A citation-based method for searching scientific literature

Johanna Winberg, Håkan Berggren, Torsten Malm, Sune Johansson, Jens Johansson Ramgren, Boris Nilsson, Agne Liedén, Agneta Nordenskjöld, Peter Gustavsson, Ann Nordgren. Eur J Med Genet 2015
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data.
Joseph T Glessner, Alexander G Bick, Kaoru Ito, Jason Homsy, Laura Rodriguez-Murillo, Menachem Fromer, Erica Mazaika, Badri Vardarajan, Michael Italia, Jeremy Leipzig,[...]. Circ Res 2014
129
50

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
50

The contribution of de novo coding mutations to autism spectrum disorder.
Ivan Iossifov, Brian J O'Roak, Stephan J Sanders, Michael Ronemus, Niklas Krumm, Dan Levy, Holly A Stessman, Kali T Witherspoon, Laura Vives, Karynne E Patterson,[...]. Nature 2014
50

A genomic view of mosaicism and human disease.
Leslie G Biesecker, Nancy B Spinner. Nat Rev Genet 2013
324
50

Somatic mosaicism for copy number variation in differentiated human tissues.
Arkadiusz Piotrowski, Carl E G Bruder, Robin Andersson, Teresita Diaz de Ståhl, Uwe Menzel, Johanna Sandgren, Andrzej Poplawski, Desiree von Tell, Chiquito Crasto, Adam Bogdan,[...]. Hum Mutat 2008
151
50

Genome-wide mapping of copy number variations in patients with both anorectal malformations and central nervous system abnormalities.
Gabriel C Dworschak, Markus Draaken, Alina C Hilger, Charlotte Schramm, Enrika Bartels, Eberhard Schmiedeke, Sabine Grasshoff-Derr, Stefanie Märzheuser, Stefan Holland-Cunz, Martin Lacher,[...]. Birth Defects Res A Clin Mol Teratol 2015
13
50

Rare copy number variants contribute pathogenic alleles in patients with intestinal malrotation.
Karin Salehi Karlslätt, Maria Pettersson, Nina Jäntti, Przemyslaw Szafranski, Tomas Wester, Britt Husberg, Ulla Ullberg, Pawel Stankiewicz, Ann Nordgren, Johanna Lundin,[...]. Mol Genet Genomic Med 2019
6
50

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
516
50

Mutation screening and array comparative genomic hybridization using a 180K oligonucleotide array in VACTERL association.
Johanna Winberg, Peter Gustavsson, Nikos Papadogiannakis, Ellika Sahlin, Frideborg Bradley, Edvard Nordenskjöld, Pär-Johan Svensson, Göran Annerén, Erik Iwarsson, Ann Nordgren,[...]. PLoS One 2014
20
50

MTHFR C677T polymorphism and risk of congenital heart defects: evidence from 29 case-control and TDT studies.
Wei Wang, Yujia Wang, Fangqi Gong, Weihua Zhu, Songling Fu. PLoS One 2013
35
25

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
25

Consanguinity and complex cardiac anomalies with situs ambiguus.
A R Gatrad, A P Read, G H Watson. Arch Dis Child 1984
50
25

Predictors of developmental disabilities after open heart surgery in young children with congenital heart defects.
Catherine Limperopoulos, Annette Majnemer, Michael I Shevell, Charles Rohlicek, Bernard Rosenblatt, Christo Tchervenkov, H Z Darwish. J Pediatr 2002
192
25

Utility of genetic evaluation in infants with congenital heart defects admitted to the cardiac intensive care unit.
Rebecca C Ahrens-Nicklas, Shama Khan, Jennifer Garbarini, Stacy Woyciechowski, Lisa D'Alessandro, Elaine H Zackai, Matthew A Deardorff, Elizabeth Goldmuntz. Am J Med Genet A 2016
15
25



Transcriptional Impact of Rare and Private Copy Number Variants in Hypoplastic Left Heart Syndrome.
Steven C Glidewell, Shelley D Miyamoto, Paul D Grossfeld, David E Clouthier, Christopher D Coldren, Robert S Stearman, Mark W Geraci. Clin Transl Sci 2015
11
25

Dynamic and coordinated epigenetic regulation of developmental transitions in the cardiac lineage.
Joseph A Wamstad, Jeffrey M Alexander, Rebecca M Truty, Avanti Shrikumar, Fugen Li, Kirsten E Eilertson, Huiming Ding, John N Wylie, Alexander R Pico, John A Capra,[...]. Cell 2012
411
25

Brain in Congenital Heart Disease Across the Lifespan: The Cumulative Burden of Injury.
Ariane Marelli, Steven P Miller, Bradley Scott Marino, Angela L Jefferson, Jane W Newburger. Circulation 2016
131
25

Birth prevalence of congenital heart defects in Norway 1994-2009--a nationwide study.
Elisabeth Leirgul, Tatiana Fomina, Kristoffer Brodwall, Gottfried Greve, Henrik Holmstrøm, Stein Emil Vollset, Grethe S Tell, Nina Øyen. Am Heart J 2014
60
25

Genetics of bicuspid aortic valve aortopathy.
Maria G Andreassi, Alessandro Della Corte. Curr Opin Cardiol 2016
37
25

