A citation-based method for searching scientific literature

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, Stephen T Warren, David Weinshenker, Tamara Caspary, Jennifer Gladys Mulle. Mol Psychiatry 2021
Times Cited: 12







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



Times Cited
  Times     Co-cited
Similarity


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
41


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
33



PAK2 Haploinsufficiency Results in Synaptic Cytoskeleton Impairment and Autism-Related Behavior.
Yan Wang, Cheng Zeng, Jinchen Li, Zikai Zhou, Xingda Ju, Shuting Xia, Yuanyuan Li, An Liu, Huajing Teng, Kun Zhang,[...]. Cell Rep 2018
24
33

Psychiatric-disorder-related behavioral phenotypes and cortical hyperactivity in a mouse model of 3q29 deletion syndrome.
Masayuki Baba, Kazumasa Yokoyama, Kaoru Seiriki, Yuichiro Naka, Kensuke Matsumura, Momoka Kondo, Kana Yamamoto, Misuzu Hayashida, Atsushi Kasai, Yukio Ago,[...]. Neuropsychopharmacology 2019
11
36


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
40

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


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
25

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
25

Pervasive genetic interactions modulate neurodevelopmental defects of the autism-associated 16p11.2 deletion in Drosophila melanogaster.
Janani Iyer, Mayanglambam Dhruba Singh, Matthew Jensen, Payal Patel, Lucilla Pizzo, Emily Huber, Haley Koerselman, Alexis T Weiner, Paola Lepanto, Komal Vadodaria,[...]. Nat Commun 2018
19
25

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
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

Binding properties and dynamic localization of an alternative isoform of the cap-binding complex subunit CBP20.
Marta Pabis, Noa Neufeld, Yaron Shav-Tal, Karla M Neugebauer. Nucleus 2010
13
25

A systematic analysis of human disease-associated gene sequences in Drosophila melanogaster.
L T Reiter, L Potocki, S Chien, M Gribskov, E Bier. Genome Res 2001
462
25

Human copy number variation and complex genetic disease.
Santhosh Girirajan, Catarina D Campbell, Evan E Eichler. Annu Rev Genet 2011
207
25

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
25

A copy number variation morbidity map of developmental delay.
Gregory M Cooper, Bradley P Coe, Santhosh Girirajan, Jill A Rosenfeld, Tiffany H Vu, Carl Baker, Charles Williams, Heather Stalker, Rizwan Hamid, Vickie Hannig,[...]. Nat Genet 2011
803
25

Kctd13 deletion reduces synaptic transmission via increased RhoA.
Christine Ochoa Escamilla, Irina Filonova, Angela K Walker, Zhong X Xuan, Roopashri Holehonnur, Felipe Espinosa, Shunan Liu, Summer B Thyme, Isabel A López-García, Dorian B Mendoza,[...]. Nature 2017
49
25

Behavioral abnormalities and circuit defects in the basal ganglia of a mouse model of 16p11.2 deletion syndrome.
Thomas Portmann, Mu Yang, Rong Mao, Georgia Panagiotakos, Jacob Ellegood, Gul Dolen, Patrick L Bader, Brad A Grueter, Carleton Goold, Elaine Fisher,[...]. Cell Rep 2014
114
25

A mouse model of the schizophrenia-associated 1q21.1 microdeletion syndrome exhibits altered mesolimbic dopamine transmission.
Jacob Nielsen, Kim Fejgin, Florence Sotty, Vibeke Nielsen, Arne Mørk, Claus T Christoffersen, Leonid Yavich, Jes B Lauridsen, Dorte Clausen, Peter H Larsen,[...]. Transl Psychiatry 2017
21
25

KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant.
Christelle Golzio, Jason Willer, Michael E Talkowski, Edwin C Oh, Yu Taniguchi, Sébastien Jacquemont, Alexandre Reymond, Mei Sun, Akira Sawa, James F Gusella,[...]. Nature 2012
235
25

Fbxo45 forms a novel ubiquitin ligase complex and is required for neuronal development.
Toru Saiga, Takaichi Fukuda, Masaki Matsumoto, Hirobumi Tada, Hirotaka James Okano, Hideyuki Okano, Keiichi I Nakayama. Mol Cell Biol 2009
78
16

