A citation-based method for searching scientific literature

Rachel Soemedi, Ana Topf, Ian J Wilson, Rebecca Darlay, Thahira Rahman, Elise Glen, Darroch Hall, Ni Huang, Jamie Bentham, Shoumo Bhattacharya, Catherine Cosgrove, J David Brook, Javier Granados-Riveron, Kerry Setchfield, Frances Bu'lock, Chris Thornborough, Koenraad Devriendt, Jeroen Breckpot, Michael Hofbeck, Mark Lathrop, Anita Rauch, Gillian M Blue, David S Winlaw, Matthew Hurles, Mauro Santibanez-Koref, Heather J Cordell, Judith A Goodship, Bernard D Keavney. Hum Mol Genet 2012
Times Cited: 72







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



Times Cited
  Times     Co-cited
Similarity


Familial recurrence of congenital heart disease: an overview and review of the literature.
Giulio Calcagni, M Cristina Digilio, Anna Sarkozy, Bruno Dallapiccola, Bruno Marino. Eur J Pediatr 2007
47
6

Enalapril in infants with single ventricle: results of a multicenter randomized trial.
Daphne T Hsu, Victor Zak, Lynn Mahony, Lynn A Sleeper, Andrew M Atz, Jami C Levine, Piers C Barker, Chitra Ravishankar, Brian W McCrindle, Richard V Williams,[...]. Circulation 2010
168
4

Exome analysis of a family with pleiotropic congenital heart disease.
Cammon B Arrington, Steven B Bleyl, Norisada Matsunami, Gabriel D Bonnell, Brith E M Otterud, Douglas C Nielsen, Jeffrey Stevens, Shawn Levy, Mark F Leppert, Neil E Bowles. Circ Cardiovasc Genet 2012
40
7

Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications.
Douglas F Levinson, Jubao Duan, Sang Oh, Kai Wang, Alan R Sanders, Jianxin Shi, Nancy Zhang, Bryan J Mowry, Ann Olincy, Farooq Amin,[...]. Am J Psychiatry 2011
316
4

Strong association of de novo copy number mutations with autism.
Jonathan Sebat, B Lakshmi, Dheeraj Malhotra, Jennifer Troge, Christa Lese-Martin, Tom Walsh, Boris Yamrom, Seungtai Yoon, Alex Krasnitz, Jude Kendall,[...]. Science 2007
4

Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies.
Carolien G F de Kovel, Holger Trucks, Ingo Helbig, Heather C Mefford, Carl Baker, Costin Leu, Christian Kluck, Hiltrud Muhle, Sarah von Spiczak, Philipp Ostertag,[...]. Brain 2010
311
4

PlexinA2 and semaphorin signaling during cardiac neural crest development.
C B Brown, L Feiner, M M Lu, J Li, X Ma, A L Webber, L Jia, J A Raper, J A Epstein. Development 2001
155
4

Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlation.
Seema R Lalani, Arsalan M Safiullah, Susan D Fernbach, Karine G Harutyunyan, Christina Thaller, Leif E Peterson, John D McPherson, Richard A Gibbs, Lisa D White, Margaret Hefner,[...]. Am J Hum Genet 2006
235
4

GATA6 mutations cause human cardiac outflow tract defects by disrupting semaphorin-plexin signaling.
Kazuki Kodo, Tsutomu Nishizawa, Michiko Furutani, Shoichi Arai, Eiji Yamamura, Kunitaka Joo, Takao Takahashi, Rumiko Matsuoka, Hiroyuki Yamagishi. Proc Natl Acad Sci U S A 2009
130
4


Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD.
Anath C Lionel, Jennifer Crosbie, Nicole Barbosa, Tara Goodale, Bhooma Thiruvahindrapuram, Jessica Rickaby, Matthew Gazzellone, Andrew R Carson, Jennifer L Howe, Zhuozhi Wang,[...]. Sci Transl Med 2011
221
4

Characterization and in vivo pharmacological rescue of a Wnt2-Gata6 pathway required for cardiac inflow tract development.
Ying Tian, Lijun Yuan, Ashley M Goss, Tao Wang, Jifu Yang, John J Lepore, Diane Zhou, Robert J Schwartz, Vickas Patel, Ethan David Cohen,[...]. Dev Cell 2010
87
4

Vang-like 2 and noncanonical Wnt signaling in outflow tract development.
Deborah J Henderson, Helen M Phillips, Bill Chaudhry. Trends Cardiovasc Med 2006
55
5

High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications.
Tamim H Shaikh, Xiaowu Gai, Juan C Perin, Joseph T Glessner, Hongbo Xie, Kevin Murphy, Ryan O'Hara, Tracy Casalunovo, Laura K Conlin, Monica D'Arcy,[...]. Genome Res 2009
282
4

Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.
Stephan J Sanders, A Gulhan Ercan-Sencicek, Vanessa Hus, Rui Luo, Michael T Murtha, Daniel Moreno-De-Luca, Su H Chu, Michael P Moreau, Abha R Gupta, Susanne A Thomson,[...]. Neuron 2011
802
4

