A citation-based method for searching scientific literature

Wai Lun Alan Fung, Nancy J Butcher, Gregory Costain, Danielle M Andrade, Erik Boot, Eva W C Chow, Brian Chung, Cheryl Cytrynbaum, Hanna Faghfoury, Leona Fishman, Sixto García-Miñaúr, Susan George, Anthony E Lang, Gabriela Repetto, Andrea Shugar, Candice Silversides, Ann Swillen, Therese van Amelsvoort, Donna M McDonald-McGinn, Anne S Bassett. Genet Med 2015
Times Cited: 114



Anne S Bassett, Donna M McDonald-McGinn, Koen Devriendt, Maria Cristina Digilio, Paula Goldenberg, Alex Habel, Bruno Marino, Solveig Oskarsdottir, Nicole Philip, Kathleen Sullivan, Ann Swillen, Jacob Vorstman. J Pediatr 2011
Times Cited: 294




List of shared articles



Times cited

Inborn errors of thymic stromal cell development and function.
Alexandra Y Kreins, Stefano Maio, Fatima Dhalla. Semin Immunopathol 2021
2

Clinical evaluation of patients with a neuropsychiatric risk copy number variant.
Samuel Jra Chawner, Cameron J Watson, Michael J Owen. Curr Opin Genet Dev 2021
0

A normative chart for cognitive development in a genetically selected population.
Ania M Fiksinski, Carrie E Bearden, Anne S Bassett, Rene S Kahn, Janneke R Zinkstok, Stephen R Hooper, Wanda Tempelaar, Jacob A S Vorstman, Elemi J Breetvelt. Neuropsychopharmacology 2021
1


Resilience and quality of life in young adults with a 22q11.2 deletion syndrome: a patient's perspective.
Kris Van de Woestyne, Ans Vandensande, Kristof Vansteelandt, Bea Maes, Elfi Vergaelen, Ann Swillen. Eur Child Adolesc Psychiatry 2021
0

Distinct immune trajectories in patients with chromosome 22q11.2 deletion syndrome and immune-mediated diseases.
T Blaine Crowley, Ian M Campbell, Emily J Liebling, Michele P Lambert, Lorraine E Levitt Katz, Jennifer Heimall, Alice Bailey, Daniel E McGinn, Donna M McDonald McGinn, Kathleen E Sullivan. J Allergy Clin Immunol 2021
0

How does genetic variation modify ND-CNV phenotypes?
Thomas J Dinneen, Fiana Ní Ghrálaigh, Ruth Walsh, Lorna M Lopez, Louise Gallagher. Trends Genet 2021
0

Medical, welfare, and educational challenges and psychological distress in parents caring for an individual with 22q11.2 deletion syndrome: A cross-sectional survey in Japan.
Ryo Morishima, Yousuke Kumakura, Satoshi Usami, Akiko Kanehara, Miho Tanaka, Noriko Okochi, Naomi Nakajima, Junko Hamada, Tomoko Ogawa, Shuntaro Ando,[...]. Am J Med Genet A 2021
0

Effectiveness and side effects of psychopharmacotherapy in individuals with 22q11.2 deletion syndrome with comorbid psychiatric disorders: a systematic review.
Mariela Mosheva, Liran Korotkin, Raquel E Gur, Abraham Weizman, Doron Gothelf. Eur Child Adolesc Psychiatry 2020
7


Access to Multidisciplinary Care for Patients With 22q11.2 Deletion Syndrome: Identifying Breakdowns in the Screening Process.
Amjed Abu-Ghname, Aurelia T Perdanasari, Sarth Raj, Jain Seema, Kristina D Wilson, Renata S Maricevich. J Craniofac Surg 2020
0

The Genetics and Epigenetics of 22q11.2 Deletion Syndrome.
Qiumei Du, M Teresa de la Morena, Nicolai S C van Oers. Front Genet 2020
19


Relationship between parent-reported gastrointestinal symptoms, sleep problems, autism spectrum disorder symptoms, and behavior problems in children and adolescents with 22q11.2 deletion syndrome.
Geraldine Leader, Maeve Murray, Páraic S O'Súilleabháin, Leanne Maher, Katie Naughton, Sophia Arndt, Keeley White, Ivan Traina, Arlene Mannion. Res Dev Disabil 2020
1

