A citation-based method for searching scientific literature

Joseph T Glessner, Alexander G Bick, Kaoru Ito, Jason Homsy, Laura Rodriguez-Murillo, Menachem Fromer, Erica Mazaika, Badri Vardarajan, Michael Italia, Jeremy Leipzig, Steven R DePalma, Ryan Golhar, Stephan J Sanders, Boris Yamrom, Michael Ronemus, Ivan Iossifov, A Jeremy Willsey, Matthew W State, Jonathan R Kaltman, Peter S White, Yufeng Shen, Dorothy Warburton, Martina Brueckner, Christine Seidman, Elizabeth Goldmuntz, Bruce D Gelb, Richard Lifton, Jonathan Seidman, Hakon Hakonarson, Wendy K Chung. Circ Res 2014
Times Cited: 129



Rachel Soemedi, Ian J Wilson, Jamie Bentham, Rebecca Darlay, Ana Töpf, Diana Zelenika, Catherine Cosgrove, Kerry Setchfield, Chris Thornborough, Javier Granados-Riveron, Gillian M Blue, Jeroen Breckpot, Stephen Hellens, Simon Zwolinkski, Elise Glen, Chrysovalanto Mamasoula, Thahira J Rahman, Darroch Hall, Anita Rauch, Koenraad Devriendt, Marc Gewillig, John O' Sullivan, David S Winlaw, Frances Bu'Lock, J David Brook, Shoumo Bhattacharya, Mark Lathrop, Mauro Santibanez-Koref, Heather J Cordell, Judith A Goodship, Bernard D Keavney. Am J Hum Genet 2012
Times Cited: 182




List of shared articles



Times cited

Congenital heart disease risk loci identified by genome-wide association study in European patients.
Harald Lahm, Meiwen Jia, Martina Dreßen, Felix Wirth, Nazan Puluca, Ralf Gilsbach, Bernard D Keavney, Julie Cleuziou, Nicole Beck, Olga Bondareva,[...]. J Clin Invest 2021
4

Exome Sequencing and Congenital Heart Disease in Sub-Saharan Africa.
Ekanem N Ekure, Adebowale Adeyemo, Hanhan Liu, Ogochukwu Sokunbi, Nnenna Kalu, Ariel F Martinez, Babajide Owosela, Cedrik Tekendo-Ngongang, Yonit A Addissie, Akinsanya Olusegun-Joseph,[...]. Circ Genom Precis Med 2021
0

The ECM as a driver of heart development and repair.
Christopher J Derrick, Emily S Noël. Development 2021
3

CNV Association of Diverse Clinical Phenotypes from eMERGE reveals novel disease biology underlying cardiovascular disease.
Joseph T Glessner, Jin Li, Akshatha Desai, Melody Palmer, Dokyoon Kim, Anastasia Marie Lucas, Xiao Chang, John J Connolly, Berta Almoguera, John B Harley,[...]. Int J Cardiol 2020
3

Genetic Basis of Human Congenital Heart Disease.
Shannon N Nees, Wendy K Chung. Cold Spring Harb Perspect Biol 2020
6

New Insights into the Impact of Genome-Wide Copy Number Variations on Complex Congenital Heart Disease in Saudi Arabia.
Majed J Dasouki, Salma M Wakil, Olfat Al-Harazi, Maarab Alkorashy, Nzioka P Muiya, Editha Andres, Samya Hagos, Haya Aldusery, Nduna Dzimiri, Dilek Colak. OMICS 2020
1

Genetic Contribution to Congenital Heart Disease (CHD).
N A Shabana, Saleem Ullah Shahid, Uzma Irfan. Pediatr Cardiol 2020
7

Association of congenital cardiovascular malformation and neuropsychiatric phenotypes with 15q11.2 (BP1-BP2) deletion in the UK Biobank.
Simon G Williams, Apostol Nakev, Hui Guo, Simon Frain, Gennadiy Tenin, Anna Liakhovitskaia, Priyanka Saha, James R Priest, Kathryn E Hentges, Bernard D Keavney. Eur J Hum Genet 2020
4

Epigenomic and Transcriptomic Dynamics During Human Heart Organogenesis.
Jennifer VanOudenhove, Tara N Yankee, Andrea Wilderman, Justin Cotney. Circ Res 2020
6

De Novo Damaging Variants, Clinical Phenotypes, and Post-Operative Outcomes in Congenital Heart Disease.
Marko T Boskovski, Jason Homsy, Meena Nathan, Lynn A Sleeper, Sarah Morton, Kathryn B Manheimer, Angela Tai, Joshua Gorham, Matthew Lewis, Michael Swartz,[...]. Circ Genom Precis Med 2020
8

