A citation-based method for searching scientific literature

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, Joshua M Gorham, Stacey Gabriel, David M Altshuler, Maria de Lourdes Quintanilla-Dieck, Maria Alexandra Artunduaga, Roland D Eavey, Robert M Plenge, Nancy A Shadick, Michael E Weinblatt, Philip L De Jager, David A Hafler, Roger E Breitbart, Jonathan G Seidman, Christine E Seidman. Nat Genet 2009
Times Cited: 296







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



Times Cited
  Times     Co-cited
Similarity


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
8

Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot.
Donna J Page, Matthieu J Miossec, Simon G Williams, Richard M Monaghan, Elisavet Fotiou, Heather J Cordell, Louise Sutcliffe, Ana Topf, Mathieu Bourgey, Guillaume Bourque,[...]. Circ Res 2019
45
17

High incidence of cardiac malformations in connexin40-deficient mice.
Hong Gu, Frank C Smith, Steven M Taffet, Mario Delmar. Circ Res 2003
91
7

Rare variants in NR2F2 cause congenital heart defects in humans.
Saeed Al Turki, Ashok K Manickaraj, Catherine L Mercer, Sebastian S Gerety, Marc-Phillip Hitz, Sarah Lindsay, Lisa C A D'Alessandro, G Jawahar Swaminathan, Jamie Bentham, Anne-Karin Arndt,[...]. Am J Hum Genet 2014
92
7

Regulatory variation in a TBX5 enhancer leads to isolated congenital heart disease.
Scott Smemo, Luciene C Campos, Ivan P Moskowitz, José E Krieger, Alexandre C Pereira, Marcelo A Nobrega. Hum Mol Genet 2012
114
7

Rare copy number variants in isolated sporadic and syndromic atrioventricular septal defects.
James R Priest, Santhosh Girirajan, Tiffany H Vu, Aaron Olson, Evan E Eichler, Michael A Portman. Am J Med Genet A 2012
30
23

The Database of Genomic Variants: a curated collection of structural variation in the human genome.
Jeffrey R MacDonald, Robert Ziman, Ryan K C Yuen, Lars Feuk, Stephen W Scherer. Nucleic Acids Res 2014
632
7

Rare de novo copy number variants in patients with congenital pulmonary atresia.
Li Xie, Jin-Lan Chen, Wei-Zhi Zhang, Shou-Zheng Wang, Tian-Li Zhao, Can Huang, Jian Wang, Jin-Fu Yang, Yi-Feng Yang, Zhi-Ping Tan. PLoS One 2014
15
46

The Congenital Heart Disease Genetic Network Study: rationale, design, and early results.
Bruce Gelb, Martina Brueckner, Wendy Chung, Elizabeth Goldmuntz, Jonathan Kaltman, Juan Pablo Kaski, Richard Kim, Jennie Kline, Laura Mercer-Rosa, George Porter,[...]. Circ Res 2013
88
7


Deletion of ETS-1, a gene in the Jacobsen syndrome critical region, causes ventricular septal defects and abnormal ventricular morphology in mice.
Maoqing Ye, Chris Coldren, Xingqun Liang, Teresa Mattina, Elizabeth Goldmuntz, D Woodrow Benson, Dunbar Ivy, M B Perryman, Lee Ann Garrett-Sinha, Paul Grossfeld. Hum Mol Genet 2010
69
10

The 11q terminal deletion disorder: a prospective study of 110 cases.
Paul D Grossfeld, Teresa Mattina, Zona Lai, Remi Favier, Ken Lyons Jones, Finbarr Cotter, Christopher Jones. Am J Med Genet A 2004
170
7

NKX2.5 mutations in patients with tetralogy of fallot.
E Goldmuntz, E Geiger, D W Benson. Circulation 2001
228
7

Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways.
D W Benson, G M Silberbach, A Kavanaugh-McHugh, C Cottrill, Y Zhang, S Riggs, O Smalls, M C Johnson, M S Watson, J G Seidman,[...]. J Clin Invest 1999
418
7

Burden of potentially pathologic copy number variants is higher in children with isolated congenital heart disease and significantly impairs covariate-adjusted transplant-free survival.
Daniel Seung Kim, Jerry H Kim, Amber A Burt, David R Crosslin, Nancy Burnham, Cecilia E Kim, Donna M McDonald-McGinn, Elaine H Zackai, Susan C Nicolson, Thomas L Spray,[...]. J Thorac Cardiovasc Surg 2016
29
24

Copy-number disorders are a common cause of congenital kidney malformations.
Simone Sanna-Cherchi, Krzysztof Kiryluk, Katelyn E Burgess, Monica Bodria, Matthew G Sampson, Dexter Hadley, Shannon N Nees, Miguel Verbitsky, Brittany J Perry, Roel Sterken,[...]. Am J Hum Genet 2012
122
7

