A citation-based method for searching scientific literature

N de Leeuw, J Y Hehir-Kwa, A Simons, A Geurts van Kessel, D F Smeets, B H W Faas, R Pfundt. Cytogenet Genome Res 2011
Times Cited: 31







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



Times Cited
  Times     Co-cited
Similarity


Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein,[...]. Am J Hum Genet 2010
25

European Cytogeneticists Association Register of Unbalanced Chromosome Aberrations (ECARUCA); an online database for rare chromosome abnormalities.
I Feenstra, J Fang, D A Koolen, A Siezen, C Evans, R M Winter, M M Lees, M Riegel, B B A de Vries, C M A Van Ravenswaaij,[...]. Eur J Med Genet 2006
60
19

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
972
19

American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants.
Hutton M Kearney, Erik C Thorland, Kerry K Brown, Fabiola Quintero-Rivera, Sarah T South. Genet Med 2011
533
16

A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays.
Yasuhito Nannya, Masashi Sanada, Kumi Nakazaki, Noriko Hosoya, Lili Wang, Akira Hangaishi, Mineo Kurokawa, Shigeru Chiba, Dione K Bailey, Giulia C Kennedy,[...]. Cancer Res 2005
553
12

Guidelines for molecular karyotyping in constitutional genetic diagnosis.
Joris Robert Vermeesch, Heike Fiegler, Nicole de Leeuw, Karoly Szuhai, Jacqueline Schoumans, Roberto Ciccone, Frank Speleman, Anita Rauch, Jill Clayton-Smith, Conny Van Ravenswaaij,[...]. Eur J Hum Genet 2007
102
12

Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis.
Laura K Conlin, Brian D Thiel, Carsten G Bonnemann, Livija Medne, Linda M Ernst, Elaine H Zackai, Matthew A Deardorff, Ian D Krantz, Hakon Hakonarson, Nancy B Spinner. Hum Mol Genet 2010
270
12

Diagnostic interpretation of array data using public databases and internet sources.
Nicole de Leeuw, Trijnie Dijkhuizen, Jayne Y Hehir-Kwa, Nigel P Carter, Lars Feuk, Helen V Firth, Robert M Kuhn, David H Ledbetter, Christa Lese Martin, Conny M A van Ravenswaaij-Arts,[...]. Hum Mutat 2012
70
12

Genome-wide arrays in routine diagnostics of hematological malignancies.
Annet Simons, Birgit Sikkema-Raddatz, Nicole de Leeuw, Nicole Claudia Konrad, Rosalind J Hastings, Jacqueline Schoumans. Hum Mutat 2012
36
12

Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformations.
C Le Caignec, M Boceno, P Saugier-Veber, S Jacquemont, M Joubert, A David, T Frebourg, J M Rival. J Med Genet 2005
147
12

Challenges for CNV interpretation in clinical molecular karyotyping: lessons learned from a 1001 sample experience.
Karen Buysse, Barbara Delle Chiaie, Rudy Van Coster, Bart Loeys, Anne De Paepe, Geert Mortier, Frank Speleman, Björn Menten. Eur J Med Genet 2009
73
9

Detection of low-level mosaicism by array CGH in routine diagnostic specimens.
Blake C Ballif, Emily A Rorem, Kyle Sundin, Matt Lincicum, Shannon Gaskin, Justine Coppinger, Catherine D Kashork, Lisa G Shaffer, Bassem A Bejjani. Am J Med Genet A 2006
208
9

A copy number variation morbidity map of developmental delay.
Gregory M Cooper, Bradley P Coe, Santhosh Girirajan, Jill A Rosenfeld, Tiffany H Vu, Carl Baker, Charles Williams, Heather Stalker, Rizwan Hamid, Vickie Hannig,[...]. Nat Genet 2011
820
9

Population analysis of large copy number variants and hotspots of human genetic disease.
Andy Itsara, Gregory M Cooper, Carl Baker, Santhosh Girirajan, Jun Li, Devin Absher, Ronald M Krauss, Richard M Myers, Paul M Ridker, Daniel I Chasman,[...]. Am J Hum Genet 2009
420
9


Copy number variations and clinical cytogenetic diagnosis of constitutional disorders.
Charles Lee, A John Iafrate, Arthur R Brothman. Nat Genet 2007
269
9

