A citation-based method for searching scientific literature

Megan R Glassford, Jill A Rosenfeld, Alexa A Freedman, Michael E Zwick, Jennifer G Mulle. Am J Med Genet A 2016
Times Cited: 39







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



Times Cited
  Times     Co-cited
Similarity


3q29 microdeletion syndrome: clinical and molecular characterization of a new syndrome.
Lionel Willatt, James Cox, John Barber, Elisabet Dachs Cabanas, Amanda Collins, Dian Donnai, David R FitzPatrick, Eddy Maher, Howard Martin, Josep Parnau,[...]. Am J Hum Genet 2005
159
58

Autistic and psychiatric findings associated with the 3q29 microdeletion syndrome: case report and review.
Fabiola Quintero-Rivera, Pantea Sharifi-Hannauer, Julian A Martinez-Agosto. Am J Med Genet A 2010
63
43


Microdeletions of 3q29 confer high risk for schizophrenia.
Jennifer Gladys Mulle, Anne F Dodd, John A McGrath, Paula S Wolyniec, Adele A Mitchell, Amol C Shetty, Nara L Sobreira, David Valle, M Katharine Rudd, Glen Satten,[...]. Am J Hum Genet 2010
158
41


Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication.
Blake C Ballif, Aaron Theisen, Justine Coppinger, Gordon C Gowans, Joseph H Hersh, Suneeta Madan-Khetarpal, Karen R Schmidt, Raymond Tervo, Luis F Escobar, Christopher A Friedrich,[...]. Mol Cytogenet 2008
162
35

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.
Stephan J Sanders, Xin He, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Kaitlin E Samocha, A Ercument Cicek, Michael T Murtha, Vanessa H Bal, Somer L Bishop, Shan Dong,[...]. Neuron 2015
601
33

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.
Christian R Marshall, Daniel P Howrigan, Daniele Merico, Bhooma Thiruvahindrapuram, Wenting Wu, Douglas S Greer, Danny Antaki, Aniket Shetty, Peter A Holmans, Dalila Pinto,[...]. Nat Genet 2017
398
28

Co-occurrence of autism, childhood psychosis, and intellectual disability associated with a de novo 3q29 microdeletion.
Angela Sagar, Jeffrey R Bishop, D Clare Tessman, Steve Guter, Christa L Martin, Edwin H Cook. Am J Med Genet A 2013
31
29

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
23

Study protocol for The Emory 3q29 Project: evaluation of neurodevelopmental, psychiatric, and medical symptoms in 3q29 deletion syndrome.
Melissa M Murphy, T Lindsey Burrell, Joseph F Cubells, Roberto Antonio España, Michael J Gambello, Katrina C B Goines, Cheryl Klaiman, Longchuan Li, Derek M Novacek, Ava Papetti,[...]. BMC Psychiatry 2018
11
81

Neuropsychiatric phenotypes and a distinct constellation of ASD features in 3q29 deletion syndrome: results from the 3q29 registry.
Rebecca M Pollak, Melissa M Murphy, Michael P Epstein, Michael E Zwick, Cheryl Klaiman, Celine A Saulnier, Jennifer G Mulle. Mol Autism 2019
10
90

1.3 Mb de novo deletion in chromosome band 3q29 associated with normal intelligence in a child.
William Cobb, Arne Anderson, Clesson Turner, Ruth D Hoffman, Steven Schonberg, Sondra W Levin. Eur J Med Genet 2010
17
41

3q29 microdeletion syndrome: Cognitive and behavioral phenotype in four patients.
Santina Città, Serafino Buono, Donatella Greco, Concetta Barone, Enrico Alfei, Sara Bulgheroni, Arianna Usilla, Chiara Pantaleoni, Corrado Romano. Am J Med Genet A 2013
12
58

3q29 Microdeletion: a mental retardation disorder unassociated with a recognizable phenotype in two mother-daughter pairs.
Maria Cristina Digilio, Laura Bernardini, Rita Mingarelli, Rossella Capolino, Anna Capalbo, Maria Grazia Giuffrida, Paolo Versacci, Antonio Novelli, Bruno Dallapiccola. Am J Med Genet A 2009
28
25

Familial 3q29 microdeletion syndrome providing further evidence of involvement of the 3q29 region in bipolar disorder.
Jill Clayton-Smith, Carol Giblin, Rupert A Smith, Carolyn Dunn, Lionel Willatt. Clin Dysmorphol 2010
28
25

