A citation-based method for searching scientific literature

Stuart A Scott, Ninette Cohen, Tracy Brandt, Gokce Toruner, Robert J Desnick, Lisa Edelmann. Genet Med 2010
Times Cited: 63







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



Times Cited
  Times     Co-cited
Similarity


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
207
41

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
129
36

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
34

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
265
22

Comparison of microarray-based detection rates for cytogenetic abnormalities in prenatal and neonatal specimens.
Lisa G Shaffer, Justine Coppinger, Sarah Alliman, Beth A Torchia, Aaron Theisen, Blake C Ballif, Bassem A Bejjani. Prenat Diagn 2008
89
17

Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases.
Ignatia B Van den Veyver, Ankita Patel, Chad A Shaw, Amber N Pursley, Sung-Hae L Kang, Marcia J Simovich, Patricia A Ward, Sandra Darilek, Anthony Johnson, Sarah E Neill,[...]. Prenat Diagn 2009
139
17

Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysis.
S C Hillman, S Pretlove, A Coomarasamy, D J McMullan, E V Davison, E R Maher, M D Kilby. Ultrasound Obstet Gynecol 2011
154
17

Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports.
B Menten, N Maas, B Thienpont, K Buysse, J Vandesompele, C Melotte, T de Ravel, S Van Vooren, I Balikova, L Backx,[...]. J Med Genet 2006
313
15

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
15

Global variation in copy number in the human genome.
Richard Redon, Shumpei Ishikawa, Karen R Fitch, Lars Feuk, George H Perry, T Daniel Andrews, Heike Fiegler, Michael H Shapero, Andrew R Carson, Wenwei Chen,[...]. Nature 2006
14


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
14

Detection of mosaicism for genome imbalance in a cohort of 3,042 clinical cases using an oligonucleotide array CGH platform.
Sarah Hoang, Joowook Ahn, Kathy Mann, Sue Bint, Sahar Mansour, Tessa Homfray, Shehla Mohammed, Caroline Mackie Ogilvie. Eur J Med Genet 2011
26
34

Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization.
Trilochan Sahoo, Sau Wai Cheung, Patricia Ward, Sandra Darilek, Ankita Patel, Daniela del Gaudio, Sung Hae L Kang, Seema R Lalani, Jiangzhen Li, Sallie McAdoo,[...]. Genet Med 2006
122
12

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
12



Comparative genomic hybridization-array analysis enhances the detection of aneuploidies and submicroscopic imbalances in spontaneous miscarriages.
Anthony J Schaeffer, June Chung, Konstantina Heretis, Andrew Wong, David H Ledbetter, Christa Lese Martin. Am J Hum Genet 2004
146
11

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
11

Diagnostic utility of array-based comparative genomic hybridization (aCGH) in a prenatal setting.
Idit Maya, Bella Davidov, Liron Gershovitz, Yael Zalzstein, Ellen Taub, Justine Coppinger, Lisa G Shaffer, Mordechai Shohat. Prenat Diagn 2010
63
11


Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells.
Roberto Valli, Cristina Marletta, Barbara Pressato, Giuseppe Montalbano, Francesco Lo Curto, Francesco Pasquali, Emanuela Maserati. Mol Cytogenet 2011
31
22

Breakpoint mapping and array CGH in translocations: comparison of a phenotypically normal and an abnormal cohort.
Julia Baptista, Catherine Mercer, Elena Prigmore, Susan M Gribble, Nigel P Carter, Viv Maloney, N Simon Thomas, Patricia A Jacobs, John A Crolla. Am J Hum Genet 2008
115
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
417
9



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
182
9

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
9

Prenatal detection of unbalanced chromosomal rearrangements by array CGH.
L Rickman, H Fiegler, C Shaw-Smith, R Nash, V Cirigliano, G Voglino, B L Ng, C Scott, J Whittaker, M Adinolfi,[...]. J Med Genet 2006
94
9

Pre- and postnatal genetic testing by array-comparative genomic hybridization: genetic counseling perspectives.
Sandra Darilek, Patricia Ward, Amber Pursley, Katie Plunkett, Patti Furman, Pilar Magoulas, Ankita Patel, Sau Wai Cheung, Christine M Eng. Genet Med 2008
58
10

Current controversies in prenatal diagnosis 3: is conventional chromosome analysis necessary in the post-array CGH era?
The-Hung Bui, Annalisa Vetro, Orsetta Zuffardi, Lisa G Shaffer. Prenat Diagn 2011
39
15


Detecting sex chromosome anomalies and common triploidies in products of conception by array-based comparative genomic hybridization.
Blake C Ballif, Catherine D Kashork, Reza Saleki, Emily Rorem, Kyle Sundin, Bassem A Bejjani, Lisa G Shaffer. Prenat Diagn 2006
42
14

