A citation-based method for searching scientific literature

K Osoegawa, G M Vessere, K H Utami, M A Mansilla, M K Johnson, B M Riley, J L'Heureux, R Pfundt, J Staaf, W A van der Vliet, A C Lidral, E F P M Schoenmakers, A Borg, B C Schutte, E J Lammer, J C Murray, P J de Jong. J Med Genet 2008
Times Cited: 71







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



Times Cited
  Times     Co-cited
Similarity


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
414
29

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
559
26

Impaired FGF signaling contributes to cleft lip and palate.
Bridget M Riley, M Adela Mansilla, Jinghong Ma, Sandra Daack-Hirsch, Brion S Maher, Lisa M Raffensperger, Erilynn T Russo, Alexandre R Vieira, Catherine Dodé, Moosa Mohammadi,[...]. Proc Natl Acad Sci U S A 2007
192
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
855
21

Cleft lip and palate.
Peter A Mossey, Julian Little, Ron G Munger, Mike J Dixon, William C Shaw. Lancet 2009
744
19

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
384
18


Medical sequencing of candidate genes for nonsyndromic cleft lip and palate.
Alexandre R Vieira, Joseph R Avila, Sandra Daack-Hirsch, Ecaterina Dragan, Têmis M Félix, Fedik Rahimov, Jill Harrington, Rebecca R Schultz, Yoriko Watanabe, Marla Johnson,[...]. PLoS Genet 2005
179
15

Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate.
P A Jezewski, A R Vieira, C Nishimura, B Ludwig, M Johnson, S E O'Brien, S Daack-Hirsch, R E Schultz, A Weber, B Nepomucena,[...]. J Med Genet 2003
204
15

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
303
15


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
272
15

SUMO1 haploinsufficiency leads to cleft lip and palate.
Fowzan S Alkuraya, Irfan Saadi, Jennifer J Lund, Annick Turbe-Doan, Cynthia C Morton, Richard L Maas. Science 2006
136
14

MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans.
M J van den Boogaard, M Dorland, F A Beemer, H K van Amstel. Nat Genet 2000
409
14

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
308
14

De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot.
Steven C Greenway, Alexandre C Pereira, Jennifer C Lin, Steven R DePalma, Samuel J Israel, Sonia M Mesquita, Emel Ergul, Jessie H Conta, Joshua M Korn, Steven A McCarroll,[...]. Nat Genet 2009
296
14


Orofacial clefting: recent insights into a complex trait.
Astanand Jugessur, Jeffrey C Murray. Curr Opin Genet Dev 2005
157
12


Identification of SATB2 as the cleft palate gene on 2q32-q33.
David R FitzPatrick, Ian M Carr, Lorna McLaren, Jack P Leek, Patrick Wightman, Kathy Williamson, Philippe Gautier, Niolette McGill, Caroline Hayward, Helen Firth,[...]. Hum Mol Genet 2003
188
12

Identification of microdeletions in candidate genes for cleft lip and/or palate.
Min Shi, Adrianna Mostowska, Astanand Jugessur, Marla K Johnson, Maria Adela Mansilla, Kaare Christensen, Rolv T Lie, Allen J Wilcox, Jeffrey C Murray. Birth Defects Res A Clin Mol Teratol 2009
38
23

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
214
12

Association of MSX1 and TGFB3 with nonsyndromic clefting in humans.
A C Lidral, P A Romitti, A M Basart, T Doetschman, N J Leysens, S Daack-Hirsch, E V Semina, L R Johnson, J Machida, A Burds,[...]. Am J Hum Genet 1998
236
11


Disruption of Fgf10/Fgfr2b-coordinated epithelial-mesenchymal interactions causes cleft palate.
Ritva Rice, Bradley Spencer-Dene, Elaine C Connor, Amel Gritli-Linde, Andrew P McMahon, Clive Dickson, Irma Thesleff, David P C Rice. J Clin Invest 2004
257
11

TFAP2A mutations result in branchio-oculo-facial syndrome.
Jeff M Milunsky, Tom A Maher, Geping Zhao, Amy E Roberts, Heather J Stalker, Roberto T Zori, Michelle N Burch, Michele Clemens, John B Mulliken, Rosemarie Smith,[...]. Am J Hum Genet 2008
132
11

Development of the upper lip: morphogenetic and molecular mechanisms.
Rulang Jiang, Jeffrey O Bush, Andrew C Lidral. Dev Dyn 2006
184
11

Association between IRF6 and nonsyndromic cleft lip with or without cleft palate in four populations.
Ji Wan Park, Iain McIntosh, Jacqueline B Hetmanski, Ethylin Wang Jabs, Craig A Vander Kolk, Yah-Huei Wu-Chou, Philip K Chen, Samuel S Chong, Vincent Yeow, Sun Ha Jee,[...]. Genet Med 2007
77
11

Global variation in copy number in the human genome.
Richard Redon, Shumpei Ishikawa, Karen R Fitch, Lars Feuk, George H Perry, T Daniel Andrews, Heike Fiegler, Michael H Shapero, Andrew R Carson, Wenwei Chen,[...]. Nature 2006
11