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein,[...]. Am J Hum Genet 2010
17


3q29 interstitial microdeletion syndrome: an inherited case associated with cardiac defect and normal cognition.
Feng Li, Emily C Lisi, Elizabeth S Wohler, Ada Hamosh, Denise A S Batista. Eur J Med Genet 2009
24
29

A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders.
Flore Zufferey, Elliott H Sherr, Noam D Beckmann, Ellen Hanson, Anne M Maillard, Loyse Hippolyte, Aurélien Macé, Carina Ferrari, Zoltán Kutalik, Joris Andrieux,[...]. J Med Genet 2012
154
15

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.
Maude Schneider, Martin Debbané, Anne S Bassett, Eva W C Chow, Wai Lun Alan Fung, Marianne van den Bree, Michael Owen, Kieran C Murphy, Maria Niarchou, Wendy R Kates,[...]. Am J Psychiatry 2014
386
15

An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities.
Erin B Kaminsky, Vineith Kaul, Justin Paschall, Deanna M Church, Brian Bunke, Dawn Kunig, Daniel Moreno-De-Luca, Andres Moreno-De-Luca, Jennifer G Mulle, Stephen T Warren,[...]. Genet Med 2011
286
15

The 3q29 microdeletion syndrome: report of three new unrelated patients and in silico "RNA binding" analysis of the 3q29 region.
Majed J Dasouki, Gerald H Lushington, Karine Hovanes, James Casey, Mereceds Gorre. Am J Med Genet A 2011
13
46

Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities.
Debra D'Angelo, Sébastien Lebon, Qixuan Chen, Sandra Martin-Brevet, LeeAnne Green Snyder, Loyse Hippolyte, Ellen Hanson, Anne M Maillard, W Andrew Faucett, Aurélien Macé,[...]. JAMA Psychiatry 2016
104
15

Copy number variation in bipolar disorder.
E K Green, E Rees, J T R Walters, K-G Smith, L Forty, D Grozeva, J L Moran, P Sklar, S Ripke, K D Chambert,[...]. Mol Psychiatry 2016
92
12

De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.
G Kirov, A J Pocklington, P Holmans, D Ivanov, M Ikeda, D Ruderfer, J Moran, K Chambert, D Toncheva, L Georgieva,[...]. Mol Psychiatry 2012
515
12

The 15q11.2 BP1-BP2 microdeletion syndrome: a review.
Devin M Cox, Merlin G Butler. Int J Mol Sci 2015
94
12

Further evidence for a male-selective genetic association of synapse-associated protein 97 (SAP97) gene with schizophrenia.
Akihito Uezato, Junko Kimura-Sato, Naoki Yamamoto, Yoshimi Iijima, Hiroshi Kunugi, Toru Nishikawa. Behav Brain Funct 2012
33
15

Copy number variation in schizophrenia in Sweden.
J P Szatkiewicz, C O'Dushlaine, G Chen, K Chambert, J L Moran, B M Neale, M Fromer, D Ruderfer, S Akterin, S E Bergen,[...]. Mol Psychiatry 2014
159
12

Phenotypic heterogeneity of genomic disorders and rare copy-number variants.
Santhosh Girirajan, Jill A Rosenfeld, Bradley P Coe, Sumit Parikh, Neil Friedman, Amy Goldstein, Robyn A Filipink, Juliann S McConnell, Brad Angle, Wendy S Meschino,[...]. N Engl J Med 2012
353
12

Synaptic, transcriptional and chromatin genes disrupted in autism.
Silvia De Rubeis, Xin He, Arthur P Goldberg, Christopher S Poultney, Kaitlin Samocha, A Erucment Cicek, Yan Kou, Li Liu, Menachem Fromer, Susan Walker,[...]. Nature 2014
12

Autism Spectrum Disorder, Developmental and Psychiatric Features in 16p11.2 Duplication.
LeeAnne Green Snyder, Debra D'Angelo, Qixuan Chen, Raphael Bernier, Robin P Goin-Kochel, Arianne Stevens Wallace, Jennifer Gerdts, Stephen Kanne, Leandra Berry, Lisa Blaskey,[...]. J Autism Dev Disord 2016
27
18

22q11.2 deletion syndrome.
Donna M McDonald-McGinn, Kathleen E Sullivan, Bruno Marino, Nicole Philip, Ann Swillen, Jacob A S Vorstman, Elaine H Zackai, Beverly S Emanuel, Joris R Vermeesch, Bernice E Morrow,[...]. Nat Rev Dis Primers 2015
381
12