Array comparative genomic hybridization in prenatal diagnosis: another experience.
F Vialard, D Molina Gomes, B Leroy, E Quarello, A Escalona, C Le Sciellour, V Serazin, J Roume, Y Ville, P de Mazancourt,[...]. Fetal Diagn Ther 2009
58
9


Updates in cytogenetics and molecular markers in MDS.
Ramon V Tiu, Valeria Visconte, Fabiola Traina, Anita Schwandt, Jaroslaw P Maciejewski. Curr Hematol Malig Rep 2011
33
9

Genome-wide arrays: quality criteria and platforms to be used in routine diagnostics.
Joris R Vermeesch, Paul D Brady, Damien Sanlaville, Klaas Kok, Rosalind J Hastings. Hum Mutat 2012
54
9

A de novo paradigm for mental retardation.
Lisenka E L M Vissers, Joep de Ligt, Christian Gilissen, Irene Janssen, Marloes Steehouwer, Petra de Vries, Bart van Lier, Peer Arts, Nienke Wieskamp, Marisol del Rosario,[...]. Nat Genet 2010
556
9

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
Brian J O'Roak, Pelagia Deriziotis, Choli Lee, Laura Vives, Jerrod J Schwartz, Santhosh Girirajan, Emre Karakoc, Alexandra P Mackenzie, Sarah B Ng, Carl Baker,[...]. Nat Genet 2011
775
9

Genomic microarrays in mental retardation: from copy number variation to gene, from research to diagnosis.
Lisenka E L M Vissers, Bert B A de Vries, Joris A Veltman. J Med Genet 2010
107
9

Mapping copy number variation by population-scale genome sequencing.
Ryan E Mills, Klaudia Walter, Chip Stewart, Robert E Handsaker, Ken Chen, Can Alkan, Alexej Abyzov, Seungtai Chris Yoon, Kai Ye, R Keira Cheetham,[...]. Nature 2011
714
9

Origins and functional impact of copy number variation in the human genome.
Donald F Conrad, Dalila Pinto, Richard Redon, Lars Feuk, Omer Gokcumen, Yujun Zhang, Jan Aerts, T Daniel Andrews, Chris Barnes, Peter Campbell,[...]. Nature 2010
9

Large-scale copy number polymorphism in the human genome.
Jonathan Sebat, B Lakshmi, Jennifer Troge, Joan Alexander, Janet Young, Pär Lundin, Susanne Månér, Hillary Massa, Megan Walker, Maoyen Chi,[...]. Science 2004
9

Detection of large-scale variation in the human genome.
A John Iafrate, Lars Feuk, Miguel N Rivera, Marc L Listewnik, Patricia K Donahoe, Ying Qi, Stephen W Scherer, Charles Lee. Nat Genet 2004
9

Single-nucleotide polymorphism array karyotyping in clinical practice: where, when, and how?
Aiko Sato-Otsubo, Masashi Sanada, Seishi Ogawa. Semin Oncol 2012
23
13

An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities.
Erin B Kaminsky, Vineith Kaul, Justin Paschall, Deanna M Church, Brian Bunke, Dawn Kunig, Daniel Moreno-De-Luca, Andres Moreno-De-Luca, Jennifer G Mulle, Stephen T Warren,[...]. Genet Med 2011
290
6

Circular binary segmentation for the analysis of array-based DNA copy number data.
Adam B Olshen, E S Venkatraman, Robert Lucito, Michael Wigler. Biostatistics 2004
6

Microarray-based CGH detects chromosomal mosaicism not revealed by conventional cytogenetics.
Sau W Cheung, Chad A Shaw, Daryl A Scott, Ankita Patel, Trilochan Sahoo, Carlos A Bacino, Amber Pursley, Jiangzhen Li, Robert Erickson, Andrea L Gropman,[...]. Am J Med Genet A 2007
130
6

Deletions in the VPS13B (COH1) gene as a cause of Cohen syndrome.
I Balikova, A-E Lehesjoki, T J L de Ravel, B Thienpont, K E Chandler, J Clayton-Smith, A-L Träskelin, J-P Fryns, J R Vermeesch. Hum Mutat 2009
41
6



Detection of clinically relevant exonic copy-number changes by array CGH.
Philip M Boone, Carlos A Bacino, Chad A Shaw, Patricia A Eng, Patricia M Hixson, Amber N Pursley, Sung-Hae L Kang, Yaping Yang, Joanna Wiszniewska, Beata A Nowakowska,[...]. Hum Mutat 2010
185
6

Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype.
G D'Amours, Z Kibar, G Mathonnet, R Fetni, F Tihy, V Désilets, S Nizard, J L Michaud, E Lemyre. Clin Genet 2012
58
6

High resolution array analysis: diagnosing pregnancies with abnormal ultrasound findings.
M Tyreman, K M Abbott, L R Willatt, R Nash, C Lees, J Whittaker, I Simonic. J Med Genet 2009
90
6

Use of array comparative genomic hybridization for prenatal diagnosis of fetuses with sonographic anomalies and normal metaphase karyotype.
Linda Kleeman, Diana W Bianchi, Lisa G Shaffer, Emily Rorem, Janet Cowan, Sabrina D Craigo, Hocine Tighiouart, Louise E Wilkins-Haug. Prenat Diagn 2009
78
6

SNP array analysis in hematologic malignancies: avoiding false discoveries.
Stefan Heinrichs, Cheng Li, A Thomas Look. Blood 2010
70
6


Prognostic impact of SNP array karyotyping in myelodysplastic syndromes and related myeloid malignancies.
Ramon V Tiu, Lukasz P Gondek, Christine L O'Keefe, Paul Elson, Jungwon Huh, Azim Mohamedali, Austin Kulasekararaj, Anjali S Advani, Ronald Paquette, Alan F List,[...]. Blood 2011
147
6

Public data archives for genomic structural variation.
Deanna M Church, Ilkka Lappalainen, Tam P Sneddon, Jonathan Hinton, Michael Maguire, John Lopez, John Garner, Justin Paschall, Michael DiCuccio, Eugene Yaschenko,[...]. Nat Genet 2010
63
6

New lesions detected by single nucleotide polymorphism array-based chromosomal analysis have important clinical impact in acute myeloid leukemia.
Ramon V Tiu, Lukasz P Gondek, Christine L O'Keefe, Jungwon Huh, Mikkael A Sekeres, Paul Elson, Michael A McDevitt, Xiao Fei Wang, Mark J Levis, Judith E Karp,[...]. J Clin Oncol 2009
95
6

Implementation of high resolution single nucleotide polymorphism array analysis as a clinical test for patients with hematologic malignancies.
Margaret J Dougherty, Donna M Wilmoth, Laura S Tooke, Tamim H Shaikh, Xiaowu Gai, Hakon Hakonarson, Jaclyn A Biegel. Cancer Genet 2011
27
7

Functional impact of global rare copy number variation in autism spectrum disorders.
Dalila Pinto, Alistair T Pagnamenta, Lambertus Klei, Richard Anney, Daniele Merico, Regina Regan, Judith Conroy, Tiago R Magalhaes, Catarina Correia, Brett S Abrahams,[...]. Nature 2010
6

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.
Joseph T Glessner, Kai Wang, Guiqing Cai, Olena Korvatska, Cecilia E Kim, Shawn Wood, Haitao Zhang, Annette Estes, Camille W Brune, Jonathan P Bradfield,[...]. Nature 2009
935
6

Strong association of de novo copy number mutations with autism.
Jonathan Sebat, B Lakshmi, Dheeraj Malhotra, Jennifer Troge, Christa Lese-Martin, Tom Walsh, Boris Yamrom, Seungtai Yoon, Alex Krasnitz, Jude Kendall,[...]. Science 2007
6

Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome.
B W M van Bon, H C Mefford, B Menten, D A Koolen, A J Sharp, W M Nillesen, J W Innis, T J L de Ravel, C L Mercer, M Fichera,[...]. J Med Genet 2009
202
6

High resolution analysis of follicular lymphoma genomes reveals somatic recurrent sites of copy-neutral loss of heterozygosity and copy number alterations that target single genes.
K-John J Cheung, Allen Delaney, Susana Ben-Neriah, Jacquie Schein, Tang Lee, Sohrab P Shah, Dorothy Cheung, Nathalie A Johnson, Andrew J Mungall, Adele Telenius,[...]. Genes Chromosomes Cancer 2010
34
6

Genome-wide mapping of copy number variation in humans: comparative analysis of high resolution array platforms.
Rajini R Haraksingh, Alexej Abyzov, Mark Gerstein, Alexander E Urban, Michael Snyder. PLoS One 2011
43
6


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.