A citation-based method for searching scientific literature

Liza L Cox, Timothy C Cox, Lina M Moreno Uribe, Ying Zhu, Chika T Richter, Nichole Nidey, Jennifer M Standley, Mei Deng, Elizabeth Blue, Jessica X Chong, Yueqin Yang, Russ P Carstens, Deepti Anand, Salil A Lachke, Joshua D Smith, Michael O Dorschner, Bruce Bedell, Edwin Kirk, Anne V Hing, Hanka Venselaar, Luz C Valencia-Ramirez, Michael J Bamshad, Ian A Glass, Jonathan A Cooper, Eric Haan, Deborah A Nickerson, Hans van Bokhoven, Huiqing Zhou, Katy N Krahn, Michael F Buckley, Jeffrey C Murray, Andrew C Lidral, Tony Roscioli. Am J Hum Genet 2018
Times Cited: 60







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



Times Cited
  Times     Co-cited
Similarity


Cleft lip and palate: understanding genetic and environmental influences.
Michael J Dixon, Mary L Marazita, Terri H Beaty, Jeffrey C Murray. Nat Rev Genet 2011
45

Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity.
Yanqin Yu, Xianbo Zuo, Miao He, Jinping Gao, Yuchuan Fu, Chuanqi Qin, Liuyan Meng, Wenjun Wang, Yaling Song, Yong Cheng,[...]. Nat Commun 2017
153
41

A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4.
Terri H Beaty, Jeffrey C Murray, Mary L Marazita, Ronald G Munger, Ingo Ruczinski, Jacqueline B Hetmanski, Kung Yee Liang, Tao Wu, Tanda Murray, M Daniele Fallin,[...]. Nat Genet 2010
425
30

Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts.
Alexandre Bureau, Margaret M Parker, Ingo Ruczinski, Margaret A Taub, Mary L Marazita, Jeffrey C Murray, Elisabeth Mangold, Markus M Noethen, Kirsten U Ludwig, Jacqueline B Hetmanski,[...]. Genetics 2014
56
32

Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate.
Elisabeth Mangold, Kerstin U Ludwig, Stefanie Birnbaum, Carlotta Baluardo, Melissa Ferrian, Stefan Herms, Heiko Reutter, Nilma Almeida de Assis, Taofik Al Chawa, Manuel Mattheisen,[...]. Nat Genet 2010
302
28

Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24.
Stefanie Birnbaum, Kerstin U Ludwig, Heiko Reutter, Stefan Herms, Michael Steffens, Michele Rubini, Carlotta Baluardo, Melissa Ferrian, Nilma Almeida de Assis, Margrieta A Alblas,[...]. Nat Genet 2009
334
26

Genome-wide association study identifies a new susceptibility locus for cleft lip with or without a cleft palate.
Yimin Sun, Yongqing Huang, Aihua Yin, Yongchu Pan, Yirui Wang, Cheng Wang, Yong Du, Meilin Wang, Feifei Lan, Zhibin Hu,[...]. Nat Commun 2015
135
23

Whole exome sequencing identifies mutations in 10% of patients with familial non-syndromic cleft lip and/or palate in genes mutated in well-known syndromes.
Mirta Basha, Bénédicte Demeer, Nicole Revencu, Raphael Helaers, Stephanie Theys, Sami Bou Saba, Odile Boute, Bernard Devauchelle, Geneviève Francois, Bénédicte Bayet,[...]. J Med Genet 2018
51
27

Cleft lip and palate.
Peter A Mossey, Julian Little, Ron G Munger, Mike J Dixon, William C Shaw. Lancet 2009
882
21

Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.
Kerstin U Ludwig, Elisabeth Mangold, Stefan Herms, Stefanie Nowak, Heiko Reutter, Anna Paul, Jessica Becker, Ruth Herberz, Taofik AlChawa, Entessar Nasser,[...]. Nat Genet 2012
237
21