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
12

16p11.2 deletion and duplication: Characterizing neurologic phenotypes in a large clinically ascertained cohort.
Kyle J Steinman, Sarah J Spence, Melissa B Ramocki, Monica B Proud, Sudha K Kessler, Elysa J Marco, LeeAnne Green Snyder, Debra D'Angelo, Qixuan Chen, Wendy K Chung,[...]. Am J Med Genet A 2016
70
12

The role of parental cognitive, behavioral, and motor profiles in clinical variability in individuals with chromosome 16p11.2 deletions.
Andres Moreno-De-Luca, David W Evans, K B Boomer, Ellen Hanson, Raphael Bernier, Robin P Goin-Kochel, Scott M Myers, Thomas D Challman, Daniel Moreno-De-Luca, Mylissa M Slane,[...]. JAMA Psychiatry 2015
86
12

Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder.
Ryan K C Yuen, Daniele Merico, Matt Bookman, Jennifer L Howe, Bhooma Thiruvahindrapuram, Rohan V Patel, Joe Whitney, Nicole Deflaux, Jonathan Bingham, Zhuozhi Wang,[...]. Nat Neurosci 2017
332
12

Behavioral changes and growth deficits in a CRISPR engineered mouse model of the schizophrenia-associated 3q29 deletion.
Timothy P Rutkowski, Ryan H Purcell, Rebecca M Pollak, Stephanie M Grewenow, Georgette M Gafford, Tamika Malone, Uswa A Khan, Jason P Schroeder, Michael P Epstein, Gary J Bassell,[...]. Mol Psychiatry 2021
12
41


De novo mutations in schizophrenia implicate synaptic networks.
Menachem Fromer, Andrew J Pocklington, David H Kavanagh, Hywel J Williams, Sarah Dwyer, Padhraig Gormley, Lyudmila Georgieva, Elliott Rees, Priit Palta, Douglas M Ruderfer,[...]. Nature 2014
955
10


16p13.11 duplication is a risk factor for a wide spectrum of neuropsychiatric disorders.
Arivudainambi Ramalingam, Xin-Gang Zhou, Stephanie D Fiedler, Sarah J Brawner, Julie M Joyce, Hong-Yu Liu, Shihui Yu. J Hum Genet 2011
70
10

Analysis of copy number variations at 15 schizophrenia-associated loci.
Elliott Rees, James T R Walters, Lyudmila Georgieva, Anthony R Isles, Kimberly D Chambert, Alexander L Richards, Gerwyn Mahoney-Davies, Sophie E Legge, Jennifer L Moran, Steven A McCarroll,[...]. Br J Psychiatry 2014
218
10


A polygenic burden of rare disruptive mutations in schizophrenia.
Shaun M Purcell, Jennifer L Moran, Menachem Fromer, Douglas Ruderfer, Nadia Solovieff, Panos Roussos, Colm O'Dushlaine, Kimberly Chambert, Sarah E Bergen, Anna Kähler,[...]. Nature 2014
875
10


1q21.1 Microduplication expression in adults.
Alessia Dolcetti, Candice K Silversides, Christian R Marshall, Anath C Lionel, Dimitri J Stavropoulos, Stephen W Scherer, Anne S Bassett. Genet Med 2013
58
10

Clinical phenotype of the recurrent 1q21.1 copy-number variant.
Raphael Bernier, Kyle J Steinman, Beau Reilly, Arianne Stevens Wallace, Elliott H Sherr, Nicholas Pojman, Heather C Mefford, Jennifer Gerdts, Rachel Earl, Ellen Hanson,[...]. Genet Med 2016
73
10

7q11.23 Duplication syndrome: Physical characteristics and natural history.
Colleen A Morris, Carolyn B Mervis, Alex P Paciorkowski, Omar Abdul-Rahman, Sarah L Dugan, Alan F Rope, Patricia Bader, Laura G Hendon, Shelley L Velleman, Bonita P Klein-Tasman,[...]. Am J Med Genet A 2015
37
10

Behavioral signatures related to genetic disorders in autism.
Hilgo Bruining, Marinus Jc Eijkemans, Martien Jh Kas, Sarah R Curran, Jacob As Vorstman, Patrick F Bolton. Mol Autism 2014
46
10


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.