A citation-based method for searching scientific literature

Tanzeen Yusuff, Matthew Jensen, Sneha Yennawar, Lucilla Pizzo, Siddharth Karthikeyan, Dagny J Gould, Avik Sarker, Erika Gedvilaite, Yurika Matsui, Janani Iyer, Zhi-Chun Lai, Santhosh Girirajan. PLoS Genet 2020
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


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
16
100

Human copy number variation and complex genetic disease.
Santhosh Girirajan, Catarina D Campbell, Evan E Eichler. Annu Rev Genet 2011
207
100

Over-expression of DSCAM and COL6A2 cooperatively generates congenital heart defects.
Tamar R Grossman, Amir Gamliel, Robert J Wessells, Ouarda Taghli-Lamallem, Kristen Jepsen, Karen Ocorr, Julie R Korenberg, Kirk L Peterson, Michael G Rosenfeld, Rolf Bodmer,[...]. PLoS Genet 2011
46
100

Association between microdeletion and microduplication at 16p11.2 and autism.
Lauren A Weiss, Yiping Shen, Joshua M Korn, Dan E Arking, David T Miller, Ragnheidur Fossdal, Evald Saemundsen, Hreinn Stefansson, Manuel A R Ferreira, Todd Green,[...]. N Engl J Med 2008
100

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
7
100

Genome-wide prediction and functional characterization of the genetic basis of autism spectrum disorder.
Arjun Krishnan, Ran Zhang, Victoria Yao, Chandra L Theesfeld, Aaron K Wong, Alicja Tadych, Natalia Volfovsky, Alan Packer, Alex Lash, Olga G Troyanskaya. Nat Neurosci 2016
136
100

The 16p11.2 homologs fam57ba and doc2a generate certain brain and body phenotypes.
Jasmine M McCammon, Alicia Blaker-Lee, Xiao Chen, Hazel Sive. Hum Mol Genet 2017
12
100

Oligogenic Effects of 16p11.2 Copy-Number Variation on Craniofacial Development.
Yuqi Qiu, Thomas Arbogast, Sandra Martin Lorenzo, Hongying Li, Shih C Tang, Ellen Richardson, Oanh Hong, Shawn Cho, Omar Shanta, Timothy Pang,[...]. Cell Rep 2019
11
100

Mutations in RAI1 associated with Smith-Magenis syndrome.
Rebecca E Slager, Tiffany Lynn Newton, Christopher N Vlangos, Brenda Finucane, Sarah H Elsea. Nat Genet 2003
199
50

Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies.
Heather C Mefford, Hiltrud Muhle, Philipp Ostertag, Sarah von Spiczak, Karen Buysse, Carl Baker, Andre Franke, Alain Malafosse, Pierre Genton, Pierre Thomas,[...]. PLoS Genet 2010
326
50

Population prevalence and inheritance pattern of recurrent CNVs associated with neurodevelopmental disorders in 12,252 newborns and their parents.
Dinka Smajlagić, Ksenia Lavrichenko, Siren Berland, Øyvind Helgeland, Gun Peggy Knudsen, Marc Vaudel, Jan Haavik, Per Morten Knappskog, Pål Rasmus Njølstad, Gunnar Houge,[...]. Eur J Hum Genet 2021
3
50

The zebrafish reference genome sequence and its relationship to the human genome.
Kerstin Howe, Matthew D Clark, Carlos F Torroja, James Torrance, Camille Berthelot, Matthieu Muffato, John E Collins, Sean Humphray, Karen McLaren, Lucy Matthews,[...]. Nature 2013
50

Mutations in NCAPG2 Cause a Severe Neurodevelopmental Syndrome that Expands the Phenotypic Spectrum of Condensinopathies.
Tahir N Khan, Kamal Khan, Azita Sadeghpour, Hannah Reynolds, Yezmin Perilla, Marie T McDonald, William B Gallentine, Shahid M Baig, Erica E Davis, Nicholas Katsanis. Am J Hum Genet 2019
8
50

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
50

Speech delays and behavioral problems are the predominant features in individuals with developmental delays and 16p11.2 microdeletions and microduplications.
Jill A Rosenfeld, Justine Coppinger, Bassem A Bejjani, Santhosh Girirajan, Evan E Eichler, Lisa G Shaffer, Blake C Ballif. J Neurodev Disord 2010
104
50

