A citation-based method for searching scientific literature

Ilaria Mannucci, Nghi D P Dang, Hannes Huber, Jaclyn B Murry, Jeff Abramson, Thorsten Althoff, Siddharth Banka, Gareth Baynam, David Bearden, Ana Beleza-Meireles, Paul J Benke, Siren Berland, Tatjana Bierhals, Frederic Bilan, Laurence A Bindoff, Geir Julius Braathen, Øyvind L Busk, Jirat Chenbhanich, Jonas Denecke, Luis F Escobar, Caroline Estes, Julie Fleischer, Daniel Groepper, Charlotte A Haaxma, Maja Hempel, Yolanda Holler-Managan, Gunnar Houge, Adam Jackson, Laura Kellogg, Boris Keren, Catherine Kiraly-Borri, Cornelia Kraus, Christian Kubisch, Gwenael Le Guyader, Ulf W Ljungblad, Leslie Manace Brenman, Julian A Martinez-Agosto, Matthew Might, David T Miller, Kelly Q Minks, Billur Moghaddam, Caroline Nava, Stanley F Nelson, John M Parant, Trine Prescott, Farrah Rajabi, Hanitra Randrianaivo, Simone F Reiter, Janneke Schuurs-Hoeijmakers, Perry B Shieh, Anne Slavotinek, Sarah Smithson, Alexander P A Stegmann, Kinga Tomczak, Kristian Tveten, Jun Wang, Jordan H Whitlock, Christiane Zweier, Kirsty McWalter, Jane Juusola, Fabiola Quintero-Rivera, Utz Fischer, Nan Cher Yeo, Hans-Jürgen Kreienkamp, Davor Lessel. Genome Med 2021
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


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
50

A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP.
Céline Helsmoortel, Anneke T Vulto-van Silfhout, Bradley P Coe, Geert Vandeweyer, Liesbeth Rooms, Jenneke van den Ende, Janneke H M Schuurs-Hoeijmakers, Carlo L Marcelis, Marjolein H Willemsen, Lisenka E L M Vissers,[...]. Nat Genet 2014
172
50

Epilepsy-associated genes.
Jie Wang, Zhi-Jian Lin, Liu Liu, Hai-Qing Xu, Yi-Wu Shi, Yong-Hong Yi, Na He, Wei-Ping Liao. Seizure 2017
117
50

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
50

Phosphoregulated FMRP phase separation models activity-dependent translation through bidirectional control of mRNA granule formation.
Brian Tsang, Jason Arsenault, Robert M Vernon, Hong Lin, Nahum Sonenberg, Lu-Yang Wang, Alaji Bah, Julie D Forman-Kay. Proc Natl Acad Sci U S A 2019
91
50

Recurrent de novo mutations in neurodevelopmental disorders: properties and clinical implications.
Amy B Wilfert, Arvis Sulovari, Tychele N Turner, Bradley P Coe, Evan E Eichler. Genome Med 2017
52
50

Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus.
Gea Beunders, Els Voorhoeve, Christelle Golzio, Luba M Pardo, Jill A Rosenfeld, Michael E Talkowski, Ingrid Simonic, Anath C Lionel, Sarah Vergult, Robert E Pyatt,[...]. Am J Hum Genet 2013
92
50

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism.
F Kyle Satterstrom, Jack A Kosmicki, Jiebiao Wang, Michael S Breen, Silvia De Rubeis, Joon-Yong An, Minshi Peng, Ryan Collins, Jakob Grove, Lambertus Klei,[...]. Cell 2020
310
50

Phenotypic spectrum and genotype-phenotype correlations of NRXN1 exon deletions.
Christian P Schaaf, Philip M Boone, Srirangan Sampath, Charles Williams, Patricia I Bader, Jennifer M Mueller, Oleg A Shchelochkov, Chester W Brown, Heather P Crawford, James A Phalen,[...]. Eur J Hum Genet 2012
70
50

Comprehensive genetic analysis of 57 families with clinically suspected Cornelia de Lange syndrome.
Hiromi Aoi, Takeshi Mizuguchi, José Ricard Ceroni, Veronica Eun Hue Kim, Isabel Furquim, Rachel S Honjo, Takuma Iwaki, Toshifumi Suzuki, Futoshi Sekiguchi, Yuri Uchiyama,[...]. J Hum Genet 2019
17
50

De Novo Missense Mutations in DHX30 Impair Global Translation and Cause a Neurodevelopmental Disorder.
Davor Lessel, Claudia Schob, Sébastien Küry, Margot R F Reijnders, Tamar Harel, Mohammad K Eldomery, Zeynep Coban-Akdemir, Jonas Denecke, Shimon Edvardson, Estelle Colin,[...]. Am J Hum Genet 2017
30
50

A report of gonadal mosaicism in DHX30-related neurodevelopmental disorder.
Laura A Cross, Kirsty McWalter, Jennifer Keller-Ramey, Lindsay B Henderson, Shivarajan M Amudhavalli. Clin Dysmorphol 2020
5
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.