Diagnostic genome profiling in mental retardation.
Bert B A de Vries, Rolph Pfundt, Martijn Leisink, David A Koolen, Lisenka E L M Vissers, Irene M Janssen, Simon van Reijmersdal, Willy M Nillesen, Erik H L P G Huys, Nicole de Leeuw,[...]. Am J Hum Genet 2005
416
4

Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarrays.
Gregory Costain, Anath C Lionel, Daniele Merico, Pamela Forsythe, Kathryn Russell, Chelsea Lowther, Tracy Yuen, Janice Husted, Dimitri J Stavropoulos, Marsha Speevak,[...]. Hum Mol Genet 2013
83
4

Mutation analysis of AMP-activated protein kinase subunits in inherited cardiomyopathies: implications for kinase function and disease pathogenesis.
Sandra Marisa J Oliveira, Javed Ehtisham, Charles S Redwood, Ingegerd Ostman-Smith, Edward M Blair, Hugh Watkins. J Mol Cell Cardiol 2003
38
7

Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius syndrome.
Eva Klopocki, Harald Schulze, Gabriele Strauss, Claus-Eric Ott, Judith Hall, Fabienne Trotier, Silke Fleischhauer, Lynn Greenhalgh, Ruth A Newbury-Ecob, Luitgard M Neumann,[...]. Am J Hum Genet 2007
198
4


Prenatal diagnosis of an atypical 1q21.1 microdeletion and duplication associated with foetal urogenital abnormalities.
Can Liao, Fang Fu, Cui-Xing Yi, Ru Li, Xin Yang, Qin Xu, Dong-Zhi Li. Gene 2012
6
50

Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family.
Q Y Li, R A Newbury-Ecob, J A Terrett, D I Wilson, A R Curtis, C H Yi, T Gebuhr, P J Bullen, S C Robson, T Strachan,[...]. Nat Genet 1997
648
4

Mutations of the Connexin43 gap-junction gene in patients with heart malformations and defects of laterality.
S H Britz-Cunningham, M M Shah, C W Zuppan, W H Fletcher. N Engl J Med 1995
304
4

Congenital heart disease: current knowledge about causes and inheritance.
Gillian M Blue, Edwin P Kirk, Gary F Sholler, Richard P Harvey, David S Winlaw. Med J Aust 2012
123
4

Mutation analysis of Connexon43 gene in Chinese patients with congenital heart defects.
Binbin Wang, Qiaolian Wen, XiaoDong Xie, Shiguo Liu, Mugen Liu, You Tao, Zhongzhi Li, Peisu Suo, Adong Shen, Jing Wang,[...]. Int J Cardiol 2010
10
30

Transposition of the great vessels in a patient with a 2.9 Mb interstitial deletion of 9q31.1 encompassing the inversin gene: clinical report and review.
Bregje W M van Bon, David A Koolen, Rolph Pfundt, Ineke van der Burgt, Nicole de Leeuw, Bert B A de Vries. Am J Med Genet A 2008
7
42

Disruption of the gene Euchromatin Histone Methyl Transferase1 (Eu-HMTase1) is associated with the 9q34 subtelomeric deletion syndrome.
T Kleefstra, M Smidt, M J G Banning, A R Oudakker, H Van Esch, A P M de Brouwer, W Nillesen, E A Sistermans, B C J Hamel, D de Bruijn,[...]. J Med Genet 2005
118
4

NPHP4 variants are associated with pleiotropic heart malformations.
Vanessa M French, Ingrid M B H van de Laar, Marja W Wessels, Christan Rohe, Jolien W Roos-Hesselink, Guangliang Wang, Ingrid M E Frohn-Mulder, Lies-Anne Severijnen, Bianca M de Graaf, Rachel Schot,[...]. Circ Res 2012
26
11

X-linked situs abnormalities result from mutations in ZIC3.
M Gebbia, G B Ferrero, G Pilia, M T Bassi, A Aylsworth, M Penman-Splitt, L M Bird, J S Bamforth, J Burn, D Schlessinger,[...]. Nat Genet 1997
303
4


Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia.
Carsten Bergmann, Manfred Fliegauf, Nadina Ortiz Brüchle, Valeska Frank, Heike Olbrich, Jan Kirschner, Bernhard Schermer, Ingolf Schmedding, Andreas Kispert, Bettina Kränzlin,[...]. Am J Hum Genet 2008
214
4

Germline gain-of-function mutations in RAF1 cause Noonan syndrome.
M Abdur Razzaque, Tsutomu Nishizawa, Yuta Komoike, Hisato Yagi, Michiko Furutani, Ryunosuke Amo, Mitsuhiro Kamisago, Kazuo Momma, Hiroshi Katayama, Masao Nakagawa,[...]. Nat Genet 2007
316
4

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.
A K Ryan, J A Goodship, D I Wilson, N Philip, A Levy, H Seidel, S Schuffenhauer, H Oechsler, B Belohradsky, M Prieur,[...]. J Med Genet 1997
819
4