Prenatal diagnosis of congenital heart defect by genome-wide high-resolution SNP array.
Can Liao, Ru Li, Fang Fu, Guie Xie, Yongling Zhang, Min Pan, Jian Li, Dongzhi Li. Prenat Diagn 2014
30
20

Bicuspid aortic valve disease.
Samuel C Siu, Candice K Silversides. J Am Coll Cardiol 2010
477
6

Notch signaling is essential for ventricular chamber development.
Joaquín Grego-Bessa, Luis Luna-Zurita, Gonzalo del Monte, Victoria Bolós, Pedro Melgar, Alejandro Arandilla, Alistair N Garratt, Heesuk Zang, Yoh-Suke Mukouyama, Hanying Chen,[...]. Dev Cell 2007
311
6

NOTCH2 mutations cause Alagille syndrome, a heterogeneous disorder of the notch signaling pathway.
Ryan McDaniell, Daniel M Warthen, Pedro A Sanchez-Lara, Athma Pai, Ian D Krantz, David A Piccoli, Nancy B Spinner. Am J Hum Genet 2006
415
6

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
6

Functionally significant, rare transcription factor variants in tetralogy of Fallot.
Ana Töpf, Helen R Griffin, Elise Glen, Rachel Soemedi, Danielle L Brown, Darroch Hall, Thahira J Rahman, Jyrki J Eloranta, Christoph Jüngst, A Graham Stuart,[...]. PLoS One 2014
38
15

Detection of large-scale variation in the human genome.
A John Iafrate, Lars Feuk, Miguel N Rivera, Marc L Listewnik, Patricia K Donahoe, Ying Qi, Stephen W Scherer, Charles Lee. Nat Genet 2004
6

NKX2.5 mutations in patients with congenital heart disease.
Doff B McElhinney, Elizabeth Geiger, Joshua Blinder, D Woodrow Benson, Elizabeth Goldmuntz. J Am Coll Cardiol 2003
239
6

Analysis of chromosomal structural variation in patients with congenital left-sided cardiac lesions.
Peter S White, Hongbo M Xie, Petra Werner, Joseph Glessner, Brande Latney, Hakon Hakonarson, Elizabeth Goldmuntz. Birth Defects Res A Clin Mol Teratol 2014
11
54

Chromosomal Imbalances in Patients with Congenital Cardiac Defects: A Meta-analysis Reveals Novel Potential Critical Regions Involved in Heart Development.
Thor Thorsson, William W Russell, Nour El-Kashlan, Rachel Soemedi, Jonathan Levine, Sarah B Geisler, Todd Ackley, Aoy Tomita-Mitchell, Jill A Rosenfeld, Ana Töpf,[...]. Congenit Heart Dis 2015
19
31

1q21.1 Microduplication expression in adults.
Alessia Dolcetti, Candice K Silversides, Christian R Marshall, Anath C Lionel, Dimitri J Stavropoulos, Stephen W Scherer, Anne S Bassett. Genet Med 2013
58
10

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data.
Kai Wang, Mingyao Li, Dexter Hadley, Rui Liu, Joseph Glessner, Struan F A Grant, Hakon Hakonarson, Maja Bucan. Genome Res 2007
6

Novel NOTCH1 mutations in patients with bicuspid aortic valve disease and thoracic aortic aneurysms.
Stephen H McKellar, David J Tester, Marineh Yagubyan, Ramanath Majumdar, Michael J Ackerman, Thoralf M Sundt. J Thorac Cardiovasc Surg 2007
178
6

Mutations in NOTCH1 cause Adams-Oliver syndrome.
Anna-Barbara Stittrich, Anna Lehman, Dale L Bodian, Justin Ashworth, Zheyuan Zong, Hong Li, Patricia Lam, Alina Khromykh, Ramaswamy K Iyer, Joseph G Vockley,[...]. Am J Hum Genet 2014
99
6

Jagged1 (JAG1) mutations in patients with tetralogy of Fallot or pulmonic stenosis.
Robert C Bauer, Ayanna O Laney, Rosemarie Smith, Jennifer Gerfen, Jennifer J D Morrissette, Stacy Woyciechowski, Jennifer Garbarini, Kathleen M Loomes, Ian D Krantz, Zsolt Urban,[...]. Hum Mutat 2010
66
9

American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants.
Hutton M Kearney, Erik C Thorland, Kerry K Brown, Fabiola Quintero-Rivera, Sarah T South. Genet Med 2011
513
6

