A citation-based method for searching scientific literature

David B Beck, Mohammed A Basar, Anthony J Asmar, Joyce J Thompson, Hirotsugu Oda, Daniela T Uehara, Ken Saida, Sander Pajusalu, Inga Talvik, Precilla D'Souza, Joann Bodurtha, Weiyi Mu, Kristin W Barañano, Noriko Miyake, Raymond Wang, Marlies Kempers, Tomoko Tamada, Yutaka Nishimura, Satoshi Okada, Tomoki Kosho, Ryan Dale, Apratim Mitra, Ellen Macnamara, Naomichi Matsumoto, Johji Inazawa, Magdalena Walkiewicz, Katrin Õunap, Cynthia J Tifft, Ivona Aksentijevich, Daniel L Kastner, Pedro P Rocha, Achim Werner. Sci Adv 2021
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


Deubiquitylases in developmental ubiquitin signaling and congenital diseases.
Mohammed A Basar, David B Beck, Achim Werner. Cell Death Differ 2021
21
66

X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes.
H Hu, S A Haas, J Chelly, H Van Esch, M Raynaud, A P M de Brouwer, S Weinert, G Froyen, S G M Frints, F Laumonnier,[...]. Mol Psychiatry 2016
170
66

An X-linked syndrome with severe neurodevelopmental delay, hydrocephalus, and early lethality caused by a missense variation in the OTUD5 gene.
Kornelia Tripolszki, Erina Sasaki, Ronja Hotakainen, Abdul Halim Kassim, Catarina Pereira, Arndt Rolfs, Peter Bauer, William Reardon, Aida M Bertoli-Avella. Clin Genet 2021
4
75

Syndromic X-linked intellectual disability segregating with a missense variant in RLIM.
Elin Tønne, Rita Holdhus, Christine Stansberg, Asbjørg Stray-Pedersen, Kjell Petersen, Han G Brunner, Christian Gilissen, Alexander Hoischen, Trine Prescott, Vidar M Steen,[...]. Eur J Hum Genet 2015
18
50

Biallelic Variants in OTUD6B Cause an Intellectual Disability Syndrome Associated with Seizures and Dysmorphic Features.
Teresa Santiago-Sim, Lindsay C Burrage, Frédéric Ebstein, Mari J Tokita, Marcus Miller, Weimin Bi, Alicia A Braxton, Jill A Rosenfeld, Maher Shahrour, Andrea Lehmann,[...]. Am J Hum Genet 2017
36
50

REX1 is the critical target of RNF12 in imprinted X chromosome inactivation in mice.
Cristina Gontan, Hegias Mira-Bontenbal, Aristea Magaraki, Catherine Dupont, Tahsin Stefan Barakat, Eveline Rentmeester, Jeroen Demmers, Joost Gribnau. Nat Commun 2018
15
50

X-linked intellectual disability update 2017.
Giovanni Neri, Charles E Schwartz, Herbert A Lubs, Roger E Stevenson. Am J Med Genet A 2018
59
33

Phosphorylation-dependent activity of the deubiquitinase DUBA.
Oscar W Huang, Xiaolei Ma, JianPing Yin, Jeremy Flinders, Till Maurer, Nobuhiko Kayagaki, Qui Phung, Ivan Bosanac, David Arnott, Vishva M Dixit,[...]. Nat Struct Mol Biol 2012
76
33

Breaking the chains: structure and function of the deubiquitinases.
David Komander, Michael J Clague, Sylvie Urbé. Nat Rev Mol Cell Biol 2009
33

OTU deubiquitinases reveal mechanisms of linkage specificity and enable ubiquitin chain restriction analysis.
Tycho E T Mevissen, Manuela K Hospenthal, Paul P Geurink, Paul R Elliott, Masato Akutsu, Nadia Arnaudo, Reggy Ekkebus, Yogesh Kulathu, Tobias Wauer, Farid El Oualid,[...]. Cell 2013
340
33

UBR7 functions with UBR5 in the Notch signaling pathway and is involved in a neurodevelopmental syndrome with epilepsy, ptosis, and hypothyroidism.
Chunmei Li, Eliane Beauregard-Lacroix, Christine Kondratev, Justine Rousseau, Ah Jung Heo, Katherine Neas, Brett H Graham, Jill A Rosenfeld, Carlos A Bacino, Matias Wagner,[...]. Am J Hum Genet 2021
5
40

Mechanisms underlying ubiquitination.
C M Pickart. Annu Rev Biochem 2001
33

OTUD7A Regulates Neurodevelopmental Phenotypes in the 15q13.3 Microdeletion Syndrome.
Mohammed Uddin, Brianna K Unda, Vickie Kwan, Nicholas T Holzapfel, Sean H White, Leon Chalil, Marc Woodbury-Smith, Karen S Ho, Erin Harward, Nadeem Murtaza,[...]. Am J Hum Genet 2018
43
33