Blepharocheilodontic syndrome is a CDH1 pathway-related disorder due to mutations in CDH1 and CTNND1.
Jamal Ghoumid, Morgane Stichelbout, Anne-Sophie Jourdain, Frederic Frenois, Sophie Lejeune-Dumoulin, Marie-Pierre Alex-Cordier, Marine Lebrun, Pierre Guerreschi, Veronique Duquennoy-Martinot, Matthieu Vinchon,[...]. Genet Med 2017
33
39

Imputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip ± cleft palate and cleft palate only.
Kerstin U Ludwig, Anne C Böhmer, John Bowes, Miloš Nikolic, Nina Ishorst, Niki Wyatt, Nigel L Hammond, Lina Gölz, Frederic Thieme, Sandra Barth,[...]. Hum Mol Genet 2017
60
21

Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palate.
Elizabeth J Leslie, Jenna C Carlson, John R Shaffer, Azeez Butali, Carmen J Buxó, Eduardo E Castilla, Kaare Christensen, Fred W B Deleyiannis, L Leigh Field, Jacqueline T Hecht,[...]. Hum Genet 2017
88
18

Rare Variants in the Epithelial Cadherin Gene Underlying the Genetic Etiology of Nonsyndromic Cleft Lip with or without Cleft Palate.
Luciano Abreu Brito, Guilherme Lopes Yamamoto, Soraia Melo, Carolina Malcher, Simone Gomes Ferreira, Joana Figueiredo, Lucas Alvizi, Gerson Shigeru Kobayashi, Michel Satya Naslavsky, Nivaldo Alonso,[...]. Hum Mutat 2015
35
31

Identification of functional variants for cleft lip with or without cleft palate in or near PAX7, FGFR2, and NOG by targeted sequencing of GWAS loci.
Elizabeth J Leslie, Margaret A Taub, Huan Liu, Karyn Meltz Steinberg, Daniel C Koboldt, Qunyuan Zhang, Jenna C Carlson, Jacqueline B Hetmanski, Hang Wang, David E Larson,[...]. Am J Hum Genet 2015
106
18

Exome sequencing provides additional evidence for the involvement of ARHGAP29 in Mendelian orofacial clefting and extends the phenotypic spectrum to isolated cleft palate.
Huan Liu, Tamara Busch, Steven Eliason, Deepti Anand, Steven Bullard, Lord J J Gowans, Nichole Nidey, Aline Petrin, Eno-Abasi Augustine-Akpan, Irfan Saadi,[...]. Birth Defects Res 2017
29
37

A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3.
Elizabeth J Leslie, Huan Liu, Jenna C Carlson, John R Shaffer, Eleanor Feingold, George Wehby, Cecelia A Laurie, Deepti Jain, Cathy C Laurie, Kimberly F Doheny,[...]. Am J Hum Genet 2016
102
16


Cleft lip/palate and CDH1/E-cadherin mutations in families with hereditary diffuse gastric cancer.
T Frebourg, C Oliveira, P Hochain, R Karam, S Manouvrier, C Graziadio, M Vekemans, A Hartmann, S Baert-Desurmont, C Alexandre,[...]. J Med Genet 2006
127
16

Variants in members of the cadherin-catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome.
Anneke Kievit, Federico Tessadori, Hannie Douben, Ingrid Jordens, Madelon Maurice, Jeannette Hoogeboom, Raoul Hennekam, Sheela Nampoothiri, Hülya Kayserili, Marco Castori,[...]. Eur J Hum Genet 2018
19
52

A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13.
Elizabeth J Leslie, Jenna C Carlson, John R Shaffer, Eleanor Feingold, George Wehby, Cecelia A Laurie, Deepti Jain, Cathy C Laurie, Kimberly F Doheny, Toby McHenry,[...]. Hum Mol Genet 2016
129
15

Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm development.
Myriam Peyrard-Janvid, Elizabeth J Leslie, Youssef A Kousa, Tiffany L Smith, Martine Dunnwald, Måns Magnusson, Brian A Lentz, Per Unneberg, Ingegerd Fransson, Hannele K Koillinen,[...]. Am J Hum Genet 2014
145
15

