A citation-based method for searching scientific literature

Mary Ella Pierpont, Martina Brueckner, Wendy K Chung, Vidu Garg, Ronald V Lacro, Amy L McGuire, Seema Mital, James R Priest, William T Pu, Amy Roberts, Stephanie M Ware, Bruce D Gelb, Mark W Russell. Circulation 2018
Times Cited: 111







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



Times Cited
  Times     Co-cited
Similarity


Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands.
Sheng Chih Jin, Jason Homsy, Samir Zaidi, Qiongshi Lu, Sarah Morton, Steven R DePalma, Xue Zeng, Hongjian Qi, Weni Chang, Michael C Sierant,[...]. Nat Genet 2017
271
32

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
523
24

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
342
23

Genetics and Genomics of Congenital Heart Disease.
Samir Zaidi, Martina Brueckner. Circ Res 2017
150
20

The incidence of congenital heart disease.
Julien I E Hoffman, Samuel Kaplan. J Am Coll Cardiol 2002
20

Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing.
Alejandro Sifrim, Marc-Phillip Hitz, Anna Wilsdon, Jeroen Breckpot, Saeed H Al Turki, Bernard Thienpont, Jeremy McRae, Tomas W Fitzgerald, Tarjinder Singh, Ganesh Jawahar Swaminathan,[...]. Nat Genet 2016
160
19

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
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
16

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
14

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
798
13

Genetics and genetic testing in congenital heart disease.
Jason R Cowan, Stephanie M Ware. Clin Perinatol 2015
48
27

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
47
25

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
530
12

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
891
11

Mutations in NOTCH1 cause aortic valve disease.
Vidu Garg, Alecia N Muth, Joshua F Ransom, Marie K Schluterman, Robert Barnes, Isabelle N King, Paul D Grossfeld, Deepak Srivastava. Nature 2005
903
11

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
90
12

Lifetime prevalence of congenital heart disease in the general population from 2000 to 2010.
Ariane J Marelli, Raluca Ionescu-Ittu, Andrew S Mackie, Liming Guo, Nandini Dendukuri, Mohammed Kaouache. Circulation 2014
511
11

Recurrence of congenital heart defects in families.
Nina Øyen, Gry Poulsen, Heather A Boyd, Jan Wohlfahrt, Peter K A Jensen, Mads Melbye. Circulation 2009
185
10

The complex genetics of hypoplastic left heart syndrome.
Xiaoqin Liu, Hisato Yagi, Shazina Saeed, Abha S Bais, George C Gabriel, Zhaohan Chen, Kevin A Peterson, You Li, Molly C Schwartz, William T Reynolds,[...]. Nat Genet 2017
77
12

Global birth prevalence of congenital heart defects 1970-2017: updated systematic review and meta-analysis of 260 studies.
Yingjuan Liu, Sen Chen, Liesl Zühlke, Graeme C Black, Mun-Kit Choy, Ningxiu Li, Bernard D Keavney. Int J Epidemiol 2019
133
9

The contribution of chromosomal abnormalities to congenital heart defects: a population-based study.
Robert J Hartman, Sonja A Rasmussen, Lorenzo D Botto, Tiffany Riehle-Colarusso, Christa L Martin, Janet D Cragan, Mikyong Shin, Adolfo Correa. Pediatr Cardiol 2011
102
8

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
8

Advances in the Genetics of Congenital Heart Disease: A Clinician's Guide.
Gillian M Blue, Edwin P Kirk, Eleni Giannoulatou, Gary F Sholler, Sally L Dunwoodie, Richard P Harvey, David S Winlaw. J Am Coll Cardiol 2017
56
14

A general framework for estimating the relative pathogenicity of human genetic variants.
Martin Kircher, Daniela M Witten, Preti Jain, Brian J O'Roak, Gregory M Cooper, Jay Shendure. Nat Genet 2014
8

Genomic analyses implicate noncoding de novo variants in congenital heart disease.
Felix Richter, Sarah U Morton, Seong Won Kim, Alexander Kitaygorodsky, Lauren K Wasson, Kathleen M Chen, Jian Zhou, Hongjian Qi, Nihir Patel, Steven R DePalma,[...]. Nat Genet 2020
22
36

Single-cell analysis of cardiogenesis reveals basis for organ-level developmental defects.
T Yvanka de Soysa, Sanjeev S Ranade, Satoshi Okawa, Srikanth Ravichandran, Yu Huang, Hazel T Salunga, Amelia Schricker, Antonio Del Sol, Casey A Gifford, Deepak Srivastava. Nature 2019
59
13

Recessive MYH6 Mutations in Hypoplastic Left Heart With Reduced Ejection Fraction.
Jeanne L Theis, Michael T Zimmermann, Jared M Evans, Bruce W Eckloff, Eric D Wieben, Muhammad Y Qureshi, Patrick W O'Leary, Timothy M Olson. Circ Cardiovasc Genet 2015
39
17

