A citation-based method for searching scientific literature


List of co-cited articles
23 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay.
Rachel D Burnside, Romela Pasion, Fady M Mikhail, Andrew J Carroll, Nathaniel H Robin, Erin L Youngs, Inder K Gadi, Elizabeth Keitges, Vikram L Jaswaney, Peter R Papenhausen,[...]. Hum Genet 2011
159
55


The 15q11.2 BP1-BP2 microdeletion syndrome: a review.
Devin M Cox, Merlin G Butler. Int J Mol Sci 2015
94
44

Chromosomal Microarray Analysis of Consecutive Individuals with Autism Spectrum Disorders Using an Ultra-High Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders.
Karen S Ho, E Robert Wassman, Adrianne L Baxter, Charles H Hensel, Megan M Martin, Aparna Prasad, Hope Twede, Rena J Vanzo, Merlin G Butler. Int J Mol Sci 2016
25
33

Molecular genetic classification in Prader-Willi syndrome: a multisite cohort study.
Merlin G Butler, Samantha N Hartin, Waheeda A Hossain, Ann M Manzardo, Virginia Kimonis, Elisabeth Dykens, June Anne Gold, Soo-Jeong Kim, Nicolette Weisensel, Roy Tamura,[...]. J Med Genet 2019
43
33

Parent-of-Origin Effects in 15q11.2 BP1-BP2 Microdeletion (Burnside-Butler) Syndrome.
Kyle W Davis, Moises Serrano, Sara Loddo, Catherine Robinson, Viola Alesi, Bruno Dallapiccola, Antonio Novelli, Merlin G Butler. Int J Mol Sci 2019
9
33

NIPA1 gene mutations cause autosomal dominant hereditary spastic paraplegia (SPG6).
Shirley Rainier, Jing-Hua Chai, Debra Tokarz, Robert D Nicholls, John K Fink. Am J Hum Genet 2003
131
33

Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition.
Dennis van der Meer, Ida E Sønderby, Tobias Kaufmann, G Bragi Walters, Abdel Abdellaoui, David Ames, Katrin Amunts, Micael Andersson, Nicola J Armstrong, Manon Bernard,[...]. JAMA Psychiatry 2020
20
33

Analysis of the Prader-Willi syndrome imprinting center using droplet digital PCR and next-generation whole-exome sequencing.
Samantha N Hartin, Waheeda A Hossain, David Francis, David E Godler, Sangjucta Barkataki, Merlin G Butler. Mol Genet Genomic Med 2019
10
22

Prader-Willi Syndrome: Clinical and Genetic Findings.
Merlin G Butler, Travis Thompson. Endocrinologist 2000
59
22

Prader-Willi-Like Phenotype Caused by an Atypical 15q11.2 Microdeletion.
Qiming Tan, Kathryn J Potter, Lisa Cole Burnett, Camila E Orsso, Mark Inman, Davis C Ryman, Andrea M Haqq. Genes (Basel) 2020
11
22

Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy.
S B Cassidy, L W Lai, R P Erickson, L Magnuson, E Thomas, R Gendron, J Herrmann. Am J Hum Genet 1992
145
22



Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.
R D Nicholls, J H Knoll, M G Butler, S Karam, M Lalande. Nature 1989
659
22

Prader-Willi syndrome.
Suzanne B Cassidy, Stuart Schwartz, Jennifer L Miller, Daniel J Driscoll. Genet Med 2012
598
22

Clinical and genetic aspects of Angelman syndrome.
Charles A Williams, Daniel J Driscoll, Aditi I Dagli. Genet Med 2010
154
22

Methylation-specific multiplex ligation-dependent probe amplification and identification of deletion genetic subtypes in Prader-Willi syndrome.
Rebecca S Henkhaus, Soo-Jeong Kim, Virginia E Kimonis, June-Anne Gold, Elisabeth M Dykens, Daniel J Driscoll, Merlin G Butler. Genet Test Mol Biomarkers 2012
23
22

Prader-Willi Syndrome - Clinical Genetics, Diagnosis and Treatment Approaches: An Update.
Merlin G Butler, Jennifer L Miller, Janice L Forster. Curr Pediatr Rev 2019
35
22


Estimating the effect size of the 15Q11.2 BP1-BP2 deletion and its contribution to neurodevelopmental symptoms: recommendations for practice.
Aia Elise Jønch, Elise Douard, Clara Moreau, Anke Van Dijck, Marzia Passeggeri, Frank Kooy, Jacques Puechberty, Carolyn Campbell, Damien Sanlaville, Henrietta Lefroy,[...]. J Med Genet 2019
14
22

CNVs conferring risk of autism or schizophrenia affect cognition in controls.
Hreinn Stefansson, Andreas Meyer-Lindenberg, Stacy Steinberg, Brynja Magnusdottir, Katrin Morgen, Sunna Arnarsdottir, Gyda Bjornsdottir, G Bragi Walters, Gudrun A Jonsdottir, Orla M Doyle,[...]. Nature 2014
371
22

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
22

Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders.
Daniel J Weiner, Emilie M Wigdor, Stephan Ripke, Raymond K Walters, Jack A Kosmicki, Jakob Grove, Kaitlin E Samocha, Jacqueline I Goldstein, Aysu Okbay, Jonas Bybjerg-Grauholm,[...]. Nat Genet 2017
182
11

Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants.
Lucilla Pizzo, Matthew Jensen, Andrew Polyak, Jill A Rosenfeld, Katrin Mannik, Arjun Krishnan, Elizabeth McCready, Olivier Pichon, Cedric Le Caignec, Anke Van Dijck,[...]. Genet Med 2019
53
11