Over-expression of DSCAM and COL6A2 cooperatively generates congenital heart defects.
Tamar R Grossman, Amir Gamliel, Robert J Wessells, Ouarda Taghli-Lamallem, Kristen Jepsen, Karen Ocorr, Julie R Korenberg, Kirk L Peterson, Michael G Rosenfeld, Rolf Bodmer,[...]. PLoS Genet 2011
47
25

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
25

De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart Defects.
James R Priest, Kazutoyo Osoegawa, Nebil Mohammed, Vivek Nanda, Ramendra Kundu, Kathleen Schultz, Edward J Lammer, Santhosh Girirajan, Todd Scheetz, Daryl Waggott,[...]. PLoS Genet 2016
59
25

Abnormal brain development in newborns with congenital heart disease.
Steven P Miller, Patrick S McQuillen, Shannon Hamrick, Duan Xu, David V Glidden, Natalie Charlton, Tom Karl, Anthony Azakie, Donna M Ferriero, A James Barkovich,[...]. N Engl J Med 2007
464
25

Consanguinity and the risk of congenital heart disease.
Joseph T C Shieh, Alan H Bittles, Louanne Hudgins. Am J Med Genet A 2012
40
25

Genetic diagnosis by whole exome capture and massively parallel DNA sequencing.
Murim Choi, Ute I Scholl, Weizhen Ji, Tiewen Liu, Irina R Tikhonova, Paul Zumbo, Ahmet Nayir, Ayşin Bakkaloğlu, Seza Ozen, Sami Sanjad,[...]. Proc Natl Acad Sci U S A 2009
836
25

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
25




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
297
25

An excess of deleterious variants in VEGF-A pathway genes in Down-syndrome-associated atrioventricular septal defects.
Christine Ackerman, Adam E Locke, Eleanor Feingold, Benjamin Reshey, Karina Espana, Janita Thusberg, Sean Mooney, Lora J H Bean, Kenneth J Dooley, Clifford L Cua,[...]. Am J Hum Genet 2012
66
25

Endothelial cilia mediate low flow sensing during zebrafish vascular development.
Jacky G Goetz, Emily Steed, Rita R Ferreira, Stéphane Roth, Caroline Ramspacher, Francesco Boselli, Gilles Charvin, Michael Liebling, Claire Wyart, Yannick Schwab,[...]. Cell Rep 2014
125
25

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
25

The diagnostic value of next generation sequencing in familial nonsyndromic congenital heart defects.
Yaojuan Jia, Jacoba J Louw, Jeroen Breckpot, Bert Callewaert, Catherine Barrea, Yves Sznajer, Marc Gewillig, Erika Souche, Luc Dehaspe, Joris Robert Vermeesch,[...]. Am J Med Genet A 2015
31
25

Influence of genetic and maternal diabetes in the pathogenesis of visceroatrial heterotaxy in mice.
M Morishima, H Yasui, M Ando, M Nakazawa, A Takao. Teratology 1996
27
25

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
25

Targeted capture and massively parallel sequencing of 12 human exomes.
Sarah B Ng, Emily H Turner, Peggy D Robertson, Steven D Flygare, Abigail W Bigham, Choli Lee, Tristan Shaffer, Michelle Wong, Arindam Bhattacharjee, Evan E Eichler,[...]. Nature 2009
25

SHROOM3 is a novel candidate for heterotaxy identified by whole exome sequencing.
Muhammad Tariq, John W Belmont, Seema Lalani, Teresa Smolarek, Stephanie M Ware. Genome Biol 2011
42
25

A human laterality disorder caused by a homozygous deleterious mutation in MMP21.
Zeev Perles, Sungjin Moon, Asaf Ta-Shma, Barak Yaacov, Ludmila Francescatto, Simon Edvardson, Azaria J J T Rein, Orly Elpeleg, Nicholas Katsanis. J Med Genet 2015
27
25

Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome.
C T Basson, D R Bachinsky, R C Lin, T Levi, J A Elkins, J Soults, D Grayzel, E Kroumpouzou, T A Traill, J Leblanc-Straceski,[...]. Nat Genet 1997
770
25

Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry.
Heike Olbrich, Karsten Häffner, Andreas Kispert, Alexander Völkel, Andreas Volz, Gürsel Sasmaz, Richard Reinhardt, Steffen Hennig, Hans Lehrach, Nikolaus Konietzko,[...]. Nat Genet 2002
349
25


Mosaic type-1 NF1 microdeletions as a cause of both generalized and segmental neurofibromatosis type-1 (NF1).
Ludwine Messiaen, Julia Vogt, Kathrin Bengesser, Chuanhua Fu, Fady Mikhail, Eduard Serra, Carles Garcia-Linares, David N Cooper, Conxi Lazaro, Hildegard Kehrer-Sawatzki. Hum Mutat 2011
78
25

Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.
Heather J Cordell, Jamie Bentham, Ana Topf, Diana Zelenika, Simon Heath, Chrysovalanto Mamasoula, Catherine Cosgrove, Gillian Blue, Javier Granados-Riveron, Kerry Setchfield,[...]. Nat Genet 2013
74
25


Cilia at the node of mouse embryos sense fluid flow for left-right determination via Pkd2.
Satoko Yoshiba, Hidetaka Shiratori, Ivana Y Kuo, Aiko Kawasumi, Kyosuke Shinohara, Shigenori Nonaka, Yasuko Asai, Genta Sasaki, Jose Antonio Belo, Hiroshi Sasaki,[...]. Science 2012
183
25

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
25

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
746
25


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.