Seeking causes: Classifying and evaluating congenital heart defects in etiologic studies.
Lorenzo D Botto, Angela E Lin, Tiffany Riehle-Colarusso, Sadia Malik, Adolfo Correa. Birth Defects Res A Clin Mol Teratol 2007
271
7

Cardiovascular malformations caused by NOTCH1 mutations do not keep left: data on 428 probands with left-sided CHD and their families.
Wilhelmina S Kerstjens-Frederikse, Ingrid M B H van de Laar, Yvonne J Vos, Judith M A Verhagen, Rolf M F Berger, Klaske D Lichtenbelt, Jolien S Klein Wassink-Ruiter, Paul A van der Zwaag, Gideon J du Marchie Sarvaas, Klasien A Bergman,[...]. Genet Med 2016
59
11

Advances in the Understanding of the Genetic Determinants of Congenital Heart Disease and Their Impact on Clinical Outcomes.
Mark W Russell, Wendy K Chung, Jonathan R Kaltman, Thomas A Miller. J Am Heart Assoc 2018
36
19

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
458
7

Prevalence of congenital heart defects in metropolitan Atlanta, 1998-2005.
Mark D Reller, Matthew J Strickland, Tiffany Riehle-Colarusso, William T Mahle, Adolfo Correa. J Pediatr 2008
546
7

The deployment of cell lineages that form the mammalian heart.
Sigolène M Meilhac, Margaret E Buckingham. Nat Rev Cardiol 2018
68
8

Family Based Whole Exome Sequencing Reveals the Multifaceted Role of Notch Signaling in Congenital Heart Disease.
Christoph Preuss, Melanie Capredon, Florian Wünnemann, Philippe Chetaille, Andrea Prince, Beatrice Godard, Severine Leclerc, Nara Sobreira, Hua Ling, Philip Awadalla,[...]. PLoS Genet 2016
32
18

Genetic evaluation of patients with congenital heart disease.
Gabrielle C Geddes, Michael G Earing. Curr Opin Pediatr 2018
10
60

Genetic Testing Protocol Reduces Costs and Increases Rate of Genetic Diagnosis in Infants with Congenital Heart Disease.
Gabrielle C Geddes, Donald Basel, Peter Frommelt, Aaron Kinney, Michael Earing. Pediatr Cardiol 2017
15
40

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
93
6

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
54
11

Global genetic analysis in mice unveils central role for cilia in congenital heart disease.
You Li, Nikolai T Klena, George C Gabriel, Xiaoqin Liu, Andrew J Kim, Kristi Lemke, Yu Chen, Bishwanath Chatterjee, William Devine, Rama Rao Damerla,[...]. Nature 2015
221
6

Submicroscopic chromosomal imbalances detected by array-CGH are a frequent cause of congenital heart defects in selected patients.
Bernard Thienpont, Luc Mertens, Thomy de Ravel, Benedicte Eyskens, Derize Boshoff, Nicole Maas, Jean-Pierre Fryns, Marc Gewillig, Joris R Vermeesch, Koen Devriendt. Eur Heart J 2007
134
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
679
6

The Congenital Heart Disease Genetic Network Study: Cohort description.
Thanh T Hoang, Elizabeth Goldmuntz, Amy E Roberts, Wendy K Chung, Jennie K Kline, John E Deanfield, Alessandro Giardini, Adolfo Aleman, Bruce D Gelb, Meghan Mac Neal,[...]. PLoS One 2018
34
17

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

Neurodevelopmental outcomes in children with congenital heart disease: evaluation and management: a scientific statement from the American Heart Association.
Bradley S Marino, Paul H Lipkin, Jane W Newburger, Georgina Peacock, Marsha Gerdes, J William Gaynor, Kathleen A Mussatto, Karen Uzark, Caren S Goldberg, Walter H Johnson,[...]. Circulation 2012
658
6


Identification of clinically actionable variants from genome sequencing of families with congenital heart disease.
Dimuthu Alankarage, Eddie Ip, Justin O Szot, Jacob Munro, Gillian M Blue, Katrina Harrison, Hartmut Cuny, Annabelle Enriquez, Michael Troup, David T Humphreys,[...]. Genet Med 2019
19
31

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
321
6

A Screening Approach to Identify Clinically Actionable Variants Causing Congenital Heart Disease in Exome Data.
Justin O Szot, Hartmut Cuny, Gillian M Blue, David T Humphreys, Eddie Ip, Katrina Harrison, Gary F Sholler, Eleni Giannoulatou, Paul Leo, Emma L Duncan,[...]. Circ Genom Precis Med 2018
33
15

Notch and interacting signalling pathways in cardiac development, disease, and regeneration.
Donal MacGrogan, Juliane Münch, José Luis de la Pompa. Nat Rev Cardiol 2018
59
8

Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease.
Stephanie LaHaye, Don Corsmeier, Madhumita Basu, Jessica L Bowman, Sara Fitzgerald-Butt, Gloria Zender, Kevin Bosse, Kim L McBride, Peter White, Vidu Garg. Circ Cardiovasc Genet 2016
37
13


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.