A citation-based method for searching scientific literature

Khalid A Fakhro, Murim Choi, Stephanie M Ware, John W Belmont, Jeffrey A Towbin, Richard P Lifton, Mustafa K Khokha, Martina Brueckner. Proc Natl Acad Sci U S A 2011
Times Cited: 158







List of co-cited articles
1273 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
26

The heterotaxy gene GALNT11 glycosylates Notch to orchestrate cilia type and laterality.
Marko T Boskovski, Shiaulou Yuan, Nis Borbye Pedersen, Christoffer Knak Goth, Svetlana Makova, Henrik Clausen, Martina Brueckner, Mustafa K Khokha. Nature 2013
112
25

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
18

Congenital Heart Disease Genetics Uncovers Context-Dependent Organization and Function of Nucleoporins at Cilia.
Florencia Del Viso, Fang Huang, Jordan Myers, Madeleine Chalfant, Yongdeng Zhang, Nooreen Reza, Joerg Bewersdorf, C Patrick Lusk, Mustafa K Khokha. Dev Cell 2016
56
32

Disorders of left-right asymmetry: heterotaxy and situs inversus.
Mardi J Sutherland, Stephanie M Ware. Am J Med Genet C Semin Med Genet 2009
141
17

Two populations of node monocilia initiate left-right asymmetry in the mouse.
James McGrath, Stefan Somlo, Svetlana Makova, Xin Tian, Martina Brueckner. Cell 2003
540
16


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
14

Congenital heart disease and other heterotaxic defects in a large cohort of patients with primary ciliary dyskinesia.
Marcus P Kennedy, Heymut Omran, Margaret W Leigh, Sharon Dell, Lucy Morgan, Paul L Molina, Blair V Robinson, Susan L Minnix, Heike Olbrich, Thomas Severin,[...]. Circulation 2007
245
13

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
182
13

The nodal inhibitor Coco is a critical target of leftward flow in Xenopus.
Axel Schweickert, Philipp Vick, Maike Getwan, Thomas Weber, Isabelle Schneider, Melanie Eberhardt, Tina Beyer, Anke Pachur, Martin Blum. Curr Biol 2010
95
12

CRISPR/Cas9: An inexpensive, efficient loss of function tool to screen human disease genes in Xenopus.
Dipankan Bhattacharya, Chris A Marfo, Davis Li, Maura Lane, Mustafa K Khokha. Dev Biol 2015
80
15

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
12

Rare copy number variants contribute to congenital left-sided heart disease.
Marc-Phillip Hitz, Louis-Philippe Lemieux-Perreault, Christian Marshall, Yassamin Feroz-Zada, Robbie Davies, Shi Wei Yang, Anath Christopher Lionel, Guylaine D'Amours, Emmanuelle Lemyre, Rebecca Cullum,[...]. PLoS Genet 2012
88
12

Novel copy-number variants in a population-based investigation of classic heterotaxy.
Shannon L Rigler, Denise M Kay, Robert J Sicko, Ruzong Fan, Aiyi Liu, Michele Caggana, Marilyn L Browne, Charlotte M Druschel, Paul A Romitti, Lawrence C Brody,[...]. Genet Med 2015
20
55

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
11

Genetics of human heterotaxias.
Lirong Zhu, John W Belmont, Stephanie M Ware. Eur J Hum Genet 2006
84
11

Identification and functional analysis of ZIC3 mutations in heterotaxy and related congenital heart defects.
Stephanie M Ware, Jianlan Peng, Lirong Zhu, Susan Fernbach, Suzanne Colicos, Brett Casey, Jeffrey Towbin, John W Belmont. Am J Hum Genet 2004
171
10

X-linked situs abnormalities result from mutations in ZIC3.
M Gebbia, G B Ferrero, G Pilia, M T Bassi, A Aylsworth, M Penman-Splitt, L M Bird, J S Bamforth, J Burn, D Schlessinger,[...]. Nat Genet 1997
304
10

Xenopus, an ideal model system to study vertebrate left-right asymmetry.
Martin Blum, Tina Beyer, Thomas Weber, Philipp Vick, Philipp Andre, Eva Bitzer, Axel Schweickert. Dev Dyn 2009
71
14

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
10


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
10

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
9

Determination of left-right patterning of the mouse embryo by artificial nodal flow.
Shigenori Nonaka, Hidetaka Shiratori, Yukio Saijoh, Hiroshi Hamada. Nature 2002
429
9

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
9

Control of mucin-type O-glycosylation: a classification of the polypeptide GalNAc-transferase gene family.
Eric P Bennett, Ulla Mandel, Henrik Clausen, Thomas A Gerken, Timothy A Fritz, Lawrence A Tabak. Glycobiology 2012
437
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
92
8