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
44
50

Circadian Rhythms and Sleep in Drosophila melanogaster.
Christine Dubowy, Amita Sehgal. Genetics 2017
123
50

Otud7a Knockout Mice Recapitulate Many Neurological Features of 15q13.3 Microdeletion Syndrome.
Jiani Yin, Wu Chen, Eugene S Chao, Sirena Soriano, Li Wang, Wei Wang, Steven E Cummock, Huifang Tao, Kaifang Pang, Zhandong Liu,[...]. Am J Hum Genet 2018
26
50

Genetic Drivers of Kidney Defects in the DiGeorge Syndrome.
Esther Lopez-Rivera, Yangfan P Liu, Miguel Verbitsky, Blair R Anderson, Valentina P Capone, Edgar A Otto, Zhonghai Yan, Adele Mitrotti, Jeremiah Martino, Nicholas J Steers,[...]. N Engl J Med 2017
61
50

Dosage changes of a segment at 17p13.1 lead to intellectual disability and microcephaly as a result of complex genetic interaction of multiple genes.
Claudia M B Carvalho, Shivakumar Vasanth, Marwan Shinawi, Chad Russell, Melissa B Ramocki, Chester W Brown, Jesper Graakjaer, Anne-Bine Skytte, Angela M Vianna-Morgante, Ana C V Krepischi,[...]. Am J Hum Genet 2014
28
50


Altered TAOK2 activity causes autism-related neurodevelopmental and cognitive abnormalities through RhoA signaling.
Melanie Richter, Nadeem Murtaza, Robin Scharrenberg, Sean H White, Ole Johanns, Susan Walker, Ryan K C Yuen, Birgit Schwanke, Bianca Bedürftig, Melad Henis,[...]. Mol Psychiatry 2019
40
50

The Immune Signaling Adaptor LAT Contributes to the Neuroanatomical Phenotype of 16p11.2 BP2-BP3 CNVs.
Maria Nicla Loviglio, Thomas Arbogast, Aia Elise Jønch, Stephan C Collins, Konstantin Popadin, Camille S Bonnet, Giuliana Giannuzzi, Anne M Maillard, Sébastien Jacquemont, Binnaz Yalcin,[...]. Am J Hum Genet 2017
15
50

De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot.
Steven C Greenway, Alexandre C Pereira, Jennifer C Lin, Steven R DePalma, Samuel J Israel, Sonia M Mesquita, Emel Ergul, Jessie H Conta, Joshua M Korn, Steven A McCarroll,[...]. Nat Genet 2009
293
50

RAS-MAPK-MSK1 pathway modulates ataxin 1 protein levels and toxicity in SCA1.
Jeehye Park, Ismael Al-Ramahi, Qiumin Tan, Nissa Mollema, Javier R Diaz-Garcia, Tatiana Gallego-Flores, Hsiang-Chih Lu, Sarita Lagalwar, Lisa Duvick, Hyojin Kang,[...]. Nature 2013
87
50

Genomic changes detected by array CGH in human embryos with developmental defects.
E Rajcan-Separovic, Y Qiao, C Tyson, C Harvard, C Fawcett, D Kalousek, M Stephenson, T Philipp. Mol Hum Reprod 2010
32
50


Fetal phenotype associated with the 22q11 deletion.
Anne-Claire Noël, Fanny Pelluard, Anne-Lise Delezoide, Louise Devisme, Laurence Loeuillet, Brigitte Leroy, Alain Martin, Raymonde Bouvier, Annie Laquerriere, Corinne Jeanne-Pasquier,[...]. Am J Med Genet A 2014
24
50

Chrna7 deficient mice manifest no consistent neuropsychiatric and behavioral phenotypes.
Jiani Yin, Wu Chen, Hongxing Yang, Mingshan Xue, Christian P Schaaf. Sci Rep 2017
21
50

A common molecular mechanism underlies two phenotypically distinct 17p13.1 microdeletion syndromes.
Adam Shlien, Berivan Baskin, Maria Isabel W Achatz, Dimitrios J Stavropoulos, Kim E Nichols, Louanne Hudgins, Chantal F Morel, Margaret P Adam, Nataliya Zhukova, Lianne Rotin,[...]. Am J Hum Genet 2010
25
50

