PMID 1393302 DOI: 10.1192/Bjp.161.3.323  0.543
1991 Kopala LC, Clark CC, Bassett A. Olfactory deficits in schizophrenia and chromosome 5. Biological Psychiatry. 29: 732-733. PMID 2054445 DOI: 10.1016/0006-3223(91)90151-B  0.466
1991 Bassett AS. Linkage analysis of schizophrenia: challenges and promise. Social Biology. 38: 189-96. PMID 1801200 DOI: 10.1080/19485565.1991.9988787  0.501
1991 Honer W, Bassett A, MacEwan G, Hurwitz T, Li D, Hilal S, Prohovnik I. Structural brain imaging in partial trisomy chromosome 5 with schizophrenia Schizophrenia Research. 4: 278. DOI: 10.1016/0920-9964(91)90144-G  0.325
1991 Bassett A, Collins E, Honer W, McAlduff J, Forsythe P. Genetic linkage analysis study of schizophrenia in Canadian families: Clinical assessment results Schizophrenia Research. 4: 249. DOI: 10.1016/0920-9964(91)90093-7  0.451
1991 Bassett A. Chromosomal aberrations and schizophrenia Schizophrenia Research. 4: 248-249. DOI: 10.1016/0920-9964(91)90092-6  0.493
1990 Honer WG, Bassett AS, Kopala L, Kennedy JL. A genotype-phenotype research strategy for schizophrenia. Canadian Journal of Psychiatry. Revue Canadienne De Psychiatrie. 35: 776-83. PMID 2282633 DOI: 10.1177/070674379003500910  0.436
1990 McGillivray BC, Bassett AS, Langlois S, Pantzar T, Wood S. Familial 5q11.2----q13.3 segmental duplication cosegregating with multiple anomalies, including schizophrenia. American Journal of Medical Genetics. 35: 10-3. PMID 1967903 DOI: 10.1002/ajmg.1320350103  0.458
1989 Bassett AS. Chromosome 5 and schizophrenia: implications for genetic linkage studies. Schizophrenia Bulletin. 15: 393-402. PMID 2814372 DOI: 10.1093/schbul/15.3.393  0.401
1989 Gilliam TC, Freimer NB, Kaufmann CA, Powchik PP, Bassett AS, Bengtsson U, Wasmuth JJ. Deletion mapping of DNA markers to a region of chromosome 5 that cosegregates with schizophrenia. Genomics. 5: 940-4. PMID 2591972 DOI: 10.1016/0888-7543(89)90138-9  0.4
1989 Bassett AS. Eye Tracking Dysfunction is Associated With Partial Trisomy of Chromosome 5 and Schizophrenia: A Response-Reply Archives of General Psychiatry. 46: 757. DOI: 10.1001/archpsyc.1989.01810080087014  0.374
1988 Iacono WG, Bassett AS, Jones BD. Eye tracking dysfunction is associated with partial trisomy of chromosome 5 and schizophrenia. Archives of General Psychiatry. 45: 1140-1. PMID 3196143 DOI: 10.1001/archpsyc.1988.01800360088014  0.393
1988 Bassett AS, McGillivray BC, Jones BD, Pantzar JT. Partial trisomy chromosome 5 cosegregating with schizophrenia. Lancet. 1: 799-801. PMID 2895320  0.414
Low-probability matches (unlikely to be authored by this person)
1997 Bassett AS, Husted J. Anticipation or ascertainment bias in schizophrenia? Penrose's familial mental illness sample. American Journal of Human Genetics. 60: 630-7. PMID 9042924  0.299
2015 Lowther C, Costain G, Bassett AS. Reproductive genetic testing and human genetic variation in the era of genomic medicine. The American Journal of Bioethics : Ajob. 15: 25-6. PMID 26030491 DOI: 10.1080/15265161.2015.1028661  0.299