Identification of germline mutations in the cancer predisposing gene CDH1 in patients with orofacial clefts.
Ingrid P Vogelaar, Joana Figueiredo, Iris A L M van Rooij, Joana Simões-Correia, Rachel S van der Post, Soraia Melo, Raquel Seruca, Carine E L Carels, Marjolijn J L Ligtenberg, Nicoline Hoogerbrugge. Hum Mol Genet 2013
43
20

Genomic analyses in African populations identify novel risk loci for cleft palate.
Azeez Butali, Peter A Mossey, Wasiu L Adeyemo, Mekonen A Eshete, Lord J J Gowans, Tamara D Busch, Deepti Jain, Wenjie Yu, Liu Huan, Cecelia A Laurie,[...]. Hum Mol Genet 2019
38
23

Risk of oral clefts in twins.
Dorthe Grosen, Camilla Bille, Inge Petersen, Axel Skytthe, Jacob von Bornemann Hjelmborg, Jacob Krabbe Pedersen, Jeffrey Clark Murray, Kaare Christensen. Epidemiology 2011
71
15

Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios.
Madison R Bishop, Kimberly K Diaz Perez, Miranda Sun, Samantha Ho, Pankaj Chopra, Nandita Mukhopadhyay, Jacqueline B Hetmanski, Margaret A Taub, Lina M Moreno-Uribe, Luz Consuelo Valencia-Ramirez,[...]. Am J Hum Genet 2020
21
42

A genome-wide association study identifies a locus for nonsyndromic cleft lip with or without cleft palate on 8q24.
Struan F A Grant, Kai Wang, Haitao Zhang, Wendy Glaberson, Kiran Annaiah, Cecilia E Kim, Jonathan P Bradfield, Joseph T Glessner, Kelly A Thomas, Maria Garris,[...]. J Pediatr 2009
210
13

Meta-analysis Reveals Genome-Wide Significance at 15q13 for Nonsyndromic Clefting of Both the Lip and the Palate, and Functional Analyses Implicate GREM1 As a Plausible Causative Gene.
Kerstin U Ludwig, Syeda Tasnim Ahmed, Anne C Böhmer, Nasim Bahram Sangani, Sheryil Varghese, Johanna Klamt, Hannah Schuenke, Pinar Gültepe, Andrea Hofmann, Michele Rubini,[...]. PLoS Genet 2016
48
16

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes.
Shinji Kondo, Brian C Schutte, Rebecca J Richardson, Bryan C Bjork, Alexandra S Knight, Yoriko Watanabe, Emma Howard, Renata L L Ferreira de Lima, Sandra Daack-Hirsch, Achim Sander,[...]. Nat Genet 2002
585
13

Development of the upper lip: morphogenetic and molecular mechanisms.
Rulang Jiang, Jeffrey O Bush, Andrew C Lidral. Dev Dyn 2006
205
13



Disruption of an AP-2alpha binding site in an IRF6 enhancer is associated with cleft lip.
Fedik Rahimov, Mary L Marazita, Axel Visel, Margaret E Cooper, Michael J Hitchler, Michele Rubini, Frederick E Domann, Manika Govil, Kaare Christensen, Camille Bille,[...]. Nat Genet 2008
322
13

Mutations in GDF11 and the extracellular antagonist, Follistatin, as a likely cause of Mendelian forms of orofacial clefting in humans.
Timothy C Cox, Andrew C Lidral, Jason C McCoy, Huan Liu, Liza L Cox, Ying Zhu, Ryan D Anderson, Lina M Moreno Uribe, Deepti Anand, Mei Deng,[...]. Hum Mutat 2019
15
53

The molecular anatomy of mammalian upper lip and primary palate fusion at single cell resolution.
Hong Li, Kenneth L Jones, Joan E Hooper, Trevor Williams. Development 2019
30
26

