Anne S. Bassett - Publications, H-index & Citations

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Anne S. Bassett

ku leuven

73H-index

336Paper Count

2.1WCitation Count

Published Papers 177

Publication Date

Genome-wide tandem repeat expansions modify schizophrenia risk in the presence of a 22q11.2 deletion

Molecular Psychiatry

IF10.1

2026-04-15

OAAI

Muyang Cheng; Yue Yin; Worrawat Engchuan; Tracy Heung; Bernice E. Morrow; Anne S. Bassett; Ryan K. C. Yuen

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Adult outcomes of clinically relevant genomic disorders: A systematic review and meta-analysis

Genetics in Medicine

IF6.2

2026-01-15

OAAI

Sarah L. Malecki; David DArienzo; Erica Wennberg; Emily Ana Butler; Nimit Vediya; Manav V. Vyas; Vanda McNiven; Jessie Cunningham; Therese A. Stukel; Amol A. Verma; Eyal Cohen; Anne S. Bassett

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Movement Disorders Associated with 22q11.2 Microdeletion: A Scoping Review

MOVEMENT DISORDERS CLINICAL PRACTICE

IF2.7

2025-12-01

OAAI

Reyes, Nikolai Gil D.; Di Luca, Daniel G.; Marras, Connie; Boot, Erik; Yuen, Ryan K. C.; Lang, Anthony E.; Bassett, Anne S.

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Prevalence and Spectrum of Congenital Heart Disease in Individuals With Distal Chromosome 22q11.22-23 Deletions

Clinical Genetics

IF2.3

2025-12-01

OAAI

Nelson, Tanner J.; McGinn, Daniel E.; Crowley, T. Blaine; Rockart, Lydia; Green, Audrey; Giunta, Victoria; Tran, Oanh; Miller, Daniella; Breckpot, Jeroen; Swillen, Ann; Digilio, M. Cristina; Unolt, Marta; Putotto, Carolina; Pulvirenti, Federica; Marino, Bruno; Emanuel, Beverly S.; Zackai, Elaine H.; Zhang, Zhengdong D.; Goldmuntz, Elizabeth; Boot, Erik; Bassett, Anne S.; Morrow, Bernice E.; McDonald-McGinn, Donna M.

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The importance of intrafamilial cognitive phenotyping by the case of 22q11.2 deletion, 15q11.2 deletion, and families with inherited copy number variants of unknown significance

Journal of Neurodevelopmental Disorders

IF4

2025-11-28

OAAI

Elise Pelgrims; Laurens Hannes; Ilse Noens; Yoni Peeters; Hilde Peeters; Ania M. Fiksinski; Tracy Heung; Anne S. Bassett; Jeroen Breckpot; Ann Swillen

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Single cell RNA-seq analysis of hematopoietic cell types in 22q11.2 deletion syndrome reveals significant changes to non-T cells

Pediatric Allergy and Immunology

IF4.5

2025-11-01

PREAI

Beigel Katherine; Alsaati Nouf; Kelly Maurer; Donna McDonald-McGinn; T. Blaine Crowley; Montana Knight; Sarah E. Henrickson; Anne Bassett; Kathleen E. Sullivan

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Autoantibodies in patients with 22q11.2 deletion syndrome and psychosis

Journal of Allergy and Clinical Immunology

IF11.2

2025-07-28

PREAI

Samantha Y. Starkey; Kelly Maurer; Anne Bassett; Donna M. McDonald McGinn; Kathleen E. Sullivan

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Comment Closing gaps in care and knowledge for adults with complex genetic conditions

CANADIAN MEDICAL ASSOCIATION JOURNAL

IF11.3

2025-02-09

OAAI

Malecki, Sarah; Cohen, Eyal; Verma, Amol A.; Bassett, Anne S.