2010 Husted JA, Greenwood C, Bassett AS. Re: Familial aggregation of clinical and neurocognitive features in sibling pairs with and without schizophrenia. Schizophrenia Research. 116: 289-90. PMID 19926455 DOI: 10.1016/j.schres.2009.08.019  0.297
2023 Cancelliere S, Heung T, Fischbach S, Klaiman P, Bassett AS. Adult-onset obstructive sleep apnea and pediatric pharyngoplasty in 22q11.2 deletion syndrome. Sleep Medicine. 104: 49-55. PMID 36889031 DOI: 10.1016/j.sleep.2023.02.010  0.291
1993 Bury A, Nuttall S, Roy R, McAlduff J, Dufour K, Honer W, Bassett A. Replication of Liddle's three syndromes in a familial sample Schizophrenia Research. 9: 95. DOI: 10.1016/0920-9964(93)90097-3  0.289
2021 Blagojevic C, Heung T, Theriault M, Tomita-Mitchell A, Chakraborty P, Kernohan K, Bulman DE, Bassett AS. Estimate of the contemporary live-birth prevalence of recurrent 22q11.2 deletions: a cross-sectional analysis from population-based newborn screening. Cmaj Open. 9: E802-E809. PMID 34404688 DOI: 10.9778/cmajo.20200294  0.289
2019 Stahel P, Nahmias A, Sud SK, Lee SJ, Pucci A, Yousseif A, Yosseff A, Jackson T, Urbach DR, Okrainec A, Allard JP, Sockalingam S, Yao J, Barua M, Jiao H, ... ... Bassett AS, et al. Evaluation of the Genetic Association Between Adult Obesity and Neuropsychiatric Disease. Diabetes. PMID 31506345 DOI: 10.2337/Db18-1254  0.287
2021 Palmer LD, Heung T, Corral M, Boot E, Brooks SG, Bassett AS. Sexual knowledge and behaviour in 22q11.2 deletion syndrome, a complex care condition. Journal of Applied Research in Intellectual Disabilities : Jarid. PMID 34291536 DOI: 10.1111/jar.12927  0.286
2015 Bassett A, Costain G, Marshall C, Scherer S, Ogura L, Merico D, Silversides C. MICRORNAS AND GENETIC RISK FOR TETRALOGY OF FALLOT Canadian Journal of Cardiology. 31: S189-S190. DOI: 10.1016/J.Cjca.2015.07.401  0.285
2018 Stahel P, Sud S, Lee SJ, Bassett A, Paterson A, Sockalingam S, Dash S. Phenotypic and Genetic Analysis of Adults with Extreme Obesity Canadian Journal of Diabetes. 42: S37. DOI: 10.1016/J.Jcjd.2018.08.109  0.283
2022 Blagojevic C, Heung T, Malecki S, Ying S, Cancelliere S, Hegele R, Bassett A. Hypertriglyceridemia in young adults with a 22q11.2 microdeletion. European Journal of Endocrinology. PMID 35521712 DOI: 10.1530/EJE-21-1104  0.281
2017 Lowther C, Costain G, Baribeau DA, Bassett AS. Genomic Disorders in Psychiatry-What Does the Clinician Need to Know? Current Psychiatry Reports. 19: 82. PMID 28929285 DOI: 10.1007/S11920-017-0831-5  0.28
2018 Stahel P, Sud SK, Lee SJ, Jackson T, Urbach DR, Okrainec A, Allard JP, Bassett AS, Paterson AD, Sockalingam S, Dash S. Phenotypic and genetic analysis of an adult cohort with extreme obesity. International Journal of Obesity (2005). PMID 30242240 DOI: 10.1038/S41366-018-0209-8  0.275
2003 Good KP, Kopala LC, Bassett A, Morrison K, Honer WG. Microsmia in postmenopausal women with genetic vulnerability to psychosis [3] Schizophrenia Research. 61: 327-328. PMID 12729886 DOI: 10.1016/S0920-9964(02)00229-3  0.274
