A citation-based method for searching scientific literature

Harald Lahm, Meiwen Jia, Martina Dreßen, Felix Wirth, Nazan Puluca, Ralf Gilsbach, Bernard D Keavney, Julie Cleuziou, Nicole Beck, Olga Bondareva, Elda Dzilic, Melchior Burri, Karl C König, Johannes A Ziegelmüller, Claudia Abou-Ajram, Irina Neb, Zhong Zhang, Stefanie A Doppler, Elisa Mastantuono, Peter Lichtner, Gertrud Eckstein, Jürgen Hörer, Peter Ewert, James R Priest, Lutz Hein, Rüdiger Lange, Thomas Meitinger, Heather J Cordell, Bertram Müller-Myhsok, Markus Krane. J Clin Invest 2021
Times Cited: 5







List of co-cited articles
14 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
289
60

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
75
60

Haploinsufficiency of vascular endothelial growth factor related signaling genes is associated with tetralogy of Fallot.
Miriam S Reuter, Rebekah Jobling, Rajiv R Chaturvedi, Roozbeh Manshaei, Gregory Costain, Tracy Heung, Meredith Curtis, S Mohsen Hosseini, Eriskay Liston, Chelsea Lowther,[...]. Genet Med 2019
29
40

Genome-Wide Association Studies and Meta-Analyses for Congenital Heart Defects.
A J Agopian, Elizabeth Goldmuntz, Hakon Hakonarson, Anshuman Sewda, Deanne Taylor, Laura E Mitchell. Circ Cardiovasc Genet 2017
19
40

Recurrence of congenital heart defects in families.
Nina Øyen, Gry Poulsen, Heather A Boyd, Jan Wohlfahrt, Peter K A Jensen, Mads Melbye. Circulation 2009
189
40

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
9
40

A rare missense mutation in MYH6 associates with non-syndromic coarctation of the aorta.
Thorsteinn Bjornsson, Rosa B Thorolfsdottir, Gardar Sveinbjornsson, Patrick Sulem, Gudmundur L Norddahl, Anna Helgadottir, Solveig Gretarsdottir, Audur Magnusdottir, Ragnar Danielsen, Emil L Sigurdsson,[...]. Eur Heart J 2018
23
40

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
349
40

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
166
40

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
529
40

A genome-wide association study identifies two risk loci for congenital heart malformations in Han Chinese populations.
Zhibin Hu, Yongyong Shi, Xuming Mo, Jing Xu, Bijun Zhao, Yuan Lin, Shiwei Yang, Zhengfeng Xu, Juncheng Dai, Shandong Pan,[...]. Nat Genet 2013
50
40

Association analysis identifies new risk loci for congenital heart disease in Chinese populations.
Yuan Lin, Xuejiang Guo, Bijun Zhao, Juanjuan Liu, Min Da, Yang Wen, Yuanli Hu, Bixian Ni, Kai Zhang, Shiwei Yang,[...]. Nat Commun 2015
18
40

Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot.
Heather J Cordell, Ana Töpf, Chrysovalanto Mamasoula, Alex V Postma, Jamie Bentham, Diana Zelenika, Simon Heath, Gillian Blue, Catherine Cosgrove, Javier Granados Riveron,[...]. Hum Mol Genet 2013
58
40

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
40



Genetics and Genomics of Congenital Heart Disease.
Samir Zaidi, Martina Brueckner. Circ Res 2017
155
20

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
20

Large-scale 3D chromatin reconstruction from chromosomal contacts.
Yanlin Zhang, Weiwei Liu, Yu Lin, Yen Kaow Ng, Shuaicheng Li. BMC Genomics 2019
4
25

Genetics of Congenital Heart Disease: Past and Present.
Iolanda Muntean, Rodica Togănel, Theodora Benedek. Biochem Genet 2017
36
20


Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family.
Q Y Li, R A Newbury-Ecob, J A Terrett, D I Wilson, A R Curtis, C H Yi, T Gebuhr, P J Bullen, S C Robson, T Strachan,[...]. Nat Genet 1997
649
20

Genetics and genetic testing in congenital heart disease.
Jason R Cowan, Stephanie M Ware. Clin Perinatol 2015
52
20

Elongated mitochondrial constrictions and fission in muscle fatigue.
Manuela Lavorato, Emanuele Loro, Valentina Debattisti, Tejvir S Khurana, Clara Franzini-Armstrong. J Cell Sci 2018
6
20

Isolation and characterization of the cDNA encoding bovine poly(ADP-ribose) glycohydrolase.
W Lin, J C Amé, N Aboul-Ela, E L Jacobson, M K Jacobson. J Biol Chem 1997
172
20

Expanding functions of ADP-ribosylation in the maintenance of genome integrity.
K Martin-Hernandez, J-M Rodriguez-Vargas, V Schreiber, F Dantzer. Semin Cell Dev Biol 2017
44
20

Measuring the strength of mice.
Robert M J Deacon. J Vis Exp 2013
111
20


A family of macrodomain proteins reverses cellular mono-ADP-ribosylation.
Gytis Jankevicius, Markus Hassler, Barbara Golia, Vladimir Rybin, Martin Zacharias, Gyula Timinszky, Andreas G Ladurner. Nat Struct Mol Biol 2013
203
20

