A citation-based method for searching scientific literature

J Burn, P Brennan, J Little, S Holloway, R Coffey, J Somerville, N R Dennis, L Allan, R Arnold, J E Deanfield, M Godman, A Houston, B Keeton, C Oakley, O Scott, E Silove, J Wilkinson, M Pembrey, A S Hunter. Lancet 1998
Times Cited: 222







List of co-cited articles
1166 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Recurrence of congenital heart defects in families.
Nina Øyen, Gry Poulsen, Heather A Boyd, Jan Wohlfahrt, Peter K A Jensen, Mads Melbye. Circulation 2009
182
34

The incidence of congenital heart disease.
Julien I E Hoffman, Samuel Kaplan. J Am Coll Cardiol 2002
33

Genetic basis for congenital heart defects: current knowledge: a scientific statement from the American Heart Association Congenital Cardiac Defects Committee, Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pediatrics.
Mary Ella Pierpont, Craig T Basson, D Woodrow Benson, Bruce D Gelb, Therese M Giglia, Elizabeth Goldmuntz, Glenn McGee, Craig A Sable, Deepak Srivastava, Catherine L Webb. Circulation 2007
527
26


Prospective multicenter study of pregnancy outcomes in women with heart disease.
S C Siu, M Sermer, J M Colman, A N Alvarez, L A Mercier, B C Morton, C M Kells, M L Bergin, M C Kiess, F Marcotte,[...]. Circulation 2001
682
21

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
20

ESC Guidelines on the management of cardiovascular diseases during pregnancy: the Task Force on the Management of Cardiovascular Diseases during Pregnancy of the European Society of Cardiology (ESC).
Vera Regitz-Zagrosek, Carina Blomstrom Lundqvist, Claudio Borghi, Renata Cifkova, Rafael Ferreira, Jean-Michel Foidart, J Simon R Gibbs, Christa Gohlke-Baerwolf, Bulent Gorenek, Bernard Iung,[...]. Eur Heart J 2011
866
19

Congenital heart disease caused by mutations in the transcription factor NKX2-5.
J J Schott, D W Benson, C T Basson, W Pease, G M Silberbach, J P Moak, B J Maron, C E Seidman, J G Seidman. Science 1998
888
18

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
38

Predictors of pregnancy complications in women with congenital heart disease.
Willem Drenthen, Eric Boersma, Ali Balci, Philip Moons, Jolien W Roos-Hesselink, Barbara J M Mulder, Hubert W Vliegen, Arie P J van Dijk, Adriaan A Voors, Sing C Yap,[...]. Eur Heart J 2010
266
18

Outcome of pregnancy in women with congenital heart disease: a literature review.
Willem Drenthen, Petronella G Pieper, Jolien W Roos-Hesselink, Willem A van Lottum, Adriaan A Voors, Barbara J M Mulder, Arie P J van Dijk, Hubert W Vliegen, Sing C Yap, Philip Moons,[...]. J Am Coll Cardiol 2007
307
18

GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5.
Vidu Garg, Irfan S Kathiriya, Robert Barnes, Marie K Schluterman, Isabelle N King, Cheryl A Butler, Caryn R Rothrock, Reenu S Eapen, Kayoko Hirayama-Yamada, Kunitaka Joo,[...]. Nature 2003
797
17

Outcomes of pregnancy in women with tetralogy of Fallot.
Gruschen R Veldtman, Heidi M Connolly, Martha Grogan, Naser M Ammash, Carole A Warnes. J Am Coll Cardiol 2004
112
17

Risks of contraception and pregnancy in heart disease.
Sara Thorne, Anne MacGregor, Catherine Nelson-Piercy. Heart 2006
205
17

Pregnancy outcomes in women with congenital heart disease.
Paul Khairy, David W Ouyang, Susan M Fernandes, Aviva Lee-Parritz, Katherine E Economy, Michael J Landzberg. Circulation 2006
268
16

Hypoplastic left heart syndrome is heritable.
Robert B Hinton, Lisa J Martin, Meredith E Tabangin, Mjaye L Mazwi, Linda H Cripe, D Woodrow Benson. J Am Coll Cardiol 2007
124
16

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
15

Congenital heart disease in the general population: changing prevalence and age distribution.
Ariane J Marelli, Andrew S Mackie, Raluca Ionescu-Ittu, Elham Rahme, Louise Pilote. Circulation 2007
969
15

Recurrence of discordant congenital heart defects in families.
Nina Oyen, Gry Poulsen, Jan Wohlfahrt, Heather A Boyd, Peter K A Jensen, Mads Melbye. Circ Cardiovasc Genet 2010
41
31

Birth prevalence of congenital heart disease worldwide: a systematic review and meta-analysis.
Denise van der Linde, Elisabeth E M Konings, Maarten A Slager, Maarten Witsenburg, Willem A Helbing, Johanna J M Takkenberg, Jolien W Roos-Hesselink. J Am Coll Cardiol 2011
13

Has there been any progress made on pregnancy outcomes among women with pulmonary arterial hypertension?
Elisabeth Bédard, Konstantinos Dimopoulos, Michael A Gatzoulis. Eur Heart J 2009
263
12

Inheritance analysis of congenital left ventricular outflow tract obstruction malformations: Segregation, multiplex relative risk, and heritability.
Kim L McBride, Ricardo Pignatelli, Mark Lewin, Trang Ho, Susan Fernbach, Andres Menesses, Wilbur Lam, Suzanne M Leal, Norman Kaplan, Paul Schliekelman,[...]. Am J Med Genet A 2005
123
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
12

Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease.
Rachel Soemedi, Ian J Wilson, Jamie Bentham, Rebecca Darlay, Ana Töpf, Diana Zelenika, Catherine Cosgrove, Kerry Setchfield, Chris Thornborough, Javier Granados-Riveron,[...]. Am J Hum Genet 2012
180
12




ESC Guidelines for the management of grown-up congenital heart disease (new version 2010).
Helmut Baumgartner, Philipp Bonhoeffer, Natasja M S De Groot, Fokko de Haan, John Erik Deanfield, Nazzareno Galie, Michael A Gatzoulis, Christa Gohlke-Baerwolf, Harald Kaemmerer, Philip Kilner,[...]. Eur Heart J 2010
11


Array comparative genomic hybridization as a diagnostic tool for syndromic heart defects.
Jeroen Breckpot, Bernard Thienpont, Hilde Peeters, Thomy de Ravel, Amihood Singer, Maissa Rayyan, Karel Allegaert, Christine Vanhole, Benedicte Eyskens, Joris Robert Vermeesch,[...]. J Pediatr 2010
59
18

De novo mutations in histone-modifying genes in congenital heart disease.
Samir Zaidi, Murim Choi, Hiroko Wakimoto, Lijiang Ma, Jianming Jiang, John D Overton, Angela Romano-Adesman, Robert D Bjornson, Roger E Breitbart, Kerry K Brown,[...]. Nature 2013
517
11

Pregnancy and delivery in women after Fontan palliation.
W Drenthen, P G Pieper, J W Roos-Hesselink, W A van Lottum, A A Voors, B J M Mulder, A P J van Dijk, H W Vliegen, K M Sollie, P Moons,[...]. Heart 2006
91
10


Congenital cardiovascular malformations: questions on inheritance. Baltimore-Washington Infant Study Group.
C Ferencz, J A Boughman, C A Neill, J I Brenner, L W Perry. J Am Coll Cardiol 1989
89
11

Outcome of pregnancy in patients with structural or ischaemic heart disease: results of a registry of the European Society of Cardiology.
Jolien W Roos-Hesselink, Titia P E Ruys, Jörg I Stein, Ulf Thilén, Gary D Webb, Koichiro Niwa, Harald Kaemmerer, Helmut Baumgartner, Werner Budts, Aldo P Maggioni,[...]. Eur Heart J 2013
210
10

Recurrence of congenital heart disease in cases with familial risk screened prenatally by echocardiography.
Vlasta Fesslova, Jelena Brankovic, Faustina Lalatta, Laura Villa, Valerio Meli, Luciane Piazza, Cristian Ricci. J Pregnancy 2011
25
40

Complete transposition of the great arteries: patterns of congenital heart disease in familial precurrence.
M C Digilio, B Casey, A Toscano, R Calabrò, G Pacileo, M Marasini, E Banaudi, A Giannotti, B Dallapiccola, B Marino. Circulation 2001
61
16

Genetics of congenital heart disease: the glass half empty.
Akl C Fahed, Bruce D Gelb, J G Seidman, Christine E Seidman. Circ Res 2013
304
10

Frequency of 22q11 deletions in patients with conotruncal defects.
E Goldmuntz, B J Clark, L E Mitchell, A F Jawad, B F Cuneo, L Reed, D McDonald-McGinn, P Chien, J Feuer, E H Zackai,[...]. J Am Coll Cardiol 1998
356
9

Heart rate response during exercise and pregnancy outcome in women with congenital heart disease.
George K Lui, Candice K Silversides, Paul Khairy, Sue M Fernandes, Anne Marie Valente, Michelle J Nickolaus, Michael G Earing, Jamil A Aboulhosn, Marlon S Rosenbaum, Stephen Cook,[...]. Circulation 2011
53
16

Coarctation of the aorta: outcome of pregnancy.
L M Beauchesne, H M Connolly, N M Ammash, C A Warnes. J Am Coll Cardiol 2001
139
9

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
9

Microdeletions and microduplications in patients with congenital heart disease and multiple congenital anomalies.
Elizabeth Goldmuntz, Prasuna Paluru, Joseph Glessner, Hakon Hakonarson, Jaclyn A Biegel, Peter S White, Xiaowu Gai, Tamim H Shaikh. Congenit Heart Dis 2011
52
17


Pregnancy in cyanotic congenital heart disease. Outcome of mother and fetus.
P Presbitero, J Somerville, S Stone, E Aruta, D Spiegelhalter, F Rabajoli. Circulation 1994
223
8

Task force 1: the changing profile of congenital heart disease in adult life.
C A Warnes, R Liberthson, G K Danielson, A Dore, L Harris, J I Hoffman, J Somerville, R G Williams, G D Webb. J Am Coll Cardiol 2001
849
8

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
8

Systematic survey of variants in TBX1 in non-syndromic tetralogy of Fallot identifies a novel 57 base pair deletion that reduces transcriptional activity but finds no evidence for association with common variants.
Helen R Griffin, Ana Töpf, Elise Glen, Christiane Zweier, A Graham Stuart, Jonathan Parsons, Ian Peart, John Deanfield, John O'Sullivan, Anita Rauch,[...]. Heart 2010
45
17

NKX2.5 mutations in patients with tetralogy of fallot.
E Goldmuntz, E Geiger, D W Benson. Circulation 2001
228
8

Identification and functional characterization of NODAL rare variants in heterotaxy and isolated cardiovascular malformations.
Bhagyalaxmi Mohapatra, Brett Casey, Hua Li, Trang Ho-Dawson, Liana Smith, Susan D Fernbach, Laura Molinari, Stephen R Niesh, John Lynn Jefferies, William J Craigen,[...]. Hum Mol Genet 2009
91
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.