A citation-based method for searching scientific literature

Lisa G Shaffer, Jill A Rosenfeld. Expert Rev Mol Diagn 2013
Times Cited: 13







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



Times Cited
  Times     Co-cited
Similarity


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
664
53

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
46

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
30

Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysis.
S C Hillman, D J McMullan, G Hall, F S Togneri, N James, E J Maher, C H Meller, D Williams, R J Wapner, E R Maher,[...]. Ultrasound Obstet Gynecol 2013
158
30


Copy number and SNP arrays in clinical diagnostics.
Christian P Schaaf, Joanna Wiszniewska, Arthur L Beaudet. Annu Rev Genomics Hum Genet 2011
101
23

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
23

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
15


Quantitative fluorescence PCR analysis of >40,000 prenatal samples for the rapid diagnosis of trisomies 13, 18 and 21 and monosomy X.
Kathy Mann, Alison Hills, Celia Donaghue, Helen Thomas, Caroline Mackie Ogilvie. Prenat Diagn 2012
22
15


Enhanced detection of clinically relevant genomic imbalances using a targeted plus whole genome oligonucleotide microarray.
Erin L Baldwin, Ji-Yun Lee, Douglas M Blake, Brian P Bunke, Chad R Alexander, Amy L Kogan, David H Ledbetter, Christa L Martin. Genet Med 2008
125
15


Chromosomal microarray analysis as a first-line test in pregnancies with a priori low risk for the detection of submicroscopic chromosomal abnormalities.
Francesco Fiorentino, Stefania Napoletano, Fiorina Caiazzo, Mariateresa Sessa, Sara Bono, Letizia Spizzichino, Anthony Gordon, Andrea Nuccitelli, Giuseppe Rizzo, Marina Baldi. Eur J Hum Genet 2013
62
15


Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literature.
Amy Breman, Amber N Pursley, Patricia Hixson, Weimin Bi, Patricia Ward, Carlos A Bacino, Chad Shaw, James R Lupski, Arthur Beaudet, Ankita Patel,[...]. Prenat Diagn 2012
77
15

Copy-number variations, noncoding sequences, and human phenotypes.
Eva Klopocki, Stefan Mundlos. Annu Rev Genomics Hum Genet 2011
42
15

Frequent detection of parental consanguinity in children with developmental disorders by a combined CGH and SNP microarray.
Yao-Shan Fan, Xiaomei Ouyang, Jinghong Peng, Stephanie Sacharow, Mustafa Tekin, Deborah Barbouth, Olaf Bodamer, Roman Yusupov, Christina Navarrete, Ana H Heller,[...]. Mol Cytogenet 2013
18
15

Maternal mosaicism is a significant contributor to discordant sex chromosomal aneuploidies associated with noninvasive prenatal testing.
Yanlin Wang, Yan Chen, Feng Tian, Jianguang Zhang, Zhuo Song, Yi Wu, Xu Han, Wenjing Hu, Duan Ma, David Cram,[...]. Clin Chem 2014
146
15

Traditional karyotyping vs copy number variation sequencing for detection of chromosomal abnormalities associated with spontaneous miscarriage.
S Liu, L Song, D S Cram, L Xiong, K Wang, R Wu, J Liu, K Deng, B Jia, M Zhong,[...]. Ultrasound Obstet Gynecol 2015
39
15

Copy number variation sequencing for comprehensive diagnosis of chromosome disease syndromes.
Desheng Liang, Ying Peng, Weigang Lv, Linbei Deng, Yanghui Zhang, Haoxian Li, Pu Yang, Jianguang Zhang, Zhuo Song, Genming Xu,[...]. J Mol Diagn 2014
68
15

College of American Pathologists/American College of Medical Genetics proficiency testing for constitutional cytogenomic microarray analysis.
Arthur R Brothman, Michelle M Dolan, Barbara K Goodman, Jonathan P Park