1998 Roberts S, Scutt L, Bassett A, Honer W, Chow E. Cognitive impairment and genetic risk in familial schizophrenia: Assessment of performance on the mini-mental state examination (MMSE) Schizophrenia Research. 29: 137-138. DOI: 10.1016/S0920-9964(97)88649-5  0.273
1995 Erlenmeyer-Kimling L, Squires-Wheeler E, Hilldof-Adamo U, Bassett AS, Cornblatt BA, Rock D, Roberts S, Gottesman II. The New York high-risk project: Major axis I disorders in the adult offspring of schizophrenic parents Schizophrenia Research. 15: 38. DOI: 10.1016/0920-9964(95)95123-Q  0.273
2021 Fiksinski AM, Bearden CE, Bassett AS, Kahn RS, Zinkstok JR, Hooper SR, Tempelaar W, Vorstman JAS, Breetvelt EJ. A normative chart for cognitive development in a genetically selected population. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. PMID 33782512 DOI: 10.1038/s41386-021-00988-6  0.272
2011 Bassett AS. Commentary: Anxiety Disorders and Perceptual Disturbances in Adolescents with 22q11.2 Deletion Syndrome Treated with SSRI: A Case Series. Journal of the Canadian Academy of Child and Adolescent Psychiatry = Journal De L'AcadéMie Canadienne De Psychiatrie De L'Enfant Et De L'Adolescent. 20: 311. PMID 22114613  0.261
1991 Squires-Wheeler E, Erlenmeyer-Kimling L, Adamo U, Bassett A, Cornblatt B, Roberts S. Axis II personality features and disorder in subjects in the New York high-risk project Schizophrenia Research. 4: 284-285. DOI: 10.1016/0920-9964(91)90156-L  0.254
1991 Bassett AS, Beiser M. DSM-III: use of the multiaxial diagnostic system in clinical practice. Canadian Journal of Psychiatry. Revue Canadienne De Psychiatrie. 36: 270-4. PMID 1868420 DOI: 10.1177/070674379103600406  0.251
1995 Erlenmeyer-Kimling L, Squires-Wheeler E, Hilldofl-Adamo U, Bassett AS, Cornblatt BA, Rock D, Roberts S, Gottesman II. The new york high-risk project: Psychoses in the adult offspring of schizophrenic parents Schizophrenia Research. 15: 38. DOI: 10.1016/0920-9964(95)95122-P  0.248
2018 Reuter MS, Jobling R, Chaturvedi RR, Manshaei R, Costain G, Heung T, Curtis M, Hosseini SM, Liston E, Lowther C, Oechslin E, Sticht H, Thiruvahindrapuram B, Mil SV, Wald RM, ... ... Bassett AS, et al. Haploinsufficiency of vascular endothelial growth factor related signaling genes is associated with tetralogy of Fallot. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 30232381 DOI: 10.1038/S41436-018-0260-9  0.245
2022 Boot E, Marras C, Bassett AS. Spectrum of movement disorders and motor abnormalities in adults with a 22q11.2 microdeletion: Comment on the literature and retrospective study of 92 adults. European Journal of Human Genetics : Ejhg. PMID 36002662 DOI: 10.1038/s41431-022-01152-4  0.244
2010 Lanctôt KL, Rapoport MJ, Chan F, Rajaram RD, Strauss J, Sicard T, McCullagh S, Feinstein A, Kiss A, Kennedy JL, Bassett AS, Herrmann N. Genetic predictors of response to treatment with citalopram in depression secondary to traumatic brain injury. Brain Injury. 24: 959-69. PMID 20515362 DOI: 10.3109/02699051003789229  0.244