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Real-World Treatment of Schizophrenia in Adults With a 22q11.2 Microdeletion

CANADIAN JOURNAL OF PSYCHIATRY-REVUE CANADIENNE DE PSYCHIATRIE

IF3.8

2024-12-06

PREAI

Van, Lily; Heung, Tracy; Reyes, Nikolai Gil D.; Boot, Erik; Chow, Eva W. C.; Corral, Maria; Bassett, Anne S.

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Adult Phenotype of CHD2-Associated Disorders

NEUROLOGY-GENETICS

IF3.7

2024-12-01

PREAI

Rong, Marlene; Ali, Quratulain Zulfiqar; Aledo-Serrano, Angel; Bayat, Allan; Devinsky, Orrin; Qaiser, Farah; Chandran, Ilakkiah; Ali, Anum; Fasano, Alfonso; Bassett, Anne S.; Andrade, Danielle M.

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Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplications

MOLECULAR PSYCHIATRY

IF10.1

2024-07-24

OAAI

Gur, Ruben C.; Bearden, Carrie E.; Jacquemont, Sebastien; Swillen, Ann; van Amelsvoort, Therese; van den Bree, Marianne; Vorstman, Jacob; Sebat, Jonathan; Ruparel, Kosha; Gallagher, Robert Sean; Mcclellan, Emily; White, Lauren; Crowley, Terrence Blaine; Giunta, Victoria; Kushan, Leila; O'Hora, Kathleen; Verbesselt, Jente; Vandensande, Ans; Vingerhoets, Claudia; van Haelst, Mieke; Hall, Jessica; Harwood, Janet; Chawner, Samuel J. R. A.; Patel, Nishi; Palad, Katrina; Hong, Oanh; Guevara, James; Martin, Charles Olivier; Jizi, Khadije; Belanger, Anne-Marie; Scherer, Stephen W.; Bassett, Anne S.; McDonald-McGinn, Donna M.; Gur, Raquel E.

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The mental health and traumatic experiences of mothers of children with 22q11DS

EUROPEAN JOURNAL OF PSYCHOTRAUMATOLOGY

IF4.1

2024-05-23

OAAI

Finless, Alexandra; Rideout, Andrea L.; Xiong, Ting; Carbyn, Holly; Lingley-Pottie, Patricia; Palmer, Lisa D.; Shugar, Andrea; McDonald-McGinn, Donna M.; McGrath, Patrick J.; Bassett, Anne S.; Cytrynbaum, Cheryl; Orr, Matt; Swillen, Ann; Meier, Sandra

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Expanding the phenotypic spectrum of NOTCH1 variants: clinical manifestations in families with congenital heart disease

EUROPEAN JOURNAL OF HUMAN GENETICS

IF4.6

2024-05-22

OAAI

Stanley, Kaitlin J.; Kalbfleisch, Kelsey J.; Moran, Olivia M.; Chaturvedi, Rajiv R.; Roifman, Maian; Chen, Xin; Manshaei, Roozbeh; Martin, Nicole; McDermott, Simina; McNiven, Vanda; Myles-Reid, Diane; Nield, Lynne E.; Reuter, Miriam S.; Schwartz, Marci L. B.; Shannon, Patrick; Silver, Rachel; Somerville, Cherith; Teitelbaum, Ronni; Zahavich, Laura; Bassett, Anne S.; Kim, Raymond H.; Mital, Seema; Chitayat, David; Jobling, Rebekah K.

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Young adults with a 22q11.2 microdeletion and the cost of aging with complexity in a population-based context

GENETICS IN MEDICINE

IF6.2

2024-05-01

OAAI

Malecki, Sarah L.; Heung, Tracy; Wodchis, Walter P.; Saskin, Refi; Palma, Luis; Verma, Amol A.; Bassett, Anne S.