Copy number variants detection by microarray and multiplex ligation-dependent probe amplification in congenital heart diseases.
Orsolya Nagy, Katalin Szakszon, Brigitta Orsolya Biró, Gábor Mogyorósy, Dóra Nagy, Bálint Nagy, István Balogh, Anikó Ujfalusi. J Biotechnol 2019
4

Copy number variations in individuals with conotruncal heart defects reveal some shared developmental pathways irrespective of 22q11.2 deletion status.
Hongbo M Xie, Deanne M Taylor, Zhe Zhang, Donna M McDonald-McGinn, Elaine H Zackai, Dwight Stambolian, Hakon Hakonarson, Bernice E Morrow, Beverly S Emanuel, Elizabeth Goldmuntz. Birth Defects Res 2019
1

Estimating the effect size of the 15Q11.2 BP1-BP2 deletion and its contribution to neurodevelopmental symptoms: recommendations for practice.
Aia Elise Jønch, Elise Douard, Clara Moreau, Anke Van Dijck, Marzia Passeggeri, Frank Kooy, Jacques Puechberty, Carolyn Campbell, Damien Sanlaville, Henrietta Lefroy,[...]. J Med Genet 2019
14

Association of Rare Recurrent Copy Number Variants With Congenital Heart Defects Based on Next-Generation Sequencing Data From Family Trios.
Yichuan Liu, Xiao Chang, Joseph Glessner, Huiqi Qu, Lifeng Tian, Dong Li, Kenny Nguyen, Patrick M A Sleiman, Hakon Hakonarson. Front Genet 2019
3

Integration of Large-Scale Genomic Data Sources With Evolutionary History Reveals Novel Genetic Loci for Congenital Heart Disease.
Elisavet Fotiou, Simon Williams, Alexandra Martin-Geary, David L Robertson, Gennadiy Tenin, Kathryn E Hentges, Bernard Keavney. Circ Genom Precis Med 2019
8

Model system identification of novel congenital heart disease gene candidates: focus on RPL13.
Analyne M Schroeder, Massoud Allahyari, Georg Vogler, Maria A Missinato, Tanja Nielsen, Michael S Yu, Jeanne L Theis, Lars A Larsen, Preeya Goyal, Jill A Rosenfeld,[...]. Hum Mol Genet 2019
5

Targeted Next-Generation Sequencing in Patients with Non-syndromic Congenital Heart Disease.
Silvia Pulignani, Cecilia Vecoli, Andrea Borghini, Ilenia Foffa, Lamia Ait-Alì, Maria Grazia Andreassi. Pediatr Cardiol 2018
14

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


Rare variants in SOX17 are associated with pulmonary arterial hypertension with congenital heart disease.
Na Zhu, Carrie L Welch, Jiayao Wang, Philip M Allen, Claudia Gonzaga-Jauregui, Lijiang Ma, Alejandra K King, Usha Krishnan, Erika B Rosenzweig, D Dunbar Ivy,[...]. Genome Med 2018
41

Perspective: DNA Copy Number Variations in Cardiovascular Diseases.
Aatira Vijay, Iti Garg, Mohammad Zahid Ashraf. Epigenet Insights 2018
2

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

Rare copy number variants in patients with congenital conotruncal heart defects.
Hongbo M Xie, Petra Werner, Dwight Stambolian, Joan E Bailey-Wilson, Hakon Hakonarson, Peter S White, Deanne M Taylor, Elizabeth Goldmuntz. Birth Defects Res 2017
12

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

Search for Rare Copy-Number Variants in Congenital Heart Defects Identifies Novel Candidate Genes and a Potential Role for FOXC1 in Patients With Coarctation of the Aorta.
Marta Sanchez-Castro, Hadja Eldjouzi, Eric Charpentier, Pierre-François Busson, Quentin Hauet, Pierre Lindenbaum, Béatrice Delasalle-Guyomarch, Adrien Baudry, Olivier Pichon, Cécile Pascal,[...]. Circ Cardiovasc Genet 2016
19

Genome-wide rare copy number variations contribute to genetic risk for transposition of the great arteries.
Gregory Costain, Anath C Lionel, Lucas Ogura, Christian R Marshall, Stephen W Scherer, Candice K Silversides, Anne S Bassett. Int J Cardiol 2016
15

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

Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome.
Elisabeth E Mlynarski, Michael Xie, Deanne Taylor, Molly B Sheridan, Tingwei Guo, Silvia E Racedo, Donna M McDonald-McGinn, Eva W C Chow, Jacob Vorstman, Ann Swillen,[...]. Hum Genet 2016
25

A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20.
Neil A Hanchard, Shanker Swaminathan, Kristine Bucasas, Dieter Furthner, Susan Fernbach, Mahshid S Azamian, Xueqing Wang, Mark Lewin, Jeffrey A Towbin, Lisa C A D'Alessandro,[...]. Hum Mol Genet 2016
19