A citation-based method for searching scientific literature

Shaobin Lin, Shanshan Shi, Yi Zhou, Yuanjun Ji, Peizhi Huang, Jianzhu Wu, Baojiang Chen, Yanmin Luo. Prenat Diagn 2018
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity



TBX6 null variants and a common hypomorphic allele in congenital scoliosis.
N Wu, X Ming, J Xiao, Z Wu, X Chen, M Shinawi, Y Shen, G Yu, J Liu, H Xie,[...]. N Engl J Med 2015
145
50

Mutations in the pre-replication complex cause Meier-Gorlin syndrome.
Louise S Bicknell, Ernie M H F Bongers, Andrea Leitch, Stephen Brown, Jeroen Schoots, Margaret E Harley, Salim Aftimos, Jumana Y Al-Aama, Michael Bober, Paul A J Brown,[...]. Nat Genet 2011
160
25

A novel approach identifies new differentially methylated regions (DMRs) associated with imprinted genes.
Sanaa Choufani, Jonathan S Shapiro, Martha Susiarjo, Darci T Butcher, Daria Grafodatskaya, Youliang Lou, Jose C Ferreira, Dalila Pinto, Stephen W Scherer, Lisa G Shaffer,[...]. Genome Res 2011
75
25

Discovery of a previously unrecognized microdeletion syndrome of 16p11.2-p12.2.
Blake C Ballif, Sara A Hornor, Elizabeth Jenkins, Suneeta Madan-Khetarpal, Urvashi Surti, Kelly E Jackson, Alexander Asamoah, Pamela L Brock, Gordon C Gowans, Robert L Conway,[...]. Nat Genet 2007
148
25

Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes.
Erin L Heinzen, Rodney A Radtke, Thomas J Urban, Gianpiero L Cavalleri, Chantal Depondt, Anna C Need, Nicole M Walley, Paola Nicoletti, Dongliang Ge, Claudia B Catarino,[...]. Am J Hum Genet 2010
174
25

16p11.2 microdeletion syndrome: a case report.
D Dell'Edera, C Dilucca, A Allegretti, F Simone, M G Lupo, C Liccese, R Davanzo. J Med Case Rep 2018
6
25

Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies.
Heather C Mefford, Hiltrud Muhle, Philipp Ostertag, Sarah von Spiczak, Karen Buysse, Carl Baker, Andre Franke, Alain Malafosse, Pierre Genton, Pierre Thomas,[...]. PLoS Genet 2010
327
25

The association analysis of TBX6 polymorphism with susceptibility to congenital scoliosis in a Chinese Han population.
Qi Fei, Zhihong Wu, Hai Wang, Xi Zhou, Naiguo Wang, Yaozhong Ding, Yipeng Wang, Guixing Qiu. Spine (Phila Pa 1976) 2010
23
25

Chromosomal karyotype in chorionic villi of recurrent spontaneous abortion patients.
Yan Du, Lanting Chen, Jing Lin, Jun Zhu, Na Zhang, Xuemin Qiu, Dajin Li, Ling Wang. Biosci Trends 2018
8
25

The penetrance of copy number variations for schizophrenia and developmental delay.
George Kirov, Elliott Rees, James T R Walters, Valentina Escott-Price, Lyudmila Georgieva, Alexander L Richards, Kimberly D Chambert, Gerwyn Davies, Sophie E Legge, Jennifer L Moran,[...]. Biol Psychiatry 2014
194
25

Methylation screening of reciprocal genome-wide UPDs identifies novel human-specific imprinted genes.
Kazuhiko Nakabayashi, Alex Martin Trujillo, Chiharu Tayama, Cristina Camprubi, Wataru Yoshida, Pablo Lapunzina, Aurora Sanchez, Hidenobu Soejima, Hiroyuki Aburatani, Genta Nagae,[...]. Hum Mol Genet 2011
39
25

Mental retardation and autism associated with recurrent 16p11.2 microdeletion: incomplete penetrance and variable expressivity.
Zivilė Ciuladaitė, Jūratė Kasnauskienė, Loreta Cimbalistienė, Eglė Preikšaitienė, Philippos C Patsalis, Vaidutis Kučinskas. J Appl Genet 2011
11
25

Recurrent 16p11.2 microdeletions in autism.
Ravinesh A Kumar, Samer KaraMohamed, Jyotsna Sudi, Donald F Conrad, Camille Brune, Judith A Badner, T Conrad Gilliam, Norma J Nowak, Edwin H Cook, William B Dobyns,[...]. Hum Mol Genet 2008
461
25

Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation.
Reinhard Ullmann, Gillian Turner, Maria Kirchhoff, Wei Chen, Bruce Tonge, Carla Rosenberg, Michael Field, Angela M Vianna-Morgante, Louise Christie, Ana C Krepischi-Santos,[...]. Hum Mutat 2007
204
25