Mini-review: Retarding aging in murine genetic models of neurodegeneration.
Roger L Albin, Richard A Miller. Neurobiol Dis 2016
5
20

mdx(⁵cv) mice manifest more severe muscle dysfunction and diaphragm force deficits than do mdx Mice.
Nicholas Beastrom, Haiyan Lu, Allison Macke, Benjamin D Canan, Eric K Johnson, Christopher M Penton, Brian K Kaspar, Louise R Rodino-Klapac, Lan Zhou, Paul M L Janssen,[...]. Am J Pathol 2011
35
20

Differences among eight inbred strains of mice in motor ability and motor learning on a rotorod.
M P McFadyen, G Kusek, V J Bolivar, L Flaherty. Genes Brain Behav 2003
105
20


Estrogenically regulated LRP16 interacts with estrogen receptor alpha and enhances the receptor's transcriptional activity.
W-D Han, Y-L Zhao, Y-G Meng, L Zang, Z-Q Wu, Q Li, Y-L Si, K Huang, J-M Ba, H Morinaga,[...]. Endocr Relat Cancer 2007
38
20

Comparative analysis of MACROD1, MACROD2 and TARG1 expression, localisation and interactome.
R Žaja, G Aydin, B E Lippok, R Feederle, B Lüscher, K L H Feijs. Sci Rep 2020
9
20


The Conserved Coronavirus Macrodomain Promotes Virulence and Suppresses the Innate Immune Response during Severe Acute Respiratory Syndrome Coronavirus Infection.
Anthony R Fehr, Rudragouda Channappanavar, Gytis Jankevicius, Craig Fett, Jincun Zhao, Jeremiah Athmer, David K Meyerholz, Ivan Ahel, Stanley Perlman. mBio 2016
110
20

The recognition and removal of cellular poly(ADP-ribose) signals.
Eva Barkauskaite, Gytis Jankevicius, Andreas G Ladurner, Ivan Ahel, Gyula Timinszky. FEBS J 2013
86
20

MACROD2 Haploinsufficiency Impairs Catalytic Activity of PARP1 and Promotes Chromosome Instability and Growth of Intestinal Tumors.
Anuratha Sakthianandeswaren, Marie J Parsons, Dmitri Mouradov, Ruth N MacKinnon, Bruno Catimel, Sheng Liu, Michelle Palmieri, Christopher Love, Robert N Jorissen, Shan Li,[...]. Cancer Discov 2018
23
20

ATM induces MacroD2 nuclear export upon DNA damage.
Barbara Golia, Giuliana Katharina Moeller, Gytis Jankevicius, Andreas Schmidt, Anna Hegele, Julia Preißer, Mai Ly Tran, Axel Imhof, Gyula Timinszky. Nucleic Acids Res 2017
15
20

Macrodomain-containing proteins are new mono-ADP-ribosylhydrolases.
Florian Rosenthal, Karla L H Feijs, Emilie Frugier, Mario Bonalli, Alexandra H Forst, Ralph Imhof, Hans C Winkler, David Fischer, Amedeo Caflisch, Paul O Hassa,[...]. Nat Struct Mol Biol 2013
206
20

Energy sensing and regulation of gene expression in skeletal muscle.
Damien Freyssenet. J Appl Physiol (1985) 2007
53
20

Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome.
Shereen G Ghosh, Kerstin Becker, He Huang, Tracy Dixon-Salazar, Guoliang Chai, Vincenzo Salpietro, Lihadh Al-Gazali, Quinten Waisfisz, Haicui Wang, Keith K Vaux,[...]. Am J Hum Genet 2018
25
20

MACROD2 deficiency promotes hepatocellular carcinoma growth and metastasis by activating GSK-3β/β-catenin signaling.
Zheng-Jun Zhou, Chu-Bin Luo, Hao-Yang Xin, Zhi-Qiang Hu, Gui-Qi Zhu, Jia Li, Shao-Lai Zhou. NPJ Genom Med 2020
3
33

Viral macrodomains: a structural and evolutionary assessment of the pharmacological potential.
Johannes Gregor Matthias Rack, Valentina Zorzini, Zihan Zhu, Marion Schuller, Dragana Ahel, Ivan Ahel. Open Biol 2020
18
20

Circadian modulation of the cardiac proteome underpins differential adaptation to morning and evening exercise training: an LC-MS/MS analysis.
Dae Yun Seo, Chang Shin Yoon, Louise Anne Dizon, Sung Ryul Lee, Jae Boum Youm, Won Suk Yang, Hyo-Bum Kwak, Tae Hee Ko, Hyoung Kyu Kim, Jin Han,[...]. Pflugers Arch 2020
4
25

Progress and outlook in studying the substrate specificities of PARPs and related enzymes.
Marcin J Suskiewicz, Luca Palazzo, Rebecca Hughes, Ivan Ahel. FEBS J 2021
13
20

Identification of macrodomain proteins as novel O-acetyl-ADP-ribose deacetylases.
Dawei Chen, Melanie Vollmar, Marianna N Rossi, Claire Phillips, Rolf Kraehenbuehl, Dea Slade, Pawan V Mehrotra, Frank von Delft, Susan K Crosthwaite, Opher Gileadi,[...]. J Biol Chem 2011
111
20

Battery of behavioral tests in mice that models age-associated changes in human motor function.
Jamie N Justice, Christy S Carter, Hannah J Beck, Rachel A Gioscia-Ryan, Matthew McQueen, Roger M Enoka, Douglas R Seals. Age (Dordr) 2014
51
20

ADP-ribosylation: new facets of an ancient modification.
Luca Palazzo, Andreja Mikoč, Ivan Ahel. FEBS J 2017
84
20


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.