Cleft lip and cleft palate in Esrp1 knockout mice is associated with alterations in epithelial-mesenchymal crosstalk.
SungKyoung Lee, Matthew J Sears, Zijun Zhang, Hong Li, Imad Salhab, Philippe Krebs, Yi Xing, Hyun-Duck Nah, Trevor Williams, Russ P Carstens. Development 2020
16
50

Periderm: Life-cycle and function during orofacial and epidermal development.
Nigel L Hammond, Jill Dixon, Michael J Dixon. Semin Cell Dev Biol 2019
30
23

Periderm prevents pathological epithelial adhesions during embryogenesis.
Rebecca J Richardson, Nigel L Hammond, Pierre A Coulombe, Carola Saloranta, Heidi O Nousiainen, Riitta Salonen, Andrew Berry, Neil Hanley, Denis Headon, Riitta Karikoski,[...]. J Clin Invest 2014
69
11

Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate.
Theresa M Zucchero, Margaret E Cooper, Brion S Maher, Sandra Daack-Hirsch, Buena Nepomuceno, Lucilene Ribeiro, Diana Caprau, Kaare Christensen, Yasushi Suzuki, Junichiro Machida,[...]. N Engl J Med 2004
431
11

Common variants in DLG1 locus are associated with non-syndromic cleft lip with or without cleft palate.
A Mostowska, A Gaczkowska, K Żukowski, K U Ludwig, K K Hozyasz, P Wójcicki, E Mangold, A C Böhmer, S Heilmann-Heimbach, M Knapp,[...]. Clin Genet 2018
24
29

High-Resolution Epigenomic Atlas of Human Embryonic Craniofacial Development.
Andrea Wilderman, Jennifer VanOudenhove, Jeffrey Kron, James P Noonan, Justin Cotney. Cell Rep 2018
61
11

Genetics of cleft lip and cleft palate.
Elizabeth J Leslie, Mary L Marazita. Am J Med Genet C Semin Med Genet 2013
229
11

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
11

Breakthroughs in the genetics of orofacial clefting.
Elisabeth Mangold, Kerstin U Ludwig, Markus M Nöthen. Trends Mol Med 2011
92
11

CADD: predicting the deleteriousness of variants throughout the human genome.
Philipp Rentzsch, Daniela Witten, Gregory M Cooper, Jay Shendure, Martin Kircher. Nucleic Acids Res 2019
11

Impact of rare variants in ARHGAP29 to the etiology of oral clefts: role of loss-of-function vs missense variants.
C P Savastano, L A Brito, Á C Faria, N Setó-Salvia, E Peskett, C M Musso, L Alvizi, S A M Ezquina, C James, GOSgene,[...]. Clin Genet 2017
19
36

Long term follow up study of survival associated with cleft lip and palate at birth.
Kaare Christensen, Knud Juel, Anne Maria Herskind, Jeffrey C Murray. BMJ 2004
161
11

FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate.
Lina M Moreno, Maria Adela Mansilla, Steve A Bullard, Margaret E Cooper, Tamara D Busch, Junichiro Machida, Marla K Johnson, David Brauer, Katherine Krahn, Sandy Daack-Hirsch,[...]. Hum Mol Genet 2009
111
10

Association Studies and Direct DNA Sequencing Implicate Genetic Susceptibility Loci in the Etiology of Nonsyndromic Orofacial Clefts in Sub-Saharan African Populations.
L J J Gowans, W L Adeyemo, M Eshete, P A Mossey, T Busch, B Aregbesola, P Donkor, F K N Arthur, S A Bello, A Martinez,[...]. J Dent Res 2016
34
17

A method and server for predicting damaging missense mutations.
Ivan A Adzhubei, Steffen Schmidt, Leonid Peshkin, Vasily E Ramensky, Anna Gerasimova, Peer Bork, Alexey S Kondrashov, Shamil R Sunyaev. Nat Methods 2010
10


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.