A citation-based method for searching scientific literature

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, Marie Pierre Cordier, Laurence Faivre, Christine Francannet, Marion Gerard, Alice Goldenberg, Alice Masurel-Paulet, Anne-Laure Mosca-Boidron, Nathalie Marle, Anne Moncla, Nathalie Le Meur, Michèle Mathieu-Dramard, Ghislaine Plessis, Gaetan Lesca, Massimiliano Rossi, Patrick Edery, Andrée Delahaye-Duriez, Loïc De Pontual, Anne Claude Tabet, Aziza Lebbar, Lesley Suiro, Christine Ioos, Abdelhafid Natiq, Siham Chafai Elalaoui, Chantal Missirian, Aline Receveur, Caroline François-Fiquet, Pascal Garnier, Catherine Yardin, Cécile Laroche, Philippe Vago, Damien Sanlaville, Jean Michel Dupont, Brigitte Benzacken, Eva Pipiras. J Med Genet 2020
Times Cited: 10







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



Times Cited
  Times     Co-cited
Similarity


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
50

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
50

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
30

Phenotypic manifestations of copy number variation in chromosome 16p13.11.
Sandesh C Sreenath Nagamani, Ayelet Erez, Patricia Bader, Seema R Lalani, Daryl A Scott, Fernando Scaglia, Sharon E Plon, Chun-Hui Tsai, Tyler Reimschisel, Elizabeth Roeder,[...]. Eur J Hum Genet 2011
69
30

Chromosomal microarray versus karyotyping for prenatal diagnosis.
Ronald J Wapner, Christa Lese Martin, Brynn Levy, Blake C Ballif, Christine M Eng, Julia M Zachary, Melissa Savage, Lawrence D Platt, Daniel Saltzman, William A Grobman,[...]. N Engl J Med 2012
643
30

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
33

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
20

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
20


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
20

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
20

Common genetic variants on 5p14.1 associate with autism spectrum disorders.
Kai Wang, Haitao Zhang, Deqiong Ma, Maja Bucan, Joseph T Glessner, Brett S Abrahams, Daria Salyakina, Marcin Imielinski, Jonathan P Bradfield, Patrick M A Sleiman,[...]. Nature 2009
662
20

Clinical utility gene card for: 16p13.11 microdeletion syndrome.
Maria Tropeano, Joris Andrieux, David A Collier. Eur J Hum Genet 2014
9
22

Recurrent chromosome 16p13.1 duplications are a risk factor for aortic dissections.
Shao-Qing Kuang, Dong-Chuan Guo, Siddharth K Prakash, Merry-Lynn N McDonald, Ralph J Johnson, Min Wang, Ellen S Regalado, Ludivine Russell, Jiu-Mei Cao, Callie Kwartler,[...]. PLoS Genet 2011
58
20

Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen).
Erin Rooney Riggs, Erica F Andersen, Athena M Cherry, Sibel Kantarci, Hutton Kearney, Ankita Patel, Gordana Raca, Deborah I Ritter, Sarah T South, Erik C Thorland,[...]. Genet Med 2020
136
20

A method for rapid, targeted CNV genotyping identifies rare variants associated with neurocognitive disease.
Heather C Mefford, Gregory M Cooper, Troy Zerr, Joshua D Smith, Carl Baker, Neil Shafer, Erik C Thorland, Cindy Skinner, Charles E Schwartz, Deborah A Nickerson,[...]. Genome Res 2009
102
20

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
20

Copy Number Variations with Isolated Fetal Ventriculomegaly.
P Hu, Y Wang, R Sun, L Cao, X Chen, C Liu, C Luo, D Ma, W Wang, X Fu,[...]. Curr Mol Med 2017
11
20

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
10

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
10

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
10

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
10

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
10

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
12

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
10

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
10

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
10

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
10

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
10

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
10

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
10

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
10

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
10

The 15q11.2 BP1-BP2 microdeletion syndrome: a review.
Devin M Cox, Merlin G Butler. Int J Mol Sci 2015
94
10

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
10

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
10


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
10

Intrauterine phenotypic features associated with 16p11.2 recurrent microdeletions.
Shaobin Lin, Shanshan Shi, Yi Zhou, Yuanjun Ji, Peizhi Huang, Jianzhu Wu, Baojiang Chen, Yanmin Luo. Prenat Diagn 2018
4
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
10

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
10

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
10

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
10

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
10

Association study in siblings and case-controls of serotonin- and oxytocin-related genes with high functioning autism.
Johanna Nyffeler, Susanne Walitza, Elise Bobrowski, Ronnie Gundelfinger, Edna Grünblatt. J Mol Psychiatry 2014
30
10

Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments.
Claire S Leblond, Caroline Nava, Anne Polge, Julie Gauthier, Guillaume Huguet, Serge Lumbroso, Fabienne Giuliano, Coline Stordeur, Christel Depienne, Kevin Mouzat,[...]. PLoS Genet 2014
280
10

FARP2, HDLBP and PASK are downregulated in a patient with autism and 2q37.3 deletion syndrome.
Bärbel Felder, Bernhard Radlwimmer, Axel Benner, Antoaneta Mincheva, Grischa Tödt, Kim S Beyer, Claudia Schuster, Sven Bölte, Gabriele Schmötzer, Sabine M Klauck,[...]. Am J Med Genet A 2009
28
10



Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.
Stephan J Sanders, A Gulhan Ercan-Sencicek, Vanessa Hus, Rui Luo, Michael T Murtha, Daniel Moreno-De-Luca, Su H Chu, Michael P Moreau, Abha R Gupta, Susanne A Thomson,[...]. Neuron 2011
802
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.