A citation-based method for searching scientific literature

Xiaoliang Li, Guocheng Shi, Yang Li, Xiaoqing Zhang, Ying Xiang, Teng Wang, Yanxin Li, Huiwen Chen, Qihua Fu, Hong Zhang, Bo Wang. J Med Genet 2020
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


22q11.2 deletion syndrome.
Donna M McDonald-McGinn, Kathleen E Sullivan, Bruno Marino, Nicole Philip, Ann Swillen, Jacob A S Vorstman, Elaine H Zackai, Beverly S Emanuel, Joris R Vermeesch, Bernice E Morrow,[...]. Nat Rev Dis Primers 2015
381
100

Defining the clinical spectrum of deletion 22q11.2.
Nathaniel H Robin, Robert J Shprintzen. J Pediatr 2005
152
100

The recurrent distal 22q11.2 microdeletions are often de novo and do not represent a single clinical entity: a proposed categorization system.
Fady M Mikhail, Rachel D Burnside, Brooke Rush, Jennifer Ibrahim, Robin Godshalk, S Lane Rutledge, Nathaniel H Robin, Maria D Descartes, Andrew J Carroll. Genet Med 2014
27
100

Central 22q11.2 deletions.
Patrick Rump, Nicole de Leeuw, Anthonie J van Essen, Corien C Verschuuren-Bemelmans, Hermine E Veenstra-Knol, Mariëlle E M Swinkels, Wilma Oostdijk, Claudia Ruivenkamp, Willie Reardon, Sonja de Munnik,[...]. Am J Med Genet A 2014
36
100

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
100

DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources.
Helen V Firth, Shola M Richards, A Paul Bevan, Stephen Clayton, Manuel Corpas, Diana Rajan, Steven Van Vooren, Yves Moreau, Roger M Pettett, Nigel P Carter. Am J Hum Genet 2009
920
100


Familial total anomalous pulmonary venous return with 15q11.2 (BP1-BP2) microdeletion.
Yukiko Kuroda, Ikuko Ohashi, Takuya Naruto, Kazumi Ida, Yumi Enomoto, Toshiyuki Saito, Jun-Ichi Nagai, Sadamitsu Yanagi, Hideaki Ueda, Kenji Kurosawa. J Hum Genet 2018
5
100

Phenotypic variability of atypical 22q11.2 deletions not including TBX1.
Judith M A Verhagen, Karin E M Diderich, Grétel Oudesluijs, Grazia M S Mancini, Alex J Eggink, Anna C Verkleij-Hagoort, Irene A L Groenenberg, Patrick J Willems, Frederik A du Plessis, Stella A de Man,[...]. Am J Med Genet A 2012
39
100

Familial total anomalous pulmonary venous return: a large Utah-Idaho family.
S Bleyl, H D Ruttenberg, J C Carey, K Ward. Am J Med Genet 1994
15
100

Another critical region for deletion of 22q11: a study of 100 patients.
H Kurahashi, E Tsuda, R Kohama, T Nakayama, M Masuno, K Imaizumi, T Kamiya, T Sano, S Okada, I Nishisho. Am J Med Genet 1997
57
100

Congenital heart defects in a novel recurrent 22q11.2 deletion harboring the genes CRKL and MAPK1.
Jeroen Breckpot, Bernard Thienpont, Marijke Bauters, Leon-Charles Tranchevent, Marc Gewillig, Karel Allegaert, Joris R Vermeesch, Yves Moreau, Koenraad Devriendt. Am J Med Genet A 2012
30
100

Of mice and men: molecular genetics of congenital heart disease.
Troels Askhøj Andersen, Karin de Linde Lind Troelsen, Lars Allan Larsen. Cell Mol Life Sci 2014
110
100


In the line-up: deleted genes associated with DiGeorge/22q11.2 deletion syndrome: are they all suspects?
Zahra Motahari, Sally Ann Moody, Thomas Michael Maynard, Anthony-Samuel LaMantia. J Neurodev Disord 2019
19
100

Synaptic and Gene Regulatory Mechanisms in Schizophrenia, Autism, and 22q11.2 Copy Number Variant-Mediated Risk for Neuropsychiatric Disorders.
Jennifer K Forsyth, Daniel Nachun, Michael J Gandal, Daniel H Geschwind, Ariana E Anderson, Giovanni Coppola, Carrie E Bearden. Biol Psychiatry 2020
12
100

Duplication and Deletion of 22q11 Associated with Anomalous Pulmonary Venous Connection.
Ruixue Cao, Sijie Liu, Chunjie Liu, Sun Chen, Fen Li, Kun Sun, Rang Xu. Pediatr Cardiol 2018
4
100

Next-generation sequencing identifies novel genes with rare variants in total anomalous pulmonary venous connection.
Xin Shi, Tao Huang, Jing Wang, Yulai Liang, Chang Gu, Yuejuan Xu, Jing Sun, Yanan Lu, Kun Sun, Sun Chen,[...]. EBioMedicine 2018
35
100

Germline recessive mutations in PI4KA are associated with perisylvian polymicrogyria, cerebellar hypoplasia and arthrogryposis.
Alistair T Pagnamenta, Malcolm F Howard, Eva Wisniewski, Niko Popitsch, Samantha J L Knight, David A Keays, Gerardine Quaghebeur, Helen Cox, Phillip Cox, Tamas Balla,[...]. Hum Mol Genet 2015
33
100

The human genome browser at UCSC.
W James Kent, Charles W Sugnet, Terrence S Furey, Krishna M Roskin, Tom H Pringle, Alan M Zahler, David Haussler. Genome Res 2002
100

Mutations in LZTR1 drive human disease by dysregulating RAS ubiquitination.
M Steklov, S Pandolfi, M F Baietti, A Batiuk, P Carai, P Najm, M Zhang, H Jang, F Renzi, Y Cai,[...]. Science 2018
61
100

Chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).
Donna M McDonald-McGinn, Kathleen E Sullivan. Medicine (Baltimore) 2011
227
100

Mouse and human CRKL is dosage sensitive for cardiac outflow tract formation.
Silvia E Racedo, Donna M McDonald-McGinn, Jonathan H Chung, Elizabeth Goldmuntz, Elaine Zackai, Beverly S Emanuel, Bin Zhou, Birgit Funke, Bernice E Morrow. Am J Hum Genet 2015
38
100


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.