2021 Skoric-Milosavljevic D, Tadros R, Bosada FM, Tessadori F, van Weerd JH, Woudstra OI, Tjong FVY, Lahrouchi N, Bajolle F, Cordell HJ, Agopian AJ, Blue GM, Barge-Schaapveld DQ, Gewillig MH, Preuss C, ... ... Bassett AS, et al. Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries. Circulation Research. PMID 34886679 DOI: 10.1161/CIRCRESAHA.120.317107  0.243
2017 Andrade DM, Bassett AS, Bercovici E, Borlot F, Bui E, Camfield P, Clozza GQ, Cohen E, Gofine T, Graves L, Greenaway J, Gutman B, Guttman-Slater M, Hassan A, Henze M, et al. Epilepsy: Transition from pediatric to adult care. Recommendations of the Ontario epilepsy implementation task force. Epilepsia. PMID 28681381 DOI: 10.1111/Epi.13832  0.241
1996 Petronis A, Bassett AS, Honer WG, Vincent JB, Tatuch Y, Sasaki T, Ying DJ, Klempan TA, Kennedy JL. Search for unstable DNA in schizophrenia families with evidence for genetic anticipation. American Journal of Human Genetics. 59: 905-11. PMID 8808607  0.233
2023 Bassett AS, Reuter MS, Malecki S, Silversides C, Oechslin E. Clinically Relevant Genetic Considerations for Patients With Tetralogy of Fallot. Cjc Pediatric and Congenital Heart Disease. 2: 426-439. PMID 38161665 DOI: 10.1016/j.cjcpc.2023.10.002  0.231
2022 Jacquemont S, Huguet G, Klein M, Chawner SJRA, Donald KA, van den Bree MBM, Sebat J, Ledbetter DH, Constantino JN, Earl RK, McDonald-McGinn DM, van Amelsvoort T, Swillen A, O'Donnell-Luria AH, Glahn DC, ... ... Bassett AS, et al. Genes To Mental Health (G2MH): A Framework to Map the Combined Effects of Rare and Common Variants on Dimensions of Cognition and Psychopathology. The American Journal of Psychiatry. 179: 189-203. PMID 35236119 DOI: 10.1176/appi.ajp.2021.21040432  0.228
2011 Logan J, Petrill SA, Flax J, Justice LM, Hou L, Bassett AS, Tallal P, Brzustowicz LM, Bartlett CW. Genetic covariation underlying reading, language and related measures in a sample selected for specific language impairment. Behavior Genetics. 41: 651-9. PMID 21193955 DOI: 10.1007/S10519-010-9435-0  0.224
2018 Reuter MS, Walker S, Thiruvahindrapuram B, Whitney J, Cohn I, Sondheimer N, Yuen RKC, Trost B, Paton TA, Pereira SL, Herbrick JA, Wintle RF, Merico D, Howe J, MacDonald JR, ... ... Bassett AS, et al. The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants. Cmaj : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne. 190: E126-E136. PMID 29431110 DOI: 10.1503/Cmaj.171151  0.217
1991 Erlenmeyer-Kimling L, Adamo U, Bassett A, Squires-Wheeler E, Cornblatt B, Roberts S. The New York high-risk project: Comorbidity of axis I disorders in subjects at high risk for schizophrenia or major affective disorders and in low-risk subjects Schizophrenia Research. 4: 276. DOI: 10.1016/0920-9964(91)90141-D  0.216
1986 Bassett AS, Remick RA, Beiser M, Miles JE, Wilt F. The art of pharmacotherapy in depressed outpatients. Canadian Journal of Psychiatry. Revue Canadienne De Psychiatrie. 31: 852-6. PMID 3802005 DOI: 10.1177/070674378603100912  0.214