22q11.2 deletion status and disease burden in children and adolescents with tetralogy of Fallot.
Laura Mercer-Rosa, Stephen M Paridon, Mark A Fogel, Jack Rychik, Ronn E Tanel, Huaqing Zhao, Xuemei Zhang, Wei Yang, Justine Shults, Elizabeth Goldmuntz. Circ Cardiovasc Genet 2015
29
20

Noninherited risk factors and congenital cardiovascular defects: current knowledge: a scientific statement from the American Heart Association Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pediatrics.
Kathy J Jenkins, Adolfo Correa, Jeffrey A Feinstein, Lorenzo Botto, Amy E Britt, Stephen R Daniels, Marsha Elixson, Carole A Warnes, Catherine L Webb. Circulation 2007
455
6

Mutations in cardiac T-box factor gene TBX20 are associated with diverse cardiac pathologies, including defects of septation and valvulogenesis and cardiomyopathy.
Edwin P Kirk, Margaret Sunde, Mauro W Costa, Scott A Rankin, Orit Wolstein, M Leticia Castro, Tanya L Butler, Changbaig Hyun, Guanglan Guo, Robyn Otway,[...]. Am J Hum Genet 2007
220
6

Comprehensive genotype-phenotype analysis in 230 patients with tetralogy of Fallot.
Ralf Rauch, Michael Hofbeck, Christiane Zweier, Andreas Koch, Stefan Zink, Udo Trautmann, Juliane Hoyer, Renate Kaulitz, Helmut Singer, Anita Rauch. J Med Genet 2010
86
6

Large recurrent microdeletions associated with schizophrenia.
Hreinn Stefansson, Dan Rujescu, Sven Cichon, Olli P H Pietiläinen, Andres Ingason, Stacy Steinberg, Ragnheidur Fossdal, Engilbert Sigurdsson, Thordur Sigmundsson, Jacobine E Buizer-Voskamp,[...]. Nature 2008
6

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
6

Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice.
E A Lindsay, F Vitelli, H Su, M Morishima, T Huynh, T Pramparo, V Jurecic, G Ogunrinu, H F Sutherland, P J Scambler,[...]. Nature 2001
677
5


Prenatal diagnosis of chromosomal abnormalities in fetuses with abnormal cardiac ultrasound findings: evaluation of chromosomal microarray-based analysis.
I Mademont-Soler, C Morales, A Soler, J M Martínez-Crespo, Y Shen, E Margarit, N Clusellas, M Obón, B L Wu, A Sánchez. Ultrasound Obstet Gynecol 2013
41
12

The changing epidemiology of congenital heart disease.
Teun van der Bom, A Carla Zomer, Aeilko H Zwinderman, Folkert J Meijboom, Berto J Bouma, Barbara J M Mulder. Nat Rev Cardiol 2011
318
5

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
5


Murine Jagged1/Notch signaling in the second heart field orchestrates Fgf8 expression and tissue-tissue interactions during outflow tract development.
Frances A High, Rajan Jain, Jason Z Stoller, Nicole B Antonucci, Min Min Lu, Kathleen M Loomes, Klaus H Kaestner, Warren S Pear, Jonathan A Epstein. J Clin Invest 2009
120
5

Assessment of the role of copy-number variants in 150 patients with congenital heart defects.
Katarzyna Derwińska, Magdalena Bartnik, Barbara Wiśniowiecka-Kowalnik, Mateusz Jagła, Andrzej Rudziński, Jacek J Pietrzyk, Wanda Kawalec, Lidia Ziółkowska, Anna Kutkowska-Kaźmierczak, Tomasz Gambin,[...]. Med Wieku Rozwoj 2012
18
27

Contribution of rare copy number variants to isolated human malformations.
Clara Serra-Juhé, Benjamín Rodríguez-Santiago, Ivon Cuscó, Teresa Vendrell, Núria Camats, Núria Torán, Luis A Pérez-Jurado. PLoS One 2012
17
29

Genetics and genetic testing in congenital heart disease.
Jason R Cowan, Stephanie M Ware. Clin Perinatol 2015
46
10

Congenital heart defects in recurrent reciprocal 1q21.1 deletion and duplication syndromes: rare association with pulmonary valve stenosis.
M Cristina Digilio, Laura Bernardini, Federica Consoli, Francesca R Lepri, M Grazia Giuffrida, Anwar Baban, Cecilia Surace, Rosangela Ferese, Adriano Angioni, Antonio Novelli,[...]. Eur J Med Genet 2013
24
20

Jacobsen syndrome.
Teresa Mattina, Concetta Simona Perrotta, Paul Grossfeld. Orphanet J Rare Dis 2009
103
5


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.