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Source-based morphometry reveals structural brain pattern abnormalities in 22q11.2 deletion syndrome

HUMAN BRAIN MAPPING

IF3.3

2024-01-12

OAAI

Ge, Ruiyang; Ching, Christopher R. K.; Bassett, Anne S.; Kushan, Leila; Antshel, Kevin M.; van Amelsvoort, Therese; Bakker, Geor; Butcher, Nancy J.; Campbell, Linda E.; Chow, Eva W. C.; Craig, Michael; Crossley, Nicolas A.; Cunningham, Adam; Daly, Eileen; Doherty, Joanne L.; Durdle, Courtney A.; Emanuel, Beverly S.; Fiksinski, Ania; Forsyth, Jennifer K.; Fremont, Wanda; Goodrich-Hunsaker, Naomi J.; Gudbrandsen, Maria; Gur, Raquel E.; Jalbrzikowski, Maria; Kates, Wendy R.; Lin, Amy; Linden, David E. J.; Mccabe, Kathryn L.; McDonald-McGinn, Donna; Moss, Hayley; Murphy, Declan G.; Murphy, Kieran C.; Owen, Michael J.; Villalon-Reina, Julio E.; Repetto, Gabriela M.; Roalf, David R.; Ruparel, Kosha; Schmitt, J. Eric; Schuite-Koops, Sanne; Angkustsiri, Kathleen; Sun, Daqiang; Vajdi, Ariana; van den Bree, Marianne; Vorstman, Jacob; Thompson, Paul M.; Vila-Rodriguez, Fidel; Bearden, Carrie E.

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Adult Phenotype of SYNGAP1-DEE

NEUROLOGY-GENETICS

IF3.7

2023-12-01

OAAI

Rong, Marlene; Benke, Tim; Ali, Quratulain Zulfiqar; Aledo-Serrano, Angel; Bayat, Allan; Rossi, Alessandra; Devinsky, Orrin; Qaiser, Farah; Ali, Anum S.; Fasano, Alfonso; Bassett, Anne S.; Andrade, Danielle M.

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Approaches to studying the impact of 22q11.2 copy number variants

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2023-07-01

OAAI

Bassett, Anne S.; McDonald-McGinn, Donna M.; Boot, Erik; Oskarsdottir, Solveig; Yuen, Ryan K. C.

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Adult-onset obstructive sleep apnea and pediatric pharyngoplasty in 22q11.2 deletion syndrome

SLEEP MEDICINE

IF3.4

2023-04-01

OAAI

Cancelliere, Sabrina; Heung, Tracy; Fischbach, Simone; Klaiman, Paula; Bassett, Anne S.

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Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia

MOLECULAR PSYCHIATRY

IF10.1

2023-03-03

PREAI

Lin, Jhih-Rong; Zhao, Yingjie; Jabalameli, M. Reza; Nguyen, Nha; Mitra, Joydeep; Swillen, Ann; Vorstman, Jacob A. S.; Chow, Eva W. C.; van den Bree, Marianne; Emanuel, Beverly S.; Vermeesch, Joris R.; Owen, Michael J.; Williams, Nigel M.; Bassett, Anne S.; McDonald-McGinn, Donna M.; Gur, Raquel E.; Bearden, Carrie E.; Morrow, Bernice E.; Lachman, Herbert M.; Zhang, Zhengdong D.

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Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndrome

GENETICS IN MEDICINE

IF6.2

2023-03-01

OAAI

Boot, Erik; Oskarsdottir, Solveig; Loo, Joanne C. Y.; Crowley, Terrence Blaine; Orchanian-Cheff, Ani; Andrade, Danielle M.; Arganbright, Jill M.; Castelein, Rene M.; Cserti-Gazdewich, Christine; de Reuver, Steven; Fiksinski, Ania M.; Klingberg, Gunilla; Lang, Anthony E.; Mascarenhas, Maria R.; Moss, Edward M.; Nowakowska, Beata Anna; Oechslin, Erwin; Palmer, Lisa; Repetto, Gabriela M.; Reyes, Nikolai Gil D.; Schneider, Maude; Silversides, Candice; Sullivan, Kathleen E.; Swillen, Ann; van Amelsvoort, Therese A. M. J.; Van Batavia, Jason P.; Vingerhoets, Claudia; McDonald-McGinn, Donna M.; Bassett, Anne S.

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Research Directions