A two-cilia model for vertebrate left-right axis specification.
Clifford J Tabin, Kyle J Vogan. Genes Dev 2003
175
8

The contribution of de novo and rare inherited copy number changes to congenital heart disease in an unselected sample of children with conotruncal defects or hypoplastic left heart disease.
Dorothy Warburton, Michael Ronemus, Jennie Kline, Vaidehi Jobanputra, Ismee Williams, Kwame Anyane-Yeboa, Wendy Chung, Lan Yu, Nancy Wong, Danielle Awad,[...]. Hum Genet 2014
78
10


Rare copy number variations in adults with tetralogy of Fallot implicate novel risk gene pathways.
Candice K Silversides, Anath C Lionel, Gregory Costain, Daniele Merico, Ohsuke Migita, Ben Liu, Tracy Yuen, Jessica Rickaby, Bhooma Thiruvahindrapuram, Christian R Marshall,[...]. PLoS Genet 2012
106
8

The incidence of congenital heart disease.
Julien I E Hoffman, Samuel Kaplan. J Am Coll Cardiol 2002
8

Laterality defects in the national birth defects prevention study (1998-2007): birth prevalence and descriptive epidemiology.
Angela E Lin, Sergey Krikov, Tiffany Riehle-Colarusso, Jaime L Frías, John Belmont, Marlene Anderka, Tal Geva, Kelly D Getz, Lorenzo D Botto. Am J Med Genet A 2014
76
10

Left-right asymmetry in the level of active Nodal protein produced in the node is translated into left-right asymmetry in the lateral plate of mouse embryos.
Aiko Kawasumi, Tetsuya Nakamura, Naomi Iwai, Kenta Yashiro, Yukio Saijoh, Jose Antonio Belo, Hidetaka Shiratori, Hiroshi Hamada. Dev Biol 2011
59
13

Biallelic Mutations in Nuclear Pore Complex Subunit NUP107 Cause Early-Childhood-Onset Steroid-Resistant Nephrotic Syndrome.
Noriko Miyake, Hiroyasu Tsukaguchi, Eriko Koshimizu, Akemi Shono, Satoko Matsunaga, Masaaki Shiina, Yasuhiro Mimura, Shintaro Imamura, Tomonori Hirose, Koji Okudela,[...]. Am J Hum Genet 2015
62
12

RAPGEF5 Regulates Nuclear Translocation of β-Catenin.
John N Griffin, Florencia Del Viso, Anna R Duncan, Andrew Robson, Woong Hwang, Saurabh Kulkarni, Karen J Liu, Mustafa K Khokha. Dev Cell 2018
34
23

Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defects.
R N Bamford, E Roessler, R D Burdine, U Saplakoğlu, J dela Cruz, M Splitt, J A Goodship, J Towbin, P Bowers, G B Ferrero,[...]. Nat Genet 2000
231
7

Cilia-driven leftward flow determines laterality in Xenopus.
Axel Schweickert, Thomas Weber, Tina Beyer, Philipp Vick, Susanne Bogusch, Kerstin Feistel, Martin Blum. Curr Biol 2007
181
7



Mechanism of nodal flow: a conserved symmetry breaking event in left-right axis determination.
Yasushi Okada, Sen Takeda, Yosuke Tanaka, Juan-Carlos Izpisúa Belmonte, Nobutaka Hirokawa. Cell 2005
305
7

A size-exclusion permeability barrier and nucleoporins characterize a ciliary pore complex that regulates transport into cilia.
Hooi Lynn Kee, John F Dishinger, T Lynne Blasius, Chia-Jen Liu, Ben Margolis, Kristen J Verhey. Nat Cell Biol 2012
200
7

Nuclear pore complex composition: a new regulator of tissue-specific and developmental functions.
Marcela Raices, Maximiliano A D'Angelo. Nat Rev Mol Cell Biol 2012
202
7

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
7


Mutation in nuclear pore component NUP155 leads to atrial fibrillation and early sudden cardiac death.
Xianqin Zhang, Shenghan Chen, Shin Yoo, Susmita Chakrabarti, Teng Zhang, Tie Ke, Carlos Oberti, Sandro L Yong, Fang Fang, Lin Li,[...]. Cell 2008
176
7

A change in nuclear pore complex composition regulates cell differentiation.
Maximiliano A D'Angelo, J Sebastian Gomez-Cavazos, Arianna Mei, Daniel H Lackner, Martin W Hetzer. Dev Cell 2012
138
7

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
7

Zic3 is required in the migrating primitive streak for node morphogenesis and left-right patterning.
Mardi J Sutherland, Shuyun Wang, Malgorzata E Quinn, Allison Haaning, Stephanie M Ware. Hum Mol Genet 2013
25
28


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.