A citation-based method for searching scientific literature

Rossana Sanchez Russo, Michael J Gambello, Melissa M Murphy, Katrina Aberizk, Emily Black, T Lindsey Burrell, Grace Carlock, Joseph F Cubells, Michael T Epstein, Roberto Espana, Katrina Goines, Ryan M Guest, Cheryl Klaiman, Sookyong Koh, Elizabeth J Leslie, Longchuan Li, Derek M Novacek, Celine A Saulnier, Esra Sefik, Sarah Shultz, Elaine Walker, Stormi Pulver White, Jennifer Gladys Mulle. Genet Med 2021
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


NCBP2 modulates neurodevelopmental defects of the 3q29 deletion in Drosophila and Xenopus laevis models.
Mayanglambam Dhruba Singh, Matthew Jensen, Micaela Lasser, Emily Huber, Tanzeen Yusuff, Lucilla Pizzo, Brian Lifschutz, Inshya Desai, Alexis Kubina, Sneha Yennawar,[...]. PLoS Genet 2020
8
50



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
50

Novel features of 3q29 deletion syndrome: Results from the 3q29 registry.
Megan R Glassford, Jill A Rosenfeld, Alexa A Freedman, Michael E Zwick, Jennifer G Mulle. Am J Med Genet A 2016
39
50

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
159
50

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
614
50

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
50


Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern.
E M Moss, M L Batshaw, C B Solot, M Gerdes, D M McDonald-McGinn, D A Driscoll, B S Emanuel, E H Zackai, P P Wang. J Pediatr 1999
217
50

Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome.
Robert W Davies, Ania M Fiksinski, Elemi J Breetvelt, Nigel M Williams, Stephen R Hooper, Thomas Monfeuga, Anne S Bassett, Michael J Owen, Raquel E Gur, Bernice E Morrow,[...]. Nat Med 2020
20
50

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
405
50

Identification of Neuropsychiatric Copy Number Variants in a Health Care System Population.
Christa Lese Martin, Karen E Wain, Matthew T Oetjens, Kasia Tolwinski, Emily Palen, Abby Hare-Harris, Lukas Habegger, Evan K Maxwell, Jeffrey G Reid, Lauren Kasparson Walsh,[...]. JAMA Psychiatry 2020
13
50

A framework for the investigation of rare genetic disorders in neuropsychiatry.
Stephan J Sanders, Mustafa Sahin, Joseph Hostyk, Audrey Thurm, Sebastien Jacquemont, Paul Avillach, Elise Douard, Christa L Martin, Meera E Modi, Andres Moreno-De-Luca,[...]. Nat Med 2019
30
50

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
50

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
25

Comprehensive phenotyping of neuropsychiatric traits in a multiplex 3q29 deletion family: a case report.
Melissa M Murphy, T Lindsey Burrell, Joseph F Cubells, Michael T Epstein, Roberto Espana, Michael J Gambello, Katrina Goines, Cheryl Klaiman, Sookyong Koh, Rossana Sanchez Russo,[...]. BMC Psychiatry 2020
3
33


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
25

Optimizing Genetic Diagnosis of Neurodevelopmental Disorders in the Clinical Setting.
David Joshua Michelson, Robin Dawn Clark. Clin Lab Med 2020
2
50

Craniofacial features of 3q29 deletion syndrome: Application of next-generation phenotyping technology.
Bryan C Mak, Rossana Sanchez Russo, Michael J Gambello, Nicole Fleischer, Emily D Black, Elizabeth Leslie, Melissa M Murphy, Jennifer Gladys Mulle. Am J Med Genet A 2021
1
100

Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources.
Sebastian Köhler, Leigh Carmody, Nicole Vasilevsky, Julius O B Jacobsen, Daniel Danis, Jean-Philippe Gourdine, Michael Gargano, Nomi L Harris, Nicolas Matentzoglu, Julie A McMurry,[...]. Nucleic Acids Res 2019
231
25

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
25

Identifying facial phenotypes of genetic disorders using deep learning.
Yaron Gurovich, Yair Hanani, Omri Bar, Guy Nadav, Nicole Fleischer, Dekel Gelbman, Lina Basel-Salmon, Peter M Krawitz, Susanne B Kamphausen, Martin Zenker,[...]. Nat Med 2019
132
25

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
375
25

Evaluating Face2Gene as a Tool to Identify Cornelia de Lange Syndrome by Facial Phenotypes.
Ana Latorre-Pellicer, Ángela Ascaso, Laura Trujillano, Marta Gil-Salvador, Maria Arnedo, Cristina Lucia-Campos, Rebeca Antoñanzas-Pérez, Iñigo Marcos-Alcalde, Ilaria Parenti, Gloria Bueno-Lozano,[...]. Int J Mol Sci 2020
7
25

Shared facial phenotype of patients with mucolipidosis type IV: A clinical observation reaffirmed by next generation phenotyping.
Ben Pode-Shakked, Yael Finezilber, Yonit Levi, Shiri Liber, Nicole Fleischer, Lior Greenbaum, Annick Raas-Rothschild. Eur J Med Genet 2020
4
25

Cognitive profile in a large French cohort of adults with Prader-Willi syndrome: differences between genotypes.
P Copet, J Jauregi, V Laurier, V Ehlinger, C Arnaud, A-M Cobo, C Molinas, M Tauber, D Thuilleaux. J Intellect Disabil Res 2010
41
25

Morphological differences in the mirror neuron system in Williams syndrome.
Rowena Ng, Timothy T Brown, Matthew Erhart, Anna M Järvinen, Julie R Korenberg, Ursula Bellugi, Eric Halgren. Soc Neurosci 2016
4
25

Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.
Stephan J Sanders, A Gulhan Ercan-Sencicek, Vanessa Hus, Rui Luo, Michael T Murtha, Daniel Moreno-De-Luca, Su H Chu, Michael P Moreau, Abha R Gupta, Susanne A Thomson,[...]. Neuron 2011
806
25

Deviant trajectories of cortical maturation in 22q11.2 deletion syndrome (22q11DS): a cross-sectional and longitudinal study.
Marie Schaer, Martin Debbané, Meritxell Bach Cuadra, Marie-Christine Ottet, Bronwyn Glaser, Jean-Philippe Thiran, Stephan Eliez. Schizophr Res 2009
85
25


Performance on the Kaufman Brief Intelligence Test-2 by Children With Williams Syndrome.
C Holley Pitts, Carolyn B Mervis. Am J Intellect Dev Disabil 2016
8
25

Deficits in voice and multisensory processing in patients with Prader-Willi syndrome.
Juliette Salles, Kuzma Strelnikov, Mantoulan Carine, Thuilleaux Denise, Virginie Laurier, Catherine Molinas, Maïthé Tauber, Pascal Barone. Neuropsychologia 2016
7
25

Effects of a functional COMT polymorphism on brain anatomy and cognitive function in adults with velo-cardio-facial syndrome.
T van Amelsvoort, J Zinkstok, M Figee, E Daly, R Morris, M J Owen, K C Murphy, L De Haan, D H Linszen, B Glaser,[...]. Psychol Med 2008
38
25


Abnormalities in gray matter microstructure in young adults with 22q11.2 deletion syndrome.
Zora Kikinis, Nikos Makris, Valerie J Sydnor, Sylvain Bouix, Ofer Pasternak, Ioana L Coman, Kevin M Antshel, Wanda Fremont, Marek R Kubicki, Martha E Shenton,[...]. Neuroimage Clin 2019
4
25

The relationship between compulsive behaviour and academic achievement across the three genetic subtypes of Prader-Willi syndrome.
J Zarcone, D Napolitano, C Peterson, J Breidbord, S Ferraioli, M Caruso-Anderson, L Holsen, M G Butler, T Thompson. J Intellect Disabil Res 2007
40
25

Genotype-phenotype associations in children with copy number variants associated with high neuropsychiatric risk in the UK (IMAGINE-ID): a case-control cohort study.
Samuel J R A Chawner, Michael J Owen, Peter Holmans, F Lucy Raymond, David Skuse, Jeremy Hall, Marianne B M van den Bree. Lancet Psychiatry 2019
34
25

Facial emotion processing in patients with social anxiety disorder and Williams-Beuren syndrome: an fMRI study.
Cynthia Binelli, Armando Muñiz, Susana Subira, Ricard Navines, Laura Blanco-Hinojo, Debora Perez-Garcia, Jose Crippa, Magi Farré, Luis Pérez-Jurado, Jesus Pujol,[...]. J Psychiatry Neurosci 2016
10
25

Neuropsychological profile of children and adolescents with the 22q11.2 microdeletion.
M Woodin, P P Wang, D Aleman, D McDonald-McGinn, E Zackai, E Moss. Genet Med 2001
175
25

Language characterization in 16p11.2 deletion and duplication syndromes.
So Hyun Kim, LeeAnne Green-Snyder, Catherine Lord, Somer Bishop, Kyle J Steinman, Raphael Bernier, Ellen Hanson, Robin P Goin-Kochel, Wendy K Chung. Am J Med Genet B Neuropsychiatr Genet 2020
4
25

Clinical implications of copy number variations in autoimmune disorders.
Seon-Hee Yim, Seung-Hyun Jung, Boram Chung, Yeun-Jun Chung. Korean J Intern Med 2015
8
25

Relative burden of large CNVs on a range of neurodevelopmental phenotypes.
Santhosh Girirajan, Zoran Brkanac, Bradley P Coe, Carl Baker, Laura Vives, Tiffany H Vu, Neil Shafer, Raphael Bernier, Giovanni B Ferrero, Margherita Silengo,[...]. PLoS Genet 2011
206
25

Cognitive functioning in adults with Williams syndrome.
P Howlin, M Davies, O Udwin. J Child Psychol Psychiatry 1998
98
25

Tetralogy of Fallot associated with chromosome 22q11.2 deletion in adolescents and young adults.
K Momma, A Takao, R Matsuoka, Y Imai, A Muto, M Osawa, M Takayama. Genet Med 2001
18
25

Cognitive abilities and genotype in a population-based sample of people with Prader-Willi syndrome.
J Whittington, A Holland, T Webb, J Butler, D Clarke, H Boer. J Intellect Disabil Res 2004
107
25

3D pattern of brain abnormalities in Williams syndrome visualized using tensor-based morphometry.
Ming-Chang Chiang, Allan L Reiss, Agatha D Lee, Ursula Bellugi, Albert M Galaburda, Julie R Korenberg, Debra L Mills, Arthur W Toga, Paul M Thompson. Neuroimage 2007
107
25

Cognitive Performance Among Carriers of Pathogenic Copy Number Variants: Analysis of 152,000 UK Biobank Subjects.
Kimberley M Kendall, Elliott Rees, Valentina Escott-Price, Mark Einon, Rhys Thomas, Jonathan Hewitt, Michael C O'Donovan, Michael J Owen, James T R Walters, George Kirov. Biol Psychiatry 2017
74
25

Copy Number Variation Disorders.
Tamim H Shaikh. Curr Genet Med Rep 2017
10
25


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.