Microarray analysis for constitutional cytogenetic abnormalities.
Lisa G Shaffer, Arthur L Beaudet, Arthur R Brothman, Betsy Hirsch, Brynn Levy, Christa Lese Martin, James T Mascarello, Kathleen W Rao. Genet Med 2007
50
10

Genomic imbalances in neonates with birth defects: high detection rates by using chromosomal microarray analysis.
Xin-Yan Lu, Mai T Phung, Chad A Shaw, Kim Pham, Sarah E Neil, Ankita Patel, Trilochan Sahoo, Carlos A Bacino, Pawel Stankiewicz, Sung-Hae Lee Kang,[...]. Pediatrics 2008
106
7

Clinical implementation of chromosomal microarray analysis: summary of 2513 postnatal cases.
Xinyan Lu, Chad A Shaw, Ankita Patel, Jiangzhen Li, M Lance Cooper, William R Wells, Cathy M Sullivan, Trilochan Sahoo, Svetlana A Yatsenko, Carlos A Bacino,[...]. PLoS One 2007
159
7

Variability in interpreting and reporting copy number changes detected by array-based technology in clinical laboratories.
Karen D Tsuchiya, Lisa G Shaffer, Swaroop Aradhya, Julie M Gastier-Foster, Ankita Patel, M Katharine Rudd, Julie Sanford Biggerstaff, Warren G Sanger, Stuart Schwartz, James H Tepperberg,[...]. Genet Med 2009
41
12

Copy number variations and clinical cytogenetic diagnosis of constitutional disorders.
Charles Lee, A John Iafrate, Arthur R Brothman. Nat Genet 2007
270
7

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
103
7

Use of targeted array-based CGH for the clinical diagnosis of chromosomal imbalance: is less more?
Bassem A Bejjani, Reza Saleki, Blake C Ballif, Emily A Rorem, Kyle Sundin, Aaron Theisen, Catherine D Kashork, Lisa G Shaffer. Am J Med Genet A 2005
160
7

Structural variation in the human genome.
Lars Feuk, Andrew R Carson, Stephen W Scherer. Nat Rev Genet 2006
7

Mapping and sequencing of structural variation from eight human genomes.
Jeffrey M Kidd, Gregory M Cooper, William F Donahue, Hillary S Hayden, Nick Sampas, Tina Graves, Nancy Hansen, Brian Teague, Can Alkan, Francesca Antonacci,[...]. Nature 2008
765
7

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
7

Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification.
Jan P Schouten, Cathal J McElgunn, Raymond Waaijer, Danny Zwijnenburg, Filip Diepvens, Gerard Pals. Nucleic Acids Res 2002
7

Comparative analysis of copy number detection by whole-genome BAC and oligonucleotide array CGH.
Nicholas J Neill, Beth S Torchia, Bassem A Bejjani, Lisa G Shaffer, Blake C Ballif. Mol Cytogenet 2010
45
11

Validation and implementation of array comparative genomic hybridisation as a first line test in place of postnatal karyotyping for genome imbalance.
Joo Wook Ahn, Kathy Mann, Sally Walsh, Marwa Shehab, Sarah Hoang, Zoe Docherty, Shehla Mohammed, Caroline Mackie Ogilvie. Mol Cytogenet 2010
43
11

Introducing array comparative genomic hybridization into routine prenatal diagnosis practice: a prospective study on over 1000 consecutive clinical cases.
Francesco Fiorentino, Fiorina Caiazzo, Stefania Napolitano, Letizia Spizzichino, Sara Bono, Mariateresa Sessa, Andrea Nuccitelli, Anil Biricik, Anthony Gordon, Giuseppe Rizzo,[...]. Prenat Diagn 2011
75
7

Clinical utility of chromosomal microarray analysis in invasive prenatal diagnosis.
Lluís Armengol, Julián Nevado, Clara Serra-Juhé, Alberto Plaja, Carmen Mediano, Fe Amalia García-Santiago, Manel García-Aragonés, Olaya Villa, Elena Mansilla, Cristina Preciado,[...]. Hum Genet 2012
61
8

Experience with microarray-based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnancies.
Lisa G Shaffer, Mindy P Dabell, Allan J Fisher, Justine Coppinger, Anne M Bandholz, Jay W Ellison, J Britt Ravnan, Beth S Torchia, Blake C Ballif, Jill A Rosenfeld. Prenat Diagn 2012
136
7

High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications.
Tamim H Shaikh, Xiaowu Gai, Juan C Perin, Joseph T Glessner, Hongbo Xie, Kevin Murphy, Ryan O'Hara, Tracy Casalunovo, Laura K Conlin, Monica D'Arcy,[...]. Genome Res 2009
282
7


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.