The sequence and analysis of duplication-rich human chromosome 16.
Joel Martin, Cliff Han, Laurie A Gordon, Astrid Terry, Shyam Prabhakar, Xinwei She, Gary Xie, Uffe Hellsten, Yee Man Chan, Michael Altherr,[...]. Nature 2004
102
25

A genome-wide approach reveals novel imprinted genes expressed in the human placenta.
Sandrine Barbaux, Géraldine Gascoin-Lachambre, Christophe Buffat, Paul Monnier, Françoise Mondon, Marie-Béatrice Tonanny, Amélie Pinard, Jana Auer, Bettina Bessières, Anne Barlier,[...]. Epigenetics 2012
58
25

Prospective chromosome analysis of 3429 amniocentesis samples in China using copy number variation sequencing.
Jing Wang, Lin Chen, Cong Zhou, Li Wang, Hanbing Xie, Yuanyuan Xiao, Hongmei Zhu, Ting Hu, Zhu Zhang, Qian Zhu,[...]. Am J Obstet Gynecol 2018
25
25

Experience of chromosomal microarray applied in prenatal and postnatal settings in Hong Kong.
Shirley S W Cheng, Kelvin Y K Chan, Kelphen K P Leung, Patrick K C Au, Wai-Keung Tam, Samuel K M Li, Ho-Ming Luk, Anita S Y Kan, Brian H Y Chung, Ivan F M Lo,[...]. Am J Med Genet C Semin Med Genet 2019
12
25

Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies.
Carolien G F de Kovel, Holger Trucks, Ingo Helbig, Heather C Mefford, Carl Baker, Costin Leu, Christian Kluck, Hiltrud Muhle, Sarah von Spiczak, Philipp Ostertag,[...]. Brain 2010
311
25

Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant.
F D Hannes, A J Sharp, H C Mefford, T de Ravel, C A Ruivenkamp, M H Breuning, J-P Fryns, K Devriendt, G Van Buggenhout, A Vogels,[...]. J Med Genet 2009
199
25

The essential role of centrosomal NDE1 in human cerebral cortex neurogenesis.
Mehmet Bakircioglu, Ofélia P Carvalho, Maryam Khurshid, James J Cox, Beyhan Tuysuz, Tanyeri Barak, Saliha Yilmaz, Okay Caglayan, Alp Dincer, Adeline K Nicholas,[...]. Am J Hum Genet 2011
106
25


The 15q11.2 BP1-BP2 microdeletion syndrome: a review.
Devin M Cox, Merlin G Butler. Int J Mol Sci 2015
94
25

Phenotypic heterogeneity of genomic disorders and rare copy-number variants.
Santhosh Girirajan, Jill A Rosenfeld, Bradley P Coe, Sumit Parikh, Neil Friedman, Amy Goldstein, Robyn A Filipink, Juliann S McConnell, Brad Angle, Wendy S Meschino,[...]. N Engl J Med 2012
353
25

16p13.11 duplication is a risk factor for a wide spectrum of neuropsychiatric disorders.
Arivudainambi Ramalingam, Xin-Gang Zhou, Stephanie D Fiedler, Sarah J Brawner, Julie M Joyce, Hong-Yu Liu, Shihui Yu. J Hum Genet 2011
70
25

Structural variation of chromosomes in autism spectrum disorder.
Christian R Marshall, Abdul Noor, John B Vincent, Anath C Lionel, Lars Feuk, Jennifer Skaug, Mary Shago, Rainald Moessner, Dalila Pinto, Yan Ren,[...]. Am J Hum Genet 2008
25

Association between microdeletion and microduplication at 16p11.2 and autism.
Lauren A Weiss, Yiping Shen, Joshua M Korn, Dan E Arking, David T Miller, Ragnheidur Fossdal, Evald Saemundsen, Hreinn Stefansson, Manuel A R Ferreira, Todd Green,[...]. N Engl J Med 2008
25

Microdeletion syndrome 16p11.2-p12.2: clinical and molecular characterization.
Maja Hempel, Nuria Rivera Brugués, Janine Wagenstaller, Gaby Lederer, Andrea Weitensteiner, Heide Seidel, Thomas Meitinger, Tim M Strom. Am J Med Genet A 2009
24
25

16p13.11 microduplication in 45 new patients: refined clinical significance and genotype-phenotype correlations.
Laïla Allach El Khattabi, Solveig Heide, Jean-Hubert Caberg, Joris Andrieux, Martine Doco Fenzy, Caroline Vincent-Delorme, Patrick Callier, Sandra Chantot-Bastaraud, Alexandra Afenjar, Odile Boute-Benejean,[...]. J Med Genet 2020
10
25

A familial 593-kb microdeletion of 16p11.2 associated with mental retardation and hemivertebrae.
Keiko Shimojima, Takehiko Inoue, Yuji Fujii, Kousaku Ohno, Toshiyuki Yamamoto. Eur J Med Genet 2009
32
25

Copy number variations of chromosome 16p13.1 region associated with schizophrenia.
A Ingason, D Rujescu, S Cichon, E Sigurdsson, T Sigmundsson, O P H Pietiläinen, J E Buizer-Voskamp, E Strengman, C Francks, P Muglia,[...]. Mol Psychiatry 2011
180
25

