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



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, Steven J Lubbe, Caroline H Williams-Gray, Roger A Barker, Karin D van Dijk, Henk W Berendse, Peter Heutink, Jean-Christophe Corvol, Florence Cormier, Suzanne Lesage, Alexis Brice, Kathrin Brockmann, Claudia Schulte, Thomas Gasser, Thomas Foltynie, Patricia Limousin, Karen E Morrison, Carl E Clarke, Stephen Sawcer, Tom T Warner, Andrew J Lees, Huw R Morris, Mike A Nalls, Andrew B Singleton, John Hardy, Andrey Y Abramov, Vincent Plagnol, Nigel M Williams, Nicholas W Wood. Lancet Neurol 2016
Times Cited: 49




List of shared articles



Times cited

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

Age-Related Parkinsonian Signs in Microdeletion 22q11.2.
Erik Boot, Thierry Q Mentzel, Lisa D Palmer, Peter N van Harten, Connie Marras, Anthony E Lang, Anne S Bassett. Mov Disord 2020
0

Neurobiological perspective of 22q11.2 deletion syndrome.
Janneke R Zinkstok, Erik Boot, Anne S Bassett, Noboru Hiroi, Nancy J Butcher, Claudia Vingerhoets, Jacob A S Vorstman, Therese A M J van Amelsvoort. Lancet Psychiatry 2019
23

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

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

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

Update on the 22q11.2 deletion syndrome and its relevance to schizophrenia.
Lily Van, Erik Boot, Anne S Bassett. Curr Opin Psychiatry 2017
42

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

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


Genomic Disorders in Psychiatry-What Does the Clinician Need to Know?
Chelsea Lowther, Gregory Costain, Danielle A Baribeau, Anne S Bassett. Curr Psychiatry Rep 2017
19

Copy Number Variation in Syndromic Forms of Psychiatric Illness: The Emerging Value of Clinical Genetic Testing in Psychiatry.
Christian G Bouwkamp, Anneke J A Kievit, Sander Markx, Joseph I Friedman, Laura van Zutven, Rick van Minkelen, Terry Vrijenhoek, Bin Xu, Ineke Sterrenburg-van de Nieuwegiessen, Joris A Veltman,[...]. Am J Psychiatry 2017
9