Dysregulation of the PDGFRA gene causes inflow tract anomalies including TAPVR: integrating evidence from human genetics and model organisms.
Steven B Bleyl, Yukio Saijoh, Noortje A M Bax, Adriana C Gittenberger-de Groot, Lambertus J Wisse, Susan C Chapman, Jennifer Hunter, Hidetaka Shiratori, Hiroshi Hamada, Shigehito Yamada,[...]. Hum Mol Genet 2010
47
6

Genotype-phenotype correlation in 440 patients with NPHP-related ciliopathies.
Moumita Chaki, Julia Hoefele, Susan J Allen, Gokul Ramaswami, Sabine Janssen, Carsten Bergmann, John R Heckenlively, Edgar A Otto, Friedhelm Hildebrandt. Kidney Int 2011
70
4

NOTCH1 mutations in individuals with left ventricular outflow tract malformations reduce ligand-induced signaling.
Kim L McBride, Maurisa F Riley, Gloria A Zender, Sara M Fitzgerald-Butt, Jeffrey A Towbin, John W Belmont, Susan E Cole. Hum Mol Genet 2008
123
4

Missense mutations in CRELD1 are associated with cardiac atrioventricular septal defects.
Susan W Robinson, Cynthia D Morris, Elizabeth Goldmuntz, Mark D Reller, Melanie A Jones, Robert D Steiner, Cheryl L Maslen. Am J Hum Genet 2003
115
4

Alpha-cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects.
Javier T Granados-Riveron, Tushar K Ghosh, Mark Pope, Frances Bu'Lock, Christopher Thornborough, Jacqueline Eason, Edwin P Kirk, Diane Fatkin, Michael P Feneley, Richard P Harvey,[...]. Hum Mol Genet 2010
81
4

Transcription factor pathways and congenital heart disease.
David J McCulley, Brian L Black. Curr Top Dev Biol 2012
181
4

Clinical and molecular delineation of the 17q21.31 microdeletion syndrome.
D A Koolen, A J Sharp, J A Hurst, H V Firth, S J L Knight, A Goldenberg, P Saugier-Veber, R Pfundt, L E L M Vissers, A Destrée,[...]. J Med Genet 2008
150
4

Heterozygous germline mutations in the CBL tumor-suppressor gene cause a Noonan syndrome-like phenotype.
Simone Martinelli, Alessandro De Luca, Emilia Stellacci, Cesare Rossi, Saula Checquolo, Francesca Lepri, Viviana Caputo, Marianna Silvano, Francesco Buscherini, Federica Consoli,[...]. Am J Hum Genet 2010
147
4

Identification and functional analysis of CITED2 mutations in patients with congenital heart defects.
Silke Sperling, Christina H Grimm, Ilona Dunkel, Siegrun Mebus, Hans-Peter Sperling, Arno Ebner, Raffaello Galli, Hans Lehrach, Christoph Fusch, Felix Berger,[...]. Hum Mutat 2005
82
4

Cited2 controls left-right patterning and heart development through a Nodal-Pitx2c pathway.
Simon D Bamforth, José Bragança, Cassandra R Farthing, Jürgen E Schneider, Carol Broadbent, Anna C Michell, Kieran Clarke, Stefan Neubauer, Dominic Norris, Nigel A Brown,[...]. Nat Genet 2004
153
4

Congenital heart defects in Kabuki syndrome.
M C Digilio, B Marino, A Toscano, A Giannotti, B Dallapiccola. Am J Med Genet 2001
73
4

Mutations in the human Jagged1 gene are responsible for Alagille syndrome.
T Oda, A G Elkahloun, B L Pike, K Okajima, I D Krantz, A Genin, D A Piccoli, P S Meltzer, N B Spinner, F S Collins,[...]. Nat Genet 1997
743
4

Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
Agatino Battaglia, H Eugene Hoyme, Bruno Dallapiccola, Elaine Zackai, Louanne Hudgins, Donna McDonald-McGinn, Nadia Bahi-Buisson, Corrado Romano, Charles A Williams, Lisa L Brailey,[...]. Pediatrics 2008
161
4

CFC1 mutations in patients with transposition of the great arteries and double-outlet right ventricle.
Elizabeth Goldmuntz, Richard Bamford, Jayaprakash D Karkera, June dela Cruz, Erich Roessler, Maximilian Muenke. Am J Hum Genet 2002
118
4

Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1.
L Li, I D Krantz, Y Deng, A Genin, A B Banta, C C Collins, M Qi, B J Trask, W L Kuo, J Cochran,[...]. Nat Genet 1997
833
4

Williams-Beuren syndrome.
Barbara R Pober. N Engl J Med 2010
436
4

A restricted spectrum of NRAS mutations causes Noonan syndrome.
Ion C Cirstea, Kerstin Kutsche, Radovan Dvorsky, Lothar Gremer, Claudio Carta, Denise Horn, Amy E Roberts, Francesca Lepri, Torsten Merbitz-Zahradnik, Rainer König,[...]. Nat Genet 2010
194
4


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.