USP7 Acts as a Molecular Rheostat to Promote WASH-Dependent Endosomal Protein Recycling and Is Mutated in a Human Neurodevelopmental Disorder.
Yi-Heng Hao, Michael D Fountain, Klementina Fon Tacer, Fan Xia, Weimin Bi, Sung-Hae L Kang, Ankita Patel, Jill A Rosenfeld, Cédric Le Caignec, Bertrand Isidor,[...]. Mol Cell 2015
115
33


Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features.
Jing Zhang, Tomasz Gambin, Bo Yuan, Przemyslaw Szafranski, Jill A Rosenfeld, Mohammed Al Balwi, Abdulrahman Alswaid, Lihadh Al-Gazali, Aisha M Al Shamsi, Makanko Komara,[...]. Hum Genet 2017
23
33

The OTUD5-UBR5 complex regulates FACT-mediated transcription at damaged chromatin.
Angelo de Vivo, Anthony Sanchez, Jose Yegres, Jeonghyeon Kim, Sylvia Emly, Younghoon Kee. Nucleic Acids Res 2019
24
33

Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardation.
Guy Froyen, Mark Corbett, Joke Vandewalle, Irma Jarvela, Owen Lawrence, Cliff Meldrum, Marijke Bauters, Karen Govaerts, Lucianne Vandeleur, Hilde Van Esch,[...]. Am J Hum Genet 2008
159
33

Ubiquitin chain diversity at a glance.
Masato Akutsu, Ivan Dikic, Anja Bremm. J Cell Sci 2016
261
33

Targeted deep resequencing identifies MID2 mutation for X-linked intellectual disability with varied disease severity in a large kindred from India.
Thenral S Geetha, Kulandaimanuvel Antony Michealraj, Madhulika Kabra, Gurjit Kaur, Ramesh C Juyal, B K Thelma. Hum Mutat 2014
26
33

RING-type E3 ligases: master manipulators of E2 ubiquitin-conjugating enzymes and ubiquitination.
Meredith B Metzger, Jonathan N Pruneda, Rachel E Klevit, Allan M Weissman. Biochim Biophys Acta 2014
348
33

Breaking the chains: deubiquitylating enzyme specificity begets function.
Michael J Clague, Sylvie Urbé, David Komander. Nat Rev Mol Cell Biol 2019
259
33

Human USP18 deficiency underlies type 1 interferonopathy leading to severe pseudo-TORCH syndrome.
Marije E C Meuwissen, Rachel Schot, Sofija Buta, Grétel Oudesluijs, Sigrid Tinschert, Scott D Speer, Zhi Li, Leontine van Unen, Daphne Heijsman, Tobias Goldmann,[...]. J Exp Med 2016
153
33

Mutations in USP9X are associated with X-linked intellectual disability and disrupt neuronal cell migration and growth.
Claire C Homan, Raman Kumar, Lam Son Nguyen, Eric Haan, F Lucy Raymond, Fatima Abidi, Martine Raynaud, Charles E Schwartz, Stephen A Wood, Jozef Gecz,[...]. Am J Hum Genet 2014
78
33

Report of the first patient with a homozygous OTUD7A variant responsible for epileptic encephalopathy and related proteasome dysfunction.
Philippine Garret, Frédéric Ebstein, Geoffroy Delplancq, Blandine Dozieres-Puyravel, Aïcha Boughalem, Stéphane Auvin, Yannis Duffourd, Sandro Klafack, Barbara A Zieba, Sana Mahmoudi,[...]. Clin Genet 2020
12
33

New innovations: therapeutic opportunities for intellectual disabilities.
Jonathan D Picker, Christopher A Walsh. Ann Neurol 2013
22
33

Functional Diversification of SRSF Protein Kinase to Control Ubiquitin-Dependent Neurodevelopmental Signaling.
Francisco Bustos, Anna Segarra-Fas, Gino Nardocci, Andrew Cassidy, Odetta Antico, Lindsay Davidson, Lennart Brandenburg, Thomas J Macartney, Rachel Toth, C James Hastie,[...]. Dev Cell 2020
11
33

RNF12 initiates X-chromosome inactivation by targeting REX1 for degradation.
Cristina Gontan, Eskeatnaf Mulugeta Achame, Jeroen Demmers, Tahsin Stefan Barakat, Eveline Rentmeester, Wilfred van IJcken, J Anton Grootegoed, Joost Gribnau. Nature 2012
142
33

Pathogenic variants in E3 ubiquitin ligase RLIM/RNF12 lead to a syndromic X-linked intellectual disability and behavior disorder.
Suzanna G M Frints, Aysegul Ozanturk, Germán Rodríguez Criado, Ute Grasshoff, Bas de Hoon, Michael Field, Sylvie Manouvrier-Hanu, Scott E Hickey, Molka Kammoun, Karen W Gripp,[...]. Mol Psychiatry 2019
14
33

