A citation-based method for searching scientific literature

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, Claudia P Restrepo Muñeton, George Wehby, Jacqueline T Hecht, Frederic Deleyiannis, Seth M Weinberg, Yah Huei Wu-Chou, Philip K Chen, Harrison Brand, Michael P Epstein, Ingo Ruczinski, Jeffrey C Murray, Terri H Beaty, Eleanor Feingold, Robert J Lipinski, David J Cutler, Mary L Marazita, Elizabeth J Leslie. Am J Hum Genet 2020
Times Cited: 17







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



Times Cited
  Times     Co-cited
Similarity


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
424
47

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
148
47

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
333
41

Mutations in the Epithelial Cadherin-p120-Catenin Complex Cause Mendelian Non-Syndromic Cleft Lip with or without Cleft Palate.
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,[...]. Am J Hum Genet 2018
56
35

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
300
35

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
29

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
127
29

Cleft lip and palate.
Peter A Mossey, Julian Little, Ron G Munger, Mike J Dixon, William C Shaw. Lancet 2009
868
29

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
236
29

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
29

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
47
29

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
29

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
36
29

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
29

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
134
29

A framework for the interpretation of de novo mutation in human disease.
Kaitlin E Samocha, Elise B Robinson, Stephan J Sanders, Christine Stevens, Aniko Sabo, Lauren M McGrath, Jack A Kosmicki, Karola Rehnström, Swapan Mallick, Andrew Kirby,[...]. Nat Genet 2014
579
23

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
580
23

Genetic factors define CPO and CLO subtypes of nonsyndromicorofacial cleft.
Lulin Huang, Zhonglin Jia, Yi Shi, Qin Du, Jiayu Shi, Ziyan Wang, Yandong Mou, Qingwei Wang, Bihe Zhang, Qing Wang,[...]. PLoS Genet 2019
41
23

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
23

Genetics of cleft lip and cleft palate.
Elizabeth J Leslie, Mary L Marazita. Am J Med Genet C Semin Med Genet 2013
227
23

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
28
23

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
159
23

Non-Syndromic Cleft Lip with or without Cleft Palate: Genome-Wide Association Study in Europeans Identifies a Suggestive Risk Locus at 16p12.1 and Supports SH3PXD2A as a Clefting Susceptibility Gene.
Iris Alm van Rooij, Kerstin U Ludwig, Julia Welzenbach, Nina Ishorst, Michelle Thonissen, Tessel E Galesloot, Edwin Ongkosuwito, Stefaan J Bergé, Khalid Aldhorae, Augusto Rojas-Martinez,[...]. Genes (Basel) 2019
15
26

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
87
23

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
28
23

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
783
17

De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies.
Jason Homsy, Samir Zaidi, Yufeng Shen, James S Ware, Kaitlin E Samocha, Konrad J Karczewski, Steven R DePalma, David McKean, Hiroko Wakimoto, Josh Gorham,[...]. Science 2015
425
17

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
428
17

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
58
17

Identification of common non-coding variants at 1p22 that are functional for non-syndromic orofacial clefting.
Huan Liu, Elizabeth J Leslie, Jenna C Carlson, Terri H Beaty, Mary L Marazita, Andrew C Lidral, Robert A Cornell. Nat Commun 2017
39
17

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
101
17

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
69
17

Confirming genes influencing risk to cleft lip with/without cleft palate in a case-parent trio study.
T H Beaty, M A Taub, A F Scott, J C Murray, M L Marazita, H Schwender, M M Parker, J B Hetmanski, P Balakrishnan, M A Mansilla,[...]. Hum Genet 2013
102
17


High-Resolution Epigenomic Atlas of Human Embryonic Craniofacial Development.
Andrea Wilderman, Jennifer VanOudenhove, Jeffrey Kron, James P Noonan, Justin Cotney. Cell Rep 2018
59
17


Toward an orofacial gene regulatory network.
Youssef A Kousa, Brian C Schutte. Dev Dyn 2016
43
17

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
18

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
50
17

Disease gene identification strategies for exome sequencing.
Christian Gilissen, Alexander Hoischen, Han G Brunner, Joris A Veltman. Eur J Hum Genet 2012
290
11

DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources.
Helen V Firth, Shola M Richards, A Paul Bevan, Stephen Clayton, Manuel Corpas, Diana Rajan, Steven Van Vooren, Yves Moreau, Roger M Pettett, Nigel P Carter. Am J Hum Genet 2009
11

The mutational constraint spectrum quantified from variation in 141,456 humans.
Konrad J Karczewski, Laurent C Francioli, Grace Tiao, Beryl B Cummings, Jessica Alföldi, Qingbo Wang, Ryan L Collins, Kristen M Laricchia, Andrea Ganna, Daniel P Birnbaum,[...]. Nature 2020
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

Genome sequencing identifies major causes of severe intellectual disability.
Christian Gilissen, Jayne Y Hehir-Kwa, Djie Tjwan Thung, Maartje van de Vorst, Bregje W M van Bon, Marjolein H Willemsen, Michael Kwint, Irene M Janssen, Alexander Hoischen, Annette Schenck,[...]. Nature 2014
710
11

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data.
Kai Wang, Mingyao Li, Hakon Hakonarson. Nucleic Acids Res 2010
11

The Sequence Alignment/Map format and SAMtools.
Heng Li, Bob Handsaker, Alec Wysoker, Tim Fennell, Jue Ruan, Nils Homer, Gabor Marth, Goncalo Abecasis, Richard Durbin. Bioinformatics 2009
11

Patterns and rates of exonic de novo mutations in autism spectrum disorders.
Benjamin M Neale, Yan Kou, Li Liu, Avi Ma'ayan, Kaitlin E Samocha, Aniko Sabo, Chiao-Feng Lin, Christine Stevens, Li-San Wang, Vladimir Makarov,[...]. Nature 2012
11

Comparison and integration of deleteriousness prediction methods for nonsynonymous SNVs in whole exome sequencing studies.
Chengliang Dong, Peng Wei, Xueqiu Jian, Richard Gibbs, Eric Boerwinkle, Kai Wang, Xiaoming Liu. Hum Mol Genet 2015
609
11

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.
Brian J O'Roak, Laura Vives, Santhosh Girirajan, Emre Karakoc, Niklas Krumm, Bradley P Coe, Roie Levy, Arthur Ko, Choli Lee, Joshua D Smith,[...]. Nature 2012
11

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
11


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.