A citation-based method for searching scientific literature

Sandra Jansen, Ilse M van der Werf, A Micheil Innes, Alexandra Afenjar, Pankaj B Agrawal, Ilse J Anderson, Paldeep S Atwal, Ellen van Binsbergen, Marie-José van den Boogaard, Lucia Castiglia, Zeynep H Coban-Akdemir, Anke van Dijck, Diane Doummar, Albertien M van Eerde, Anthonie J van Essen, Koen L van Gassen, Maria J Guillen Sacoto, Mieke M van Haelst, Ivan Iossifov, Jessica L Jackson, Elizabeth Judd, Charu Kaiwar, Boris Keren, Eric W Klee, Jolien S Klein Wassink-Ruiter, Marije E Meuwissen, Kristin G Monaghan, Sonja A de Munnik, Caroline Nava, Charlotte W Ockeloen, Rosa Pettinato, Hilary Racher, Tuula Rinne, Corrado Romano, Victoria R Sanders, Rhonda E Schnur, Eric J Smeets, Alexander P A Stegmann, Asbjørg Stray-Pedersen, David A Sweetser, Paulien A Terhal, Kristian Tveten, Grace E VanNoy, Petra F de Vries, Jessica L Waxler, Marcia Willing, Rolph Pfundt, Joris A Veltman, R Frank Kooy, Lisenka E L M Vissers, Bert B A de Vries. Eur J Hum Genet 2019
Times Cited: 8







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



Times Cited
  Times     Co-cited
Similarity


De Novo Variants in the F-Box Protein FBXO11 in 20 Individuals with a Variable Neurodevelopmental Disorder.
Anne Gregor, Lynette G Sadleir, Reza Asadollahi, Silvia Azzarello-Burri, Agatino Battaglia, Lilian Bomme Ousager, Paranchai Boonsawat, Ange-Line Bruel, Rebecca Buchert, Eduardo Calpena,[...]. Am J Hum Genet 2018
15
50

De novo FBXO11 mutations are associated with intellectual disability and behavioural anomalies.
Daniel Fritzen, Alma Kuechler, Mona Grimmel, Jessica Becker, Sophia Peters, Marc Sturm, Hela Hundertmark, Axel Schmidt, Martina Kreiß, Tim M Strom,[...]. Hum Genet 2018
15
50

Systematic analysis and nomenclature of mammalian F-box proteins.
Jianping Jin, Timothy Cardozo, Ruth C Lovering, Stephen J Elledge, Michele Pagano, J Wade Harper. Genes Dev 2004
493
37

High diagnostic yield of syndromic intellectual disability by targeted next-generation sequencing.
Francisco Martínez, Alfonso Caro-Llopis, Mónica Roselló, Silvestre Oltra, Sonia Mayo, Sandra Monfort, Carmen Orellana. J Med Genet 2017
56
37

The contribution of de novo coding mutations to autism spectrum disorder.
Ivan Iossifov, Brian J O'Roak, Stephan J Sanders, Michael Ronemus, Niklas Krumm, Dan Levy, Holly A Stessman, Kali T Witherspoon, Laura Vives, Karynne E Patterson,[...]. Nature 2014
25

Analysis of protein-coding genetic variation in 60,706 humans.
Monkol Lek, Konrad J Karczewski, Eric V Minikel, Kaitlin E Samocha, Eric Banks, Timothy Fennell, Anne H O'Donnell-Luria, James S Ware, Andrew J Hill, Beryl B Cummings,[...]. Nature 2016
25

Function and regulation of cullin-RING ubiquitin ligases.
Matthew D Petroski, Raymond J Deshaies. Nat Rev Mol Cell Biol 2005
25

FBXO11 inactivation leads to abnormal germinal-center formation and lymphoproliferative disease.
Christof Schneider, Ning Kon, Letizia Amadori, Qiong Shen, Friederike H Schwartz, Benjamin Tischler, Marion Bossennec, David Dominguez-Sola, Govind Bhagat, Wei Gu,[...]. Blood 2016
28
25

Ubiquitin modifications.
Kirby N Swatek, David Komander. Cell Res 2016
592
25

FBXO11 targets BCL6 for degradation and is inactivated in diffuse large B-cell lymphomas.
Shanshan Duan, Lukas Cermak, Julia K Pagan, Mario Rossi, Cinzia Martinengo, Paola Francia di Celle, Bjoern Chapuy, Margaret Shipp, Roberto Chiarle, Michele Pagano. Nature 2012
177
25