Unraveling the genetic architecture of copy number variants associated with schizophrenia and other neuropsychiatric disorders.
Timothy P Rutkowski, Jason P Schroeder, Georgette M Gafford, Stephen T Warren, David Weinshenker, Tamara Caspary, Jennifer G Mulle. J Neurosci Res 2017
21
16

Sept5 deficiency exerts pleiotropic influence on affective behaviors and cognitive functions in mice.
Go Suzuki, Kathryn M Harper, Takeshi Hiramoto, Takehito Sawamura, MoonSook Lee, Gina Kang, Kenji Tanigaki, Mahalah Buell, Mark A Geyer, William S Trimble,[...]. Hum Mol Genet 2009
52
16


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
16


edgeR: a Bioconductor package for differential expression analysis of digital gene expression data.
Mark D Robinson, Davis J McCarthy, Gordon K Smyth. Bioinformatics 2010
16

Human intellectual disability genes form conserved functional modules in Drosophila.
Merel A W Oortveld, Shivakumar Keerthikumar, Martin Oti, Bonnie Nijhof, Ana Clara Fernandes, Korinna Kochinke, Anna Castells-Nobau, Eva van Engelen, Thijs Ellenkamp, Lilian Eshuis,[...]. PLoS Genet 2013
29
16

22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia.
Maria Karayiorgou, Tony J Simon, Joseph A Gogos. Nat Rev Neurosci 2010
297
16


A Drosophila model for Angelman syndrome.
Yaning Wu, Francois V Bolduc, Kimberly Bell, Tim Tully, Yanshan Fang, Amita Sehgal, Janice A Fischer. Proc Natl Acad Sci U S A 2008
68
16

Genetic modifiers of MeCP2 function in Drosophila.
Holly N Cukier, Alma M Perez, Ann L Collins, Zhaolan Zhou, Huda Y Zoghbi, Juan Botas. PLoS Genet 2008
45
16

Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice.
E A Lindsay, F Vitelli, H Su, M Morishima, T Huynh, T Pramparo, V Jurecic, G Ogunrinu, H F Sutherland, P J Scambler,[...]. Nature 2001
677
16


Mouse Genome Database (MGD) 2019.
Carol J Bult, Judith A Blake, Cynthia L Smith, James A Kadin, Joel E Richardson. Nucleic Acids Res 2019
202
16

Transcriptional and behavioral interaction between 22q11.2 orthologs modulates schizophrenia-related phenotypes in mice.
Marta Paterlini, Stanislav S Zakharenko, Wen-Sung Lai, Jie Qin, Hui Zhang, Jun Mukai, Koen G C Westphal, Berend Olivier, David Sulzer, Paul Pavlidis,[...]. Nat Neurosci 2005
181
16

Fruit flies in biomedical research.
Michael F Wangler, Shinya Yamamoto, Hugo J Bellen. Genetics 2015
87
16

Understanding multicellular function and disease with human tissue-specific networks.
Casey S Greene, Arjun Krishnan, Aaron K Wong, Emanuela Ricciotti, Rene A Zelaya, Daniel S Himmelstein, Ran Zhang, Boris M Hartmann, Elena Zaslavsky, Stuart C Sealfon,[...]. Nat Genet 2015
362
16

Using FlyAtlas to identify better Drosophila melanogaster models of human disease.
Venkateswara R Chintapalli, Jing Wang, Julian A T Dow. Nat Genet 2007
16

HTSeq--a Python framework to work with high-throughput sequencing data.
Simon Anders, Paul Theodor Pyl, Wolfgang Huber. Bioinformatics 2015
16


Quantitative Assessment of Eye Phenotypes for Functional Genetic Studies Using Drosophila melanogaster.
Janani Iyer, Qingyu Wang, Thanh Le, Lucilla Pizzo, Sebastian Grönke, Surendra S Ambegaokar, Yuzuru Imai, Ashutosh Srivastava, Beatriz Llamusí Troisí, Graeme Mardon,[...]. G3 (Bethesda) 2016
22
16

An integrative approach to ortholog prediction for disease-focused and other functional studies.
Yanhui Hu, Ian Flockhart, Arunachalam Vinayagam, Clemens Bergwitz, Bonnie Berger, Norbert Perrimon, Stephanie E Mohr. BMC Bioinformatics 2011
280
16

Building an ommatidium one cell at a time.
Justin P Kumar. Dev Dyn 2012
71
16


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.