A randomized double-blind study of atomoxetine versus placebo for attention-deficit/hyperactivity disorder symptoms in children with autism spectrum disorder.
Myriam Harfterkamp, Gigi van de Loo-Neus, Ruud B Minderaa, Rutger-Jan van der Gaag, Rodrigo Escobar, Alexander Schacht, Sireesha Pamulapati, Jan K Buitelaar, Pieter J Hoekstra. J Am Acad Child Adolesc Psychiatry 2012
73
11

Contactins in the central nervous system: role in health and disease.
Madhurima Chatterjee, Detlev Schild, Charlotte E Teunissen. Neural Regen Res 2019
21
11

A genome-wide linkage study of autism spectrum disorder and the broad autism phenotype in extended pedigrees.
Marc Woodbury-Smith, Andrew D Paterson, Irene O'Connor, Mehdi Zarrei, Ryan K C Yuen, Jennifer L Howe, Ann Thompson, Morgan Parlier, Bridget Fernandez, Joseph Piven,[...]. J Neurodev Disord 2018
7
14

Clinical genetic testing for patients with autism spectrum disorders.
Yiping Shen, Kira A Dies, Ingrid A Holm, Carolyn Bridgemohan, Magdi M Sobeih, Elizabeth B Caronna, Karen J Miller, Jean A Frazier, Iris Silverstein, Jonathan Picker,[...]. Pediatrics 2010
241
11

A randomized controlled study of parent-assisted Children's Friendship Training with children having autism spectrum disorders.
Fred Frankel, Robert Myatt, Catherine Sugar, Cynthia Whitham, Clarissa M Gorospe, Elizabeth Laugeson. J Autism Dev Disord 2010
84
11


Assessment and treatment in autism spectrum disorders: a focus on genetics and psychiatry.
Merlin G Butler, Erin L Youngs, Jennifer L Roberts, Jessica A Hellings. Autism Res Treat 2012
9
11

Psychopharmacological interventions in autism spectrum disorder.
Robert E Accordino, Christen Kidd, Laura C Politte, Charles A Henry, Christopher J McDougle. Expert Opin Pharmacother 2016
37
11

Management of Sleep Disorders in Children With Neurodevelopmental Disorders: A Review.
Allison Beck Blackmer, James A Feinstein. Pharmacotherapy 2016
70
11

Increased grey matter volume of the right superior temporal gyrus in healthy children with autistic cognitive style: A VBM study.
Akiko Kobayashi, Susumu Yokota, Hikaru Takeuchi, Kohei Asano, Michiko Asano, Yuko Sassa, Yasuyuki Taki, Ryuta Kawashima. Brain Cogn 2020
3
33

Extended-Release Guanfacine for Hyperactivity in Children With Autism Spectrum Disorder.
Lawrence Scahill, James T McCracken, Bryan H King, Carol Rockhill, Bhavik Shah, Laura Politte, Roy Sanders, Mendy Minjarez, Jennifer Cowen, Jennifer Mullett,[...]. Am J Psychiatry 2015
70
11


Use of clonidine in children with autism spectrum disorders.
Xue Ming, Emily Gordon, Ning Kang, George C Wagner. Brain Dev 2008
74
11

Pharmacogenetics and Psychiatric Care: A Review and Commentary.
Merlin G Butler. J Ment Health Clin Psychol 2018
5
20

A double-blind, placebo-controlled study of valproate for aggression in youth with pervasive developmental disorders.
Jessica A Hellings, Marilyn Weckbaugh, Elizabeth J Nickel, Sharon E Cain, Jennifer R Zarcone, R Matthew Reese, Sandra Hall, David J Ermer, Luke Y Tsai, Stephen R Schroeder,[...]. J Child Adolesc Psychopharmacol 2005
86
11

Mitochondrial genes and disease.
D C Wallace. Hosp Pract (Off Ed) 1986
43
11

Functional and structural MR imaging in neuropsychiatric disorders, part 2: application in schizophrenia and autism.
S Mueller, D Keeser, M F Reiser, S Teipel, T Meindl. AJNR Am J Neuroradiol 2012
34
11

Pharmacogenetics and pharmacogenomics: development, science, and translation.
Richard M Weinshilboum, Liewei Wang. Annu Rev Genomics Hum Genet 2006
101
11

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.
Dalila Pinto, Elsa Delaby, Daniele Merico, Mafalda Barbosa, Alison Merikangas, Lambertus Klei, Bhooma Thiruvahindrapuram, Xiao Xu, Robert Ziman, Zhuozhi Wang,[...]. Am J Hum Genet 2014
516
11

Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations.
M G Butler, M J Dasouki, X-P Zhou, Z Talebizadeh, M Brown, T N Takahashi, J H Miles, C H Wang, R Stratton, R Pilarski,[...]. J Med Genet 2005
494
11



Genetic heritability and shared environmental factors among twin pairs with autism.
Joachim Hallmayer, Sue Cleveland, Andrea Torres, Jennifer Phillips, Brianne Cohen, Tiffany Torigoe, Janet Miller, Angie Fedele, Jack Collins, Karen Smith,[...]. Arch Gen Psychiatry 2011
971
11


Treatment of anxiety in autism spectrum disorders using cognitive behaviour therapy: A systematic review.
Russell Lang, April Regester, Stacy Lauderdale, Kristen Ashbaugh, Anna Haring. Dev Neurorehabil 2010
75
11


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.