Prenatal screening of DiGeorge (22q11.2 deletion) syndrome by abnormalities of the great arteries among Thai pregnant women.
Kuntharee Traisrisilp, Fuanglada Tongprasert, Kasemsri Srisupundit, Suchaya Luewan, Theera Tongsong. Obstet Gynecol Sci 2020
2

High Rates of Genetic Diagnosis in Psychiatric Patients with and without Neurodevelopmental Disorders: Toward Improved Genetic Diagnosis in Psychiatric Populations.
Joyce So, Venuja Sriretnakumar, Jessica Suddaby, Brianna Barsanti-Innes, Hanna Faghfoury, Timothy Gofine. Can J Psychiatry 2020
0

Cognitive behavioral therapy in 22q11.2 deletion syndrome: A case study of two young adults with an anxiety disorder.
Petra Cm Buijs, Anne S Bassett, David A Gold, Erik Boot. J Intellect Disabil 2020
0

Impact of Interdisciplinary Team Care for Children With 22q11.2 Deletion Syndrome.
Scott E Hickey, Brian Kellogg, Meghan O'Brien, Courtney Hall, Richard E Kirschner, Stephanie L Santoro, Hayley Leonard, Adriane L Baylis. Cleft Palate Craniofac J 2020
2


Lower cortisol levels and attenuated cortisol reactivity to daily-life stressors in adults with 22q11.2 deletion syndrome.
Esther D A van Duin, Thomas Vaessen, Zuzana Kasanova, Wolfgang Viechtbauer, Ulrich Reininghaus, Peter Saalbrink, Claudia Vingerhoets, Dennis Hernaus, Jan Booij, Ann Swillen,[...]. Psychoneuroendocrinology 2019
4

Speech-Language Disorders in 22q11.2 Deletion Syndrome: Best Practices for Diagnosis and Management.
Cynthia B Solot, Debbie Sell, Anne Mayne, Adriane L Baylis, Christina Persson, Oksana Jackson, Donna M McDonald-McGinn. Am J Speech Lang Pathol 2019
10

Adverse effects of antipsychotic medication in patients with 22q11.2 deletion syndrome: A systematic review.
Janna de Boer, Erik Boot, Lissa van Gils, Therese van Amelsvoort, Janneke Zinkstok. Am J Med Genet A 2019
3


Parkinson's disease with hypocalcaemia: adult presentation of 22q11.2 deletion syndrome.
Fradique Moreira, Ana Brás, Joana Ramos Lopes, Cristina Januário. BMJ Case Rep 2018
1

Elucidating the diagnostic odyssey of 22q11.2 deletion syndrome.
Lisa D Palmer, Nancy J Butcher, Erik Boot, Kathleen A Hodgkinson, Tracy Heung, Eva W C Chow, Alina Guna, T Blaine Crowley, Elaine Zackai, Donna M McDonald-McGinn,[...]. Am J Med Genet A 2018
19

Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers.
Marta Unolt, Paolo Versacci, Silvia Anaclerio, Caterina Lambiase, Giulio Calcagni, Matteo Trezzi, Adriano Carotti, Terrence Blaine Crowley, Elaine H Zackai, Elizabeth Goldmuntz,[...]. Am J Med Genet A 2018
17

Neurodevelopmental outcome in 22q11.2 deletion syndrome and management.
Ann Swillen, Edward Moss, Sasja Duijff. Am J Med Genet A 2018
9

Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2.
Erik Boot, Nancy J Butcher, Sean Udow, Connie Marras, Kin Y Mok, Satoshi Kaneko, Matthew J Barrett, Paolo Prontera, Brian D Berman, Mario Masellis,[...]. Neurology 2018
20

Neuropsychiatric expression and catatonia in 22q11.2 deletion syndrome: An overview and case series.
Nancy J Butcher, Erik Boot, Anthony E Lang, Danielle Andrade, Jacob Vorstman, Donna McDonald-McGinn, Anne S Bassett. Am J Med Genet A 2018
10

Understanding the pediatric psychiatric phenotype of 22q11.2 deletion syndrome.
Ania M Fiksinski, Maude Schneider, Clodagh M Murphy, Marco Armando, Stefano Vicari, Jaume M Canyelles, Doron Gothelf, Stephan Eliez, Elemi J Breetvelt, Celso Arango,[...]. Am J Med Genet A 2018
24

22q11.2 deletion syndrome: A tiny piece leading to a big picture.
Donna M McDonald-McGinn. Am J Med Genet A 2018
2

