A citation-based method for searching scientific literature

F Erdogan, L A Larsen, L Zhang, Z Tümer, N Tommerup, W Chen, J R Jacobsen, M Schubert, J Jurkatis, A Tzschach, H-H Ropers, R Ullmann. J Med Genet 2008
Times Cited: 91







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



Times Cited
  Times     Co-cited
Similarity



Role of catenins in the development of gap junctions in rat cardiomyocytes.
Jiahn-Chun Wu, Ru-Yin Tsai, Tun-Hui Chung. J Cell Biochem 2003
69
1

A detailed clinical analysis of 13 patients with AUTS2 syndrome further delineates the phenotypic spectrum and underscores the behavioural phenotype.
Gea Beunders, Jiddeke van de Kamp, Pradeep Vasudevan, Jenny Morton, Katrien Smets, Tjitske Kleefstra, Sonja A de Munnik, Janneke Schuurs-Hoeijmakers, Berten Ceulemans, Marcella Zollino,[...]. J Med Genet 2016
24
4

Non-coding genetic variants in human disease.
Feng Zhang, James R Lupski. Hum Mol Genet 2015
213
1

The Human Transcription Factors.
Samuel A Lambert, Arttu Jolma, Laura F Campitelli, Pratyush K Das, Yimeng Yin, Mihai Albu, Xiaoting Chen, Jussi Taipale, Timothy R Hughes, Matthew T Weirauch. Cell 2018
559
1

Looking beyond the genes: the role of non-coding variants in human disease.
Malte Spielmann, Stefan Mundlos. Hum Mol Genet 2016
55
1

TRIM28 regulates sprouting angiogenesis through VEGFR-DLL4-Notch signaling circuit.
Yinfang Wang, Angom Ramcharan Singh, Yuanyuan Zhao, Tao Du, Yitong Huang, Xiaohong Wan, Debabrata Mukhopadhyay, Ying Wang, Nanping Wang, Peng Zhang. FASEB J 2020
4
25

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
6
16

The prevalence of genetic diagnoses in fetuses with severe congenital heart defects.
Amber E L van Nisselrooij, Malou A Lugthart, Sally-Ann Clur, Ingeborg H Linskens, Eva Pajkrt, Lukas A Rammeloo, Lieke Rozendaal, Nico A Blom, Jan M M van Lith, Alida C Knegt,[...]. Genet Med 2020
15
6

Three year experience of a clinical cardiovascular genetics program for infants with congenital heart disease.
Gabrielle C Geddes, Erin Syverson, Michael G Earing. Congenit Heart Dis 2019
5
20

Chromosomal microarray analysis in fetuses with an isolated congenital heart defect: A retrospective, nationwide, multicenter study in France.
Marguerite Hureaux, Sarah Guterman, Bérénice Hervé, Marianne Till, Sylvie Jaillard, Sylvie Redon, Myléne Valduga, Charles Coutton, Chantal Missirian, Fabienne Prieur,[...]. Prenat Diagn 2019
5
20

The Cardiac Genome Clinic: implementing genome sequencing in pediatric heart disease.
Miriam S Reuter, Rajiv R Chaturvedi, Eriskay Liston, Roozbeh Manshaei, Ritu B Aul, Sarah Bowdin, Iris Cohn, Meredith Curtis, Priya Dhir, Robin Z Hayeems,[...]. Genet Med 2020
11
9

Chromosomal microarray analysis in the investigation of prenatally diagnosed congenital heart disease.
Hiba J Mustafa, Katherine M Jacobs, Katelyn M Tessier, Shanti L Narasimhan, Alena N Tofte, Allison R McCarter, Sarah N Cross. Am J Obstet Gynecol MFM 2020
1
100

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
21
4

Evaluation and diagnosis of the dysmorphic infant.
Kelly L Jones, Margaret P Adam. Clin Perinatol 2015
8
12

Increasing the diagnostic yield of exome sequencing by copy number variant analysis.
Daniel S Marchuk, Kristy Crooks, Natasha Strande, Kathleen Kaiser-Rogers, Laura V Milko, Alicia Brandt, Alexandra Arreola, Christian R Tilley, Chris Bizon, Neeta L Vora,[...]. PLoS One 2018
26
3

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
1

A Comprehensive Clinical Genetics Approach to Critical Congenital Heart Disease in Infancy.
Amy R Shikany, Benjamin J Landis, Ashley Parrott, Erin M Miller, Alyxis Coyan, Lauren Walters, Robert B Hinton, Paula Goldenberg, Stephanie M Ware. J Pediatr 2020
3
33

Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition.
Dennis van der Meer, Ida E Sønderby, Tobias Kaufmann, G Bragi Walters, Abdel Abdellaoui, David Ames, Katrin Amunts, Micael Andersson, Nicola J Armstrong, Manon Bernard,[...]. JAMA Psychiatry 2020
22
4

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
20
5

Exome sequencing compared with standard genetic tests for critically ill infants with suspected genetic conditions.
Hadley Stevens Smith, John M Swint, Seema R Lalani, Marcia C de Oliveira Otto, Jose-Miguel Yamal, Heidi V Russell, Brendan H Lee. Genet Med 2020
4
25

Family-based whole-genome sequencing identifies compound heterozygous protein-coding and noncoding mutations in tetralogy of Fallot.
Yifeng Wang, Tao Jiang, Pushi Tang, Yifei Wu, Zhu Jiang, Juncheng Dai, Yayun Gu, Jing Xu, Min Da, Hongxia Ma,[...]. Gene 2020
2
50

Current Practice and Utility of Chromosome Microarray Analysis in Infants Undergoing Cardiac Surgery.
Jason R Buckley, Minoo N Kavarana, Shahryar M Chowdhury, Mark A Scheurer. Congenit Heart Dis 2015
10
10


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.