2022 Reuter MS, Zech M, Hempel M, Altmüller J, Heung T, Pölsler L, Santer R, Thiele H, Trost B, Kubisch C, Scherer SW, Rudnik-Schöneborn S, Bassett AS, Lessel D. Biallelic PAN2 variants in individuals with a syndromic neurodevelopmental disorder and multiple congenital anomalies. European Journal of Human Genetics : Ejhg. PMID 35304602 DOI: 10.1038/s41431-022-01077-y  0.213
2001 Bowen T, Williams N, Norton N, Spurlock G, Wittekindt OH, Morris-Rosendahl DJ, Williams H, Brzustowicz L, Hoogendoorn B, Zammit S, Jones G, Sanders RD, Jones LA, McCarthy G, Jones S, ... Bassett A, et al. Mutation screening of the KCNN3 gene reveals a rare frameshift mutation. Molecular Psychiatry. 6: 259-60. PMID 11326292 DOI: 10.1038/Sj.Mp.4000128  0.209
2011 Bassett AS. Clinical case rounds in child and adolescent psychiatry: Commentary: Anxiety Disorders and Perceptual Disturbances in Adolescents with 22q11.2 Deletion Syndrome Treated with SSRI: A Case Series Journal of the Canadian Academy of Child and Adolescent Psychiatry. 20: 311.  0.206
2020 Stahel P, Nahmias A, Sud SK, Lee SJ, Pucci A, Yousseif A, Youseff A, Jackson T, Urbach DR, Okrainec A, Allard JP, Sockalingam S, Yao T, Barua M, Jiao H, ... ... Bassett AS, et al. Erratum. Evaluation of the Genetic Association Between Adult Obesity and Neuropsychiatric Disease. Diabetes 2019;68:2235-2246. Diabetes. PMID 32086293 DOI: 10.2337/Db20-Er04C  0.205
2023 Ying S, Heung T, Thiruvahindrapuram B, Engchuan W, Yin Y, Blagojevic C, Zhang Z, Hegele RA, Yuen RKC, Bassett AS. Polygenic risk for triglyceride levels in the presence of a high impact rare variant. Bmc Medical Genomics. 16: 281. PMID 37940981 DOI: 10.1186/s12920-023-01717-2  0.2
2016 Buijs PC, Boot E, Shugar A, Fung WL, Bassett AS. Internet Safety Issues for Adolescents and Adults with Intellectual Disabilities. Journal of Applied Research in Intellectual Disabilities : Jarid. PMID 26914835 DOI: 10.1111/Jar.12250  0.197
2010 Ott J, Wang X, Elston RC, Zhu X, Kremeyer B, García J, Müller H, Burley MW, Herzberg I, Parra MV, Duque C, Vega J, Montoya P, López MC, Bedoya G, ... ... Bassett AS, et al. Subject Index Vol. 70, 2010 Human Heredity. 70: 303-303. DOI: 10.1159/000324573  0.189
2002 Dempfle A, Hinney A, Hebebrand J, Schäfer H, Bauerfeind A, Knoblauch H, Schuster H, Luft FC, Reich JG, Malley JD, Naiman DQ, Bailey-Wilson JE, Nothnagel M, Fürst R, Rohde K, ... ... Bassett AS, et al. Subject Index Vol. 54, 2002 Human Heredity. 54: 220. DOI: 10.1159/000071494  0.189
2024 Malecki SL, Heung T, Wodchis WP, Saskin R, Palma L, Verma AA, Bassett AS. Young adults with a 22q11.2 microdeletion and the cost of aging with complexity in a population-based context. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 101088. PMID 38310401 DOI: 10.1016/j.gim.2024.101088  0.183
1993 Squires-Wheeler E, Skodol AE, Adamo UH, Bassett AS, Gewirtz GR, Honer WG, Cornblatt BA, Roberts SA, Erlenmeyer-Kimling L. PERSONALITY FEATURES AND DISORDER IN THE SUBJECTS IN THE NEW YORK HIGH-RISK PROJECT. Journal of Psychiatric Research. 27: 379-393. PMID 22287799 DOI: 10.1016/0022-3956(93)90065-A  0.18