A novel microdeletion at 16p11.2 harbors candidate genes for aortic valve development, seizure disorder, and mild mental retardation.
Nader Ghebranious, Philip F Giampietro, Frederic P Wesbrook, Shereif H Rezkalla. Am J Med Genet A 2007
79
25

Divergent origins and concerted expansion of two segmental duplications on chromosome 16.
E E Eichler, M E Johnson, C Alkan, E Tuzun, C Sahinalp, D Misceo, N Archidiacono, M Rocchi. J Hered 2001
20
25

Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals.
E K Bijlsma, A C J Gijsbers, J H M Schuurs-Hoeijmakers, A van Haeringen, D E Fransen van de Putte, B-M Anderlid, J Lundin, P Lapunzina, L A Pérez Jurado, B Delle Chiaie,[...]. Eur J Med Genet 2009
168
25

Congenital disorder of glycosylation type Ik (CDG-Ik): a defect of mannosyltransferase I.
Christian Kranz, Jonas Denecke, Ludwig Lehle, Kristina Sohlbach, Stefanie Jeske, Friedhelm Meinhardt, Rainer Rossi, Sonja Gudowius, Thorsten Marquardt. Am J Hum Genet 2004
55
25

Mutation Update for COL2A1 Gene Variants Associated with Type II Collagenopathies.
Mouna Barat-Houari, Guillaume Sarrabay, Vincent Gatinois, Aurélie Fabre, Bruno Dumont, David Genevieve, Isabelle Touitou. Hum Mutat 2016
61
25


ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data.
Kai Wang, Mingyao Li, Hakon Hakonarson. Nucleic Acids Res 2010
25

Noonan and cardio-facio-cutaneous syndromes: two clinically and genetically overlapping disorders.
A-M Nyström, S Ekvall, E Berglund, M Björkqvist, G Braathen, K Duchen, H Enell, E Holmberg, U Holmlund, M Olsson-Engman,[...]. J Med Genet 2008
58
25


Increased nuchal translucency in fetuses with a normal karyotype-diagnosis and management: An observational study.
Demetra Socolov, Razvan Socolov, Vlad Eusebiu Gorduza, Tudor Butureanu, Ruxandra Stanculescu, Alexandru Carauleanu, Ioana Pavaleanu. Medicine (Baltimore) 2017
9
25

Development of coupling controlled polymerizations by adapter-ligation in mate-pair sequencing for detection of various genomic variants in one single assay.
Zirui Dong, Xia Zhao, Qiaoling Li, Zhenjun Yang, Yang Xi, Andrei Alexeev, Hanjie Shen, Ou Wang, Jie Ruan, Han Ren,[...]. DNA Res 2019
5
25

Quantitative fluorescent polymerase chain reaction for rapid prenatal diagnosis of fetal aneuploidies in chorionic villus sampling in a single institution.
You Jung Shin, Jin Hoon Chung, Do Jin Kim, Hyun Mee Ryu, Moon Young Kim, Jung Yeol Han, June Seek Choi. Obstet Gynecol Sci 2016
4
25

Balanced Chromosomal Rearrangement Detection by Low-Pass Whole-Genome Sequencing.
Zirui Dong, Lingfei Ye, Zhenjun Yang, Haixiao Chen, Jianying Yuan, Huilin Wang, Xiaosen Guo, Yun Li, Jun Wang, Fang Chen,[...]. Curr Protoc Hum Genet 2018
6
25

Improved assay performance of single nucleotide polymorphism array over conventional karyotyping in analyzing products of conception.
Shao-Bin Lin, Ying-Jun Xie, Zheng Chen, Yi Zhou, Jian-Zhu Wu, Zhi-Qiang Zhang, Shan-Shan Shi, Bao-Jiang Chen, Qun Fang. J Chin Med Assoc 2015
17
25

Mapping translocation breakpoints by next-generation sequencing.
Wei Chen, Vera Kalscheuer, Andreas Tzschach, Corinna Menzel, Reinhard Ullmann, Marcel Holger Schulz, Fikret Erdogan, Na Li, Zofia Kijas, Ger Arkesteijn,[...]. Genome Res 2008
98
25

Exome sequencing for prenatal diagnosis of fetuses with sonographic abnormalities.
Suzanne Drury, Hywel Williams, Natalie Trump, Christopher Boustred, Nicholas Lench, Richard H Scott, Lyn S Chitty. Prenat Diagn 2015
108
25

Submicroscopic chromosomal abnormalities in fetuses with increased nuchal translucency and normal karyotype.
Xin Yang, Ru Li, Fang Fu, Yongling Zhang, Dongzhi Li, Can Liao. J Matern Fetal Neonatal Med 2017
15
25

Mechanisms underlying structural variant formation in genomic disorders.
Claudia M B Carvalho, James R Lupski. Nat Rev Genet 2016
268
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.