RNF12 X-Linked Intellectual Disability Mutations Disrupt E3 Ligase Activity and Neural Differentiation.
Francisco Bustos, Anna Segarra-Fas, Viduth K Chaugule, Lennart Brandenburg, Emma Branigan, Rachel Toth, Thomas Macartney, Axel Knebel, Ronald T Hay, Helen Walden,[...]. Cell Rep 2018
18
33

X-linked mental retardation.
H-Hilger Ropers, Ben C J Hamel. Nat Rev Genet 2005
329
33

RNF12 controls embryonic stem cell fate and morphogenesis in zebrafish embryos by targeting Smad7 for degradation.
Long Zhang, Huizhe Huang, Fangfang Zhou, Joost Schimmel, Cristina Gontan Pardo, Tingting Zhang, Tahsin Stefan Barakat, Kelly-Ann Sheppard, Craig Mickanin, Jeff A Porter,[...]. Mol Cell 2012
65
33

iPSC modeling of rare pediatric disorders.
Bethany A Freel, Jordan N Sheets, Kevin R Francis. J Neurosci Methods 2020
7
33

Genetic basis of intellectual disability.
Jay W Ellison, Jill A Rosenfeld, Lisa G Shaffer. Annu Rev Med 2013
65
33

Layers of DUB regulation.
Danny D Sahtoe, Titia K Sixma. Trends Biochem Sci 2015
91
33

Mechanisms of Deubiquitinase Specificity and Regulation.
Tycho E T Mevissen, David Komander. Annu Rev Biochem 2017
430
33

Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies.
Michael D Fountain, David S Oleson, Megan E Rech, Lara Segebrecht, Jill V Hunter, John M McCarthy, Philip J Lupo, Manuel Holtgrewe, Rocio Moran, Jill A Rosenfeld,[...]. Genet Med 2019
20
33

Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling.
Brett V Johnson, Raman Kumar, Sabrina Oishi, Suzy Alexander, Maria Kasherman, Michelle Sanchez Vega, Atma Ivancevic, Alison Gardner, Deepti Domingo, Mark Corbett,[...]. Biol Psychiatry 2020
22
33

Clinical whole-exome sequencing for the diagnosis of mendelian disorders.
Yaping Yang, Donna M Muzny, Jeffrey G Reid, Matthew N Bainbridge, Alecia Willis, Patricia A Ward, Alicia Braxton, Joke Beuten, Fan Xia, Zhiyv Niu,[...]. N Engl J Med 2013
16

Combined array CGH plus SNP genome analyses in a single assay for optimized clinical testing.
Joanna Wiszniewska, Weimin Bi, Chad Shaw, Pawel Stankiewicz, Sung-Hae L Kang, Amber N Pursley, Seema Lalani, Patricia Hixson, Tomasz Gambin, Chun-hui Tsai,[...]. Eur J Hum Genet 2014
82
16

Pseudopapilledema and congenital disc anomalies in growth hormone deficiency.
P F Collett-Solberg, G T Liu, M Satin-Smith, L L Katz, T Moshang. J Pediatr Endocrinol Metab 1998
20
16


Molecular findings among patients referred for clinical whole-exome sequencing.
Yaping Yang, Donna M Muzny, Fan Xia, Zhiyv Niu, Richard Person, Yan Ding, Patricia Ward, Alicia Braxton, Min Wang, Christian Buhay,[...]. JAMA 2014
863
16

Fragile X and X-linked intellectual disability: four decades of discovery.
Herbert A Lubs, Roger E Stevenson, Charles E Schwartz. Am J Hum Genet 2012
142
16


Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
16

Next-generation sequencing in X-linked intellectual disability.
Andreas Tzschach, Ute Grasshoff, Stefanie Beck-Woedl, Claudia Dufke, Claudia Bauer, Martin Kehrer, Christina Evers, Ute Moog, Barbara Oehl-Jaschkowitz, Nataliya Di Donato,[...]. Eur J Hum Genet 2015
85
16

Deletions and duplications of developmental pathway genes in 5q31 contribute to abnormal phenotypes.
Jill A Rosenfeld, Joanne Milisa Drautz, Carol L Clericuzio, Tom Cushing, Salmo Raskin, Judith Martin, Raymond C Tervo, Jose A Pitarque, Dorota M Nowak, Justyna A Karolak,[...]. Am J Med Genet A 2011
25
16

Gain-of-Function MN1 Truncation Variants Cause a Recognizable Syndrome with Craniofacial and Brain Abnormalities.
Noriko Miyake, Hidehisa Takahashi, Kazuyuki Nakamura, Bertrand Isidor, Yoko Hiraki, Eriko Koshimizu, Masaaki Shiina, Kazunori Sasaki, Hidefumi Suzuki, Ryota Abe,[...]. Am J Hum Genet 2020
19
16

GeneMatcher: a matching tool for connecting investigators with an interest in the same gene.
Nara Sobreira, François Schiettecatte, David Valle, Ada Hamosh. Hum Mutat 2015
721
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.