A new highly penetrant form of obesity due to deletions on chromosome 16p11.2.
R G Walters, S Jacquemont, A Valsesia, A J de Smith, D Martinet, J Andersson, M Falchi, F Chen, J Andrieux, S Lobbens,[...]. Nature 2010
315
50

Dendritic spine pathology in neuropsychiatric disorders.
Peter Penzes, Michael E Cahill, Kelly A Jones, Jon-Eric VanLeeuwen, Kevin M Woolfrey. Nat Neurosci 2011
856
50

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
23
50

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
231
50

Molecular and Neural Functions of Rai1, the Causal Gene for Smith-Magenis Syndrome.
Wei-Hsiang Huang, Casey J Guenthner, Jin Xu, Tiffany Nguyen, Lindsay A Schwarz, Alex W Wilkinson, Or Gozani, Howard Y Chang, Mehrdad Shamloo, Liqun Luo. Neuron 2016
24
50

Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes.
M N Loviglio, M Leleu, K Männik, M Passeggeri, G Giannuzzi, I van der Werf, S M Waszak, M Zazhytska, I Roberts-Caldeira, N Gheldof,[...]. Mol Psychiatry 2017
34
50


Genotype-phenotype correlation in Smith-Magenis syndrome: evidence that multiple genes in 17p11.2 contribute to the clinical spectrum.
Santhosh Girirajan, Christopher N Vlangos, Barbara B Szomju, Emily Edelman, Christopher D Trevors, Lucie Dupuis, Marjan Nezarati, David J Bunyan, Sarah H Elsea. Genet Med 2006
82
50

Recurrent 16p11.2 microdeletions in autism.
Ravinesh A Kumar, Samer KaraMohamed, Jyotsna Sudi, Donald F Conrad, Camille Brune, Judith A Badner, T Conrad Gilliam, Norma J Nowak, Edwin H Cook, William B Dobyns,[...]. Hum Mol Genet 2008
458
50


Habituation Learning Is a Widely Affected Mechanism in Drosophila Models of Intellectual Disability and Autism Spectrum Disorders.
Michaela Fenckova, Laura E R Blok, Lenke Asztalos, David P Goodman, Pavel Cizek, Euginia L Singgih, Jeffrey C Glennon, Joanna IntHout, Christiane Zweier, Evan E Eichler,[...]. Biol Psychiatry 2019
13
50


Mutations of RAI1, a PHD-containing protein, in nondeletion patients with Smith-Magenis syndrome.
Weimin Bi, G Mustafa Saifi, Christine J Shaw, Katherina Walz, Patricia Fonseca, Meredith Wilson, Lorraine Potocki, James R Lupski. Hum Genet 2004
77
50

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
455
50

Copy number variation in human health, disease, and evolution.
Feng Zhang, Wenli Gu, Matthew E Hurles, James R Lupski. Annu Rev Genomics Hum Genet 2009
683
50

CRISPR/Cas9-mediated Knockout of the Neuropsychiatric Risk Gene KCTD13 Causes Developmental Deficits in Human Cortical Neurons Derived from Induced Pluripotent Stem Cells.
Valeria Kizner, Maximilian Naujock, Sandra Fischer, Stefan Jäger, Selina Reich, Ines Schlotthauer, Kai Zuckschwerdt, Tobias Geiger, Tobias Hildebrandt, Nathan Lawless,[...]. Mol Neurobiol 2020
6
50

Systems Analysis of the 22q11.2 Microdeletion Syndrome Converges on a Mitochondrial Interactome Necessary for Synapse Function and Behavior.
Avanti Gokhale, Cortnie Hartwig, Amanda A H Freeman, Julia L Bassell, Stephanie A Zlatic, Christie Sapp Savas, Trishna Vadlamudi, Farida Abudulai, Tyler T Pham, Amanda Crocker,[...]. J Neurosci 2019
16
50

AMPK signaling linked to the schizophrenia-associated 1q21.1 deletion is required for neuronal and sleep maintenance.
Stanislav Nagy, Gianna W Maurer, Julie L Hentze, Morten Rose, Thomas M Werge, Kim Rewitz. PLoS Genet 2018
5
50


In vivo modeling of the morbid human genome using Danio rerio.
Adrienne R Niederriter, Erica E Davis, Christelle Golzio, Edwin C Oh, I-Chun Tsai, Nicholas Katsanis. J Vis Exp 2013
42
50


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.