Anne S. Bassett, M.D. - Publications

Affiliations: 
University of Toronto, Toronto, ON, Canada 

192 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
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  0.48
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  1
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  1
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  1
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  1
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  1
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  1
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  1
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  1
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  0.48
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  0.48
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  1
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  1
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  0.48
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  1
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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.  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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: 10.1016/j.schres.2007.05.040  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
2002 Bassett AS, Chow EW, Weksberg R, Brzustowicz L. Schizophrenia and genetics: new insights. Current Psychiatry Reports. 4: 307-14. PMID 12126600  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
2001 Bassett AS. Psychiatric genetics in the 21st century. Canadian Journal of Psychiatry. Revue Canadienne De Psychiatrie. 46: 121-2. PMID 11280079  0.48
2001 Bassett AS, Chow EWC, Brzustowicz L. The genetics of schizophrenia Neuroscience News. 4: 20-26.  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
1999 Haslam DR, Gardner DM, Oluboka T. Re: Canadian clinical practice guidelines for the treatment of schizophrenia. Canadian Journal of Psychiatry. Revue Canadienne De Psychiatrie. 44: 390-1. PMID 10332581  0.48
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.  0.48
1999 Bassett AS, Chow E, Scltt L, Hüücmmün K, Weksberg R. Adult phenotype of 22q11 deletion syndrome and schizophrenia Genetic Counseling. 10: 111-112.  0.48
1998 Bassett AS. Progress on the genetics of schizophrenia. Journal of Psychiatry & Neuroscience : Jpn. 23: 270-3. PMID 9846030  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
1994 Bassett AS, Honer WG. Evidence for anticipation in schizophrenia. American Journal of Human Genetics. 54: 864-70. PMID 8178826  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
1992 Bassett AS. Chromosomal aberrations and schizophrenia. Autosomes. The British Journal of Psychiatry : the Journal of Mental Science. 161: 323-34. PMID 1393302  0.48
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  0.48
1991 Bassett AS. Linkage analysis of schizophrenia: challenges and promise. Social Biology. 38: 189-96. PMID 1801200  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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  0.48
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