2021 Reuter MS, Chaturvedi RR, Jobling RK, Pellecchia G, Hamdan O, Sung WWL, Nalpathamkalam T, Attaluri P, Silversides CK, Wald RM, Marshall CR, Williams S, Keavney BD, Thiruvahindrapuram B, Scherer SW, ... Bassett AS, et al. Clinical Genetic Risk Variants Inform a Functional Protein Interaction Network for Tetralogy of Fallot. Circulation. Genomic and Precision Medicine. PMID 34328347 DOI: 10.1161/CIRCGEN.121.003410  0.179
2021 Audain E, Wilsdon A, Breckpot J, Izarzugaza JM, Fitzgerald TW, Kahlert AK, Sifrim A, Wünnemann F, Perez-Riverol Y, Abdul-Khaliq H, Bak M, Bassett AS, Benson WD, Berger F, Daehnert I, et al. Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease. Plos Genetics. 17: e1009679. PMID 34324492 DOI: 10.1371/journal.pgen.1009679  0.179
2020 Manshaei R, Merico D, Reuter MS, Engchuan W, Mojarad BA, Chaturvedi R, Heung T, Pellecchia G, Zarrei M, Nalpathamkalam T, Khan R, Okello JBA, Liston E, Curtis M, Yuen RKC, ... ... Bassett AS, et al. Genes and Pathways Implicated in Tetralogy of Fallot Revealed by Ultra-Rare Variant Burden Analysis in 231 Genome Sequences. Frontiers in Genetics. 11: 957. PMID 33110418 DOI: 10.3389/fgene.2020.00957  0.179
2007 Colella S, Yau C, Taylor JM, Mirza G, Butler H, Clouston P, Bassett AS, Seller A, Holmes CC, Ragoussis J. QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data. Nucleic Acids Research. 35: 2013-25. PMID 17341461 DOI: 10.1093/nar/gkm076  0.175
2023 Rong M, Benke T, Zulfiqar Ali Q, Aledo-Serrano Á, Bayat A, Rossi A, Devinsky O, Qaiser F, Ali AS, Fasano A, Bassett AS, Andrade DM. Adult Phenotype of -DEE. Neurology. Genetics. 9: e200105. PMID 38045990 DOI: 10.1212/NXG.0000000000200105  0.172
2011 Ott J, Wang X, Elston RC, Zhu X, Kremeyer B, García J, Müller H, Burley MW, Herzberg I, Parra MV, Duque C, Vega J, Montoya P, López MC, Bedoya G, ... ... Bassett AS, et al. Contents Vol. 70, 2010 Human Heredity. 70. DOI: 10.1159/000324574  0.169
2002 Dempfle A, Hinney A, Hebebrand J, Schäfer H, Bauerfeind A, Knoblauch H, Schuster H, Luft FC, Reich JG, Malley JD, Naiman DQ, Bailey-Wilson JE, Nothnagel M, Fürst R, Rohde K, ... ... Bassett AS, et al. Contents Vol. 54, 2002 Human Heredity. 54: 221. DOI: 10.1159/000071492  0.169
1996 Correia S, Chow E, Weksberg R, McAlduff J, Bomba M, Scutt L, Chen M, Hodgkinson K, Honer WG, Jones C, Beatty B, Squire J, Bassett AS. Velocardiofacial syndrome (VCFS) in a random schizophrenic sample Psychiatric Genetics. 6: 167. DOI: 10.1097/00041444-199623000-00087  0.169
2013 Hodgkinson KA, Connors SP, Merner N, Haywood A, Young TL, McKenna WJ, Gallagher B, Curtis F, Bassett AS, Parfrey PS. The natural history of a genetic subtype of arrhythmogenic right ventricular cardiomyopathy caused by a p.S358L mutation in TMEM43. Clinical Genetics. 83: 321-31. PMID 22725725 DOI: 10.1111/j.1399-0004.2012.01919.x  0.168
1995 Chow EW, Collins EJ, Nuttall SE, Bassett AS. Clinical use of clozapine in a major urban setting: one year experience. Journal of Psychiatry & Neuroscience : Jpn. 20: 133-40. PMID 7703222  0.161