Genome scan, fine-mapping, and candidate gene analysis of non-syndromic cleft lip with or without cleft palate reveals phenotype-specific differences in linkage and association results.
Mary L Marazita, Andrew C Lidral, Jeffrey C Murray, L Leigh Field, Brion S Maher, Toby Goldstein McHenry, Margaret E Cooper, Manika Govil, Sandra Daack-Hirsch, Bridget Riley,[...]. Hum Hered 2009
88
11

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
194
11

Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities.
Nicola Brunetti-Pierri, Jonathan S Berg, Fernando Scaglia, John Belmont, Carlos A Bacino, Trilochan Sahoo, Seema R Lalani, Brett Graham, Brendan Lee, Marwan Shinawi,[...]. Nat Genet 2008
389
11


Role of TBX1 in human del22q11.2 syndrome.
Hisato Yagi, Yoshiyuki Furutani, Hiromichi Hamada, Takashi Sasaki, Shuichi Asakawa, Shinsei Minoshima, Fukiko Ichida, Kunitaka Joo, Misa Kimura, Shin-ichiro Imamura,[...]. Lancet 2003
523
9

Mutations in a new member of the chromodomain gene family cause CHARGE syndrome.
Lisenka E L M Vissers, Conny M A van Ravenswaaij, Ronald Admiraal, Jane A Hurst, Bert B A de Vries, Irene M Janssen, Walter A van der Vliet, Erik H L P G Huys, Pieter J de Jong, Ben C J Hamel,[...]. Nat Genet 2004
756
9

Strong evidence of linkage disequilibrium between polymorphisms at the IRF6 locus and nonsyndromic cleft lip with or without cleft palate, in an Italian population.
Luca Scapoli, Annalisa Palmieri, Marcella Martinelli, Furio Pezzetti, Paolo Carinci, Mauro Tognon, Francesco Carinci. Am J Hum Genet 2005
114
9

Mutations of PVRL1, encoding a cell-cell adhesion molecule/herpesvirus receptor, in cleft lip/palate-ectodermal dysplasia.
K Suzuki, D Hu, T Bustos, J Zlotogora, A Richieri-Costa, J A Helms, R A Spritz. Nat Genet 2000
239
9

Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome.
J Celli, P Duijf, B C Hamel, M Bamshad, B Kramer, A P Smits, R Newbury-Ecob, R C Hennekam, G Van Buggenhout, A van Haeringen,[...]. Cell 1999
521
9

Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.
Catherine Dodé, Jacqueline Levilliers, Jean-Michel Dupont, Anne De Paepe, Nathalie Le Dû, Nadia Soussi-Yanicostas, Roney S Coimbra, Sedigheh Delmaghani, Sylvie Compain-Nouaille, Françoise Baverel,[...]. Nat Genet 2003
503
9

Genetic variants in IRF6 and the risk of facial clefts: single-marker and haplotype-based analyses in a population-based case-control study of facial clefts in Norway.
Astanand Jugessur, Fedik Rahimov, Rolv T Lie, Allen J Wilcox, Håkon K Gjessing, Roy M Nilsen, Truc Trung Nguyen, Jeffrey C Murray. Genet Epidemiol 2008
69
10

Lip pits and deletion 1q32----41.
M Bocian, A P Walker. Am J Med Genet 1987
71
9


Interferon regulatory factor-6: a gene predisposing to isolated cleft lip with or without cleft palate in the Belgian population.
Michella Ghassibé, Benedicte Bayet, Nicole Revencu, Christine Verellen-Dumoulin, Yves Gillerot, Romain Vanwijck, Miikka Vikkula. Eur J Hum Genet 2005
68
10

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
105
9

Genetic determinants of facial clefting: analysis of 357 candidate genes using two national cleft studies from Scandinavia.
Astanand Jugessur, Min Shi, Håkon Kristian Gjessing, Rolv Terje Lie, Allen James Wilcox, Clarice Ring Weinberg, Kaare Christensen, Abee Lowman Boyles, Sandra Daack-Hirsch, Truc Nguyen Trung,[...]. PLoS One 2009
74
9

Mutations in BMP4 are associated with subepithelial, microform, and overt cleft lip.
Satoshi Suzuki, Mary L Marazita, Margaret E Cooper, Nobutomo Miwa, Anne Hing, Astanand Jugessur, Nagato Natsume, Kazuo Shimozato, Naofumi Ohbayashi, Yasushi Suzuki,[...]. Am J Hum Genet 2009
140
9


A copy number variation morbidity map of developmental delay.
Gregory M Cooper, Bradley P Coe, Santhosh Girirajan, Jill A Rosenfeld, Tiffany H Vu, Carl Baker, Charles Williams, Heather Stalker, Rizwan Hamid, Vickie Hannig,[...]. Nat Genet 2011
803
9

PVRL1 variants contribute to non-syndromic cleft lip and palate in multiple populations.
Joseph R Avila, Peter A Jezewski, Alexandre R Vieira, Iêda M Orioli, Eduardo E Castilla, Kaare Christensen, Sandra Daack-Hirsch, Paul A Romitti, Jeffrey C Murray. Am J Med Genet A 2006
57
10

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
117
8


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.