Variable brain phenotype primarily affects the brainstem and cerebellum in patients with osteogenesis imperfecta caused by recessive WNT1 mutations.
Kimberly A Aldinger, Nancy J Mendelsohn, Brian Hy Chung, Wenjuan Zhang, Daniel H Cohn, Bridget Fernandez, Fowzan S Alkuraya, William B Dobyns, Cynthia J Curry. J Med Genet 2016
27
12





Clinical findings in patients with GLI2 mutations--phenotypic variability.
C D P Bertolacini, L A Ribeiro-Bicudo, A Petrin, A Richieri-Costa, J C Murray. Clin Genet 2012
38
12

Compensatory growth renders Tcf7l1a dispensable for eye formation despite its requirement in eye field specification.
Rodrigo M Young, Thomas A Hawkins, Florencia Cavodeassi, Heather L Stickney, Quenten Schwarz, Lisa M Lawrence, Claudia Wierzbicki, Bowie Yl Cheng, Jingyuan Luo, Elizabeth Mayela Ambrosio,[...]. Elife 2019
6
16

beta-catenin is a target for the ubiquitin-proteasome pathway.
H Aberle, A Bauer, J Stappert, A Kispert, R Kemler. EMBO J 1997
12


Genic intolerance to functional variation and the interpretation of personal genomes.
Slavé Petrovski, Quanli Wang, Erin L Heinzen, Andrew S Allen, David B Goldstein. PLoS Genet 2013
561
12

Structure of a beta-TrCP1-Skp1-beta-catenin complex: destruction motif binding and lysine specificity of the SCF(beta-TrCP1) ubiquitin ligase.
Geng Wu, Guozhou Xu, Brenda A Schulman, Philip D Jeffrey, J Wade Harper, Nikola P Pavletich. Mol Cell 2003
477
12


SOX2: Not always eye malformations. Severe genital but no major ocular anomalies in a female patient with the recurrent c.70del20 variant.
Edoardo Errichiello, Cristina Gorgone, Loretta Giuliano, Barbara Iadarola, Emanuela Cosentino, Marzia Rossato, Nehir Edibe Kurtas, Massimo Delledonne, Teresa Mattina, Orsetta Zuffardi. Eur J Med Genet 2018
10
12

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
589
12

LRP4 mutations alter Wnt/beta-catenin signaling and cause limb and kidney malformations in Cenani-Lenz syndrome.
Yun Li, Barbara Pawlik, Nursel Elcioglu, Mona Aglan, Hülya Kayserili, Gökhan Yigit, Ferda Percin, Frances Goodman, Gudrun Nürnberg, Asim Cenani,[...]. Am J Hum Genet 2010
104
12

Genetic compensation: A phenomenon in search of mechanisms.
Mohamed A El-Brolosy, Didier Y R Stainier. PLoS Genet 2017
283
12


Conditional mutations of beta-catenin and APC reveal roles for canonical Wnt signaling in lens differentiation.
Gemma Martinez, Mary Wijesinghe, Kirsty Turner, Helen E Abud, Makoto M Taketo, Tetsuo Noda, Michael L Robinson, Robb U de Iongh. Invest Ophthalmol Vis Sci 2009
38
12

Loss of Axin2 Causes Ocular Defects During Mouse Eye Development.
Ashley Alldredge, Sabine Fuhrmann. Invest Ophthalmol Vis Sci 2016
13
12

Functional Dysregulation of CDC42 Causes Diverse Developmental Phenotypes.
Simone Martinelli, Oliver H F Krumbach, Francesca Pantaleoni, Simona Coppola, Ehsan Amin, Luca Pannone, Kazem Nouri, Luciapia Farina, Radovan Dvorsky, Francesca Lepri,[...]. Am J Hum Genet 2018
66
12

WNT/β-Catenin Signaling in Vertebrate Eye Development.
Naoko Fujimura. Front Cell Dev Biol 2016
44
12

Sonic hedgehog mutations are an uncommon cause of developmental eye anomalies.
Preeti Bakrania, Sibel A Ugur Iseri, Alexander W Wyatt, Dave J Bunyan, Wayne W K Lam, Alison Salt, Jacqueline Ramsay, David O Robinson, Nicola K Ragge. Am J Med Genet A 2010
24
12