2003 Dempfle A, Hinney A, Hebebrand J, Schäfer H, Bauerfeind A, Knoblauch H, Schuster H, Luft FC, Reich JG, Malley JD, Naiman DQ, Bailey-Wilson JE, Nothnagel M, Fürst R, Rohde K, ... ... Bassett AS, et al. Tribute to Lodewijk Sandkuijl Human Heredity. 54: 165. DOI: 10.1159/000071490  0.156
1991 Bassett A, Hilldoff Adamo U, Squires-Wheeler E, Cornblatt B, Erlenmeyer-Kimling L. Onset and premorbid clinical features of psychosis in the New York high-risk project Schizophrenia Research. 4: 273-274. DOI: 10.1016/0920-9964(91)90136-F  0.134
2021 Audain E, Wilsdon A, Breckpot J, Izarzugaza JMG, Fitzgerald TW, Kahlert AK, Sifrim A, Wünnemann F, Perez-Riverol Y, Abdul-Khaliq H, Bak M, Bassett AS, Benson DW, Berger F, Daehnert I, et al. Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease. Plos Genetics. 17: e1009809. PMID 34547032 DOI: 10.1371/journal.pgen.1009809  0.127
1993 Berg D, Bassett AS. Darier's disease: current understanding of pathogenesis and future role of genetic studies. International Journal of Dermatology. 32: 397-400. PMID 8320017  0.122
1993 Bassett A, Nuttall S, Bury A, Roy R, McAlduff J, Honer W. Influence of positive and negative symptoms and thought disorder on mini-mental state examination scores Schizophrenia Research. 9: 92. DOI: 10.1016/0920-9964(93)90087-Y  0.117
2005 Hodgkinson KA, Parfrey PS, Bassett AS, Kupprion C, Drenckhahn J, Norman MW, Thierfelder L, Stuckless SN, Dicks EL, McKenna WJ, Connors SP. The impact of implantable cardioverter-defibrillator therapy on survival in autosomal-dominant arrhythmogenic right ventricular cardiomyopathy (ARVD5). Journal of the American College of Cardiology. 45: 400-8. PMID 15680719 DOI: 10.1016/J.Jacc.2004.08.068  0.11
1991 Cornblatt B, Hilldoff Adamo U, Obuchowski M, Bassett A, Squires-Wheeler E, Erlenmeyer-Kimling L. The New York high-risk project: History of study, overview of marker findings to date and prevalence of axis I high and low risk subjects Schizophrenia Research. 4: 275. DOI: 10.1016/0920-9964(91)90139-I  0.1
2023 Ying S, Heung T, Thiruvahindrapuram B, Engchuan W, Yin Y, Blagojevic C, Zhang Z, Hegele RA, Yuen RKC, Bassett AS. Correction: Polygenic risk for triglyceride levels in the presence of a high impact rare variant. Bmc Medical Genomics. 16: 302. PMID 37996907 DOI: 10.1186/s12920-023-01742-1  0.099
2023 White LK, Crowley TB, Finucane B, McClellan EJ, Donoghue S, Garcia-Minaur S, Repetto GM, Fischer M, Jacquemont S, Gur RE, Maillard AM, Donald KA, Bassett AS, Swillen A, McDonald-McGinn DM. Gathering the Stakeholder's Perspective: Experiences and Opportunities in Rare Genetic Disease Research. Genes. 14. PMID 36672911 DOI: 10.3390/genes14010169  0.094
2000 Chow E, Desai H, Selhi Z, Bassett A, Collins E. A study to evaluate the antiaggressive properties of clozapine Schizophrenia Research. 41: 183. DOI: 10.1016/S0920-9964(00)90745-X  0.072
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