Periventricular nodular heterotopia in 22q11.2 deletion and frontal lobe migration.
Arezoo Rezazadeh, Eduard Bercovici, Tim-Rasmus Kiehl, Eva W Chow, Timo Krings, Anne S Bassett, Danielle M Andrade. Ann Clin Transl Neurol 2018
3

22q11.2 Deletion Syndrome-Associated Parkinson's Disease.
Erik Boot, Anne S Bassett, Connie Marras. Mov Disord Clin Pract 2018
9

Neuropsychiatric aspects of 22q11.2 deletion syndrome: considerations in the prenatal setting.
Anne S Bassett, Gregory Costain, Christian R Marshall. Prenat Diagn 2017
9

Camptodactyly and the 22q11.2 deletion syndrome.
Natario L Couser, Chetna K Pande, Jonathan M Walsh, James Tepperberg, Arthur S Aylsworth. Am J Med Genet A 2017
2

Brain Calcification and Movement Disorders.
Vladimir S Kostić, Igor N Petrović. Curr Neurol Neurosci Rep 2017
13

22q11.2 deletion syndrome in diverse populations.
Paul Kruszka, Yonit A Addissie, Daniel E McGinn, Antonio R Porras, Elijah Biggs, Matthew Share, T Blaine Crowley, Brian H Y Chung, Gary T K Mok, Christopher C Y Mak,[...]. Am J Med Genet A 2017
47

Neuroimaging and clinical features in adults with a 22q11.2 deletion at risk of Parkinson's disease.
Nancy J Butcher, Connie Marras, Margarita Pondal, Pablo Rusjan, Erik Boot, Leigh Christopher, Gabriela M Repetto, Rosemarie Fritsch, Eva W C Chow, Mario Masellis,[...]. Brain 2017
26

Association of airway abnormalities with 22q11.2 deletion syndrome.
Rosalba Sacca, Karen B Zur, T Blaine Crowley, Elaine H Zackai, Kathleen D Valverde, Donna M McDonald-McGinn. Int J Pediatr Otorhinolaryngol 2017
21

Whole-genome sequencing suggests mechanisms for 22q11.2 deletion-associated Parkinson's disease.
Nancy J Butcher, Daniele Merico, Mehdi Zarrei, Lucas Ogura, Christian R Marshall, Eva W C Chow, Anthony E Lang, Stephen W Scherer, Anne S Bassett. PLoS One 2017
11

Neuroradiographic findings in 22q11.2 deletion syndrome.
Lauren A Bohm, Tom C Zhou, Tyler J Mingo, Sarah L Dugan, Richard J Patterson, James D Sidman, Brianne B Roby. Am J Med Genet A 2017
10


Delayed diagnosis of 22q11 deletion syndrome due to late onset hypocalcemia in a 11-year-old girl with imperforated anus.
Dong-Yoon Yoo, Hae Jung Kim, Kee Hyun Cho, Eun Byul Kwon, Eun-Gyong Yoo. Ann Pediatr Endocrinol Metab 2017
4

Treatment of Comorbid Bipolar Disorder Improves Disabilities and Neuropsychological Functioning in DiGeorge Syndrome: A Case Report.
Léa C Perret, Marc-Antoine Lodovighi, Odile Perret, El Chérif Ibrahim, Nicole Philip, Jean-Michel Azorin, Raoul Belzeaux. J Clin Psychopharmacol 2017
1

Pediatric healthcare costs for patients with 22q11.2 deletion syndrome.
Peter Benn, Sushma Iyengar, Terrence Blaine Crowley, Elaine H Zackai, Evanette K Burrows, Solomon Moshkevich, Donna M McDonald-McGinn, Kathleen E Sullivan, Zachary Demko. Mol Genet Genomic Med 2017
3

Fetal growth and gestational factors as predictors of schizophrenia in 22q11.2 deletion syndrome.
Lily Van, Nancy J Butcher, Gregory Costain, Lucas Ogura, Eva W C Chow, Anne S Bassett. Genet Med 2016
19

Communication of Psychiatric Risk in 22q11.2 Deletion Syndrome: A Pilot Project.
Sarah J Hart, Kelly Schoch, Vandana Shashi, Nancy Callanan. J Genet Couns 2016
3


Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data.
Kin Y Mok, Una Sheerin, Javier Simón-Sánchez, Afnan Salaka, Lucy Chester, Valentina Escott-Price, Kiran Mantripragada, Karen M Doherty, Alastair J Noyce, Niccolo E Mencacci,[...]. Lancet Neurol 2016
49