Targeted resequencing identifies PTCH1 as a major contributor to ocular developmental anomalies and extends the SOX2 regulatory network.
Nicolas Chassaing, Erica E Davis, Kelly L McKnight, Adrienne R Niederriter, Alexandre Causse, Véronique David, Annaïck Desmaison, Sophie Lamarre, Catherine Vincent-Delorme, Laurent Pasquier,[...]. Genome Res 2016
23
12

Exploring the Wnt signaling pathway in schizophrenia and bipolar disorder.
Eva Z Hoseth, Florian Krull, Ingrid Dieset, Ragni H Mørch, Sigrun Hope, Erlend S Gardsjord, Nils Eiel Steen, Ingrid Melle, Hans-Richard Brattbakk, Vidar M Steen,[...]. Transl Psychiatry 2018
43
12

Repressor activity of Headless/Tcf3 is essential for vertebrate head formation.
C H Kim, T Oda, M Itoh, D Jiang, K B Artinger, S C Chandrasekharappa, W Driever, A B Chitnis. Nature 2000
307
12

Genetic compensation triggered by mutant mRNA degradation.
Mohamed A El-Brolosy, Zacharias Kontarakis, Andrea Rossi, Carsten Kuenne, Stefan Günther, Nana Fukuda, Khrievono Kikhi, Giulia L M Boezio, Carter M Takacs, Shih-Lei Lai,[...]. Nature 2019
303
12

The Wnt/beta-catenin pathway regulates cardiac valve formation.
Adam F L Hurlstone, Anna-Pavlina G Haramis, Erno Wienholds, Harry Begthel, Jeroen Korving, Fredericus Van Eeden, Edwin Cuppen, Danica Zivkovic, Ronald H A Plasterk, Hans Clevers. Nature 2003
310
12

GLI2 mutations in four Brazilian patients: how wide is the phenotypic spectrum?
Fedik Rahimov, Lucilene Arilho Ribeiro, Eziquiel de Miranda, Antonio Richieri-Costa, Jeffrey C Murray. Am J Med Genet A 2006
42
12


Copy-number variants and candidate gene mutations in isolated split hand/foot malformation.
Tonia C Carter, Robert J Sicko, Denise M Kay, Marilyn L Browne, Paul A Romitti, Zoё L Edmunds, Aiyi Liu, Ruzong Fan, Charlotte M Druschel, Michele Caggana,[...]. J Hum Genet 2017
10
12

Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutations.
Jennifer J Johnston, Julie C Sapp, Joyce T Turner, David Amor, Salim Aftimos, Kyrieckos A Aleck, Maureen Bocian, Joann N Bodurtha, Gerald F Cox, Cynthia J Curry,[...]. Hum Mutat 2010
72
12

Distribution and intensity of constraint in mammalian genomic sequence.
Gregory M Cooper, Eric A Stone, George Asimenos, Eric D Green, Serafim Batzoglou, Arend Sidow. Genome Res 2005
849
12


Synaptic, transcriptional and chromatin genes disrupted in autism.
Silvia De Rubeis, Xin He, Arthur P Goldberg, Christopher S Poultney, Kaitlin Samocha, A Erucment Cicek, Yan Kou, Li Liu, Menachem Fromer, Susan Walker,[...]. Nature 2014
12

Genetic compensation induced by deleterious mutations but not gene knockdowns.
Andrea Rossi, Zacharias Kontarakis, Claudia Gerri, Hendrik Nolte, Soraya Hölper, Marcus Krüger, Didier Y R Stainier. Nature 2015
647
12

How Wnt Signaling Builds the Brain: Bridging Development and Disease.
Rivka Noelanders, Kris Vleminckx. Neuroscientist 2017
39
12

Molecular and clinical spectra of FBXL4 deficiency.
Ayman W El-Hattab, Hongzheng Dai, Mohammed Almannai, Julia Wang, Eissa A Faqeih, Ali Al Asmari, Mohammed A M Saleh, Mohammed A O Elamin, Majid Alfadhel, Fowzan S Alkuraya,[...]. Hum Mutat 2017
21
12

The β-catenin destruction complex.
Jennifer L Stamos, William I Weis. Cold Spring Harb Perspect Biol 2013
517
12

Communicating with Hedgehogs.
Joan E Hooper, Matthew P Scott. Nat Rev Mol Cell Biol 2005
615
12

High-resolution in situ hybridization to whole-mount zebrafish embryos.
Christine Thisse, Bernard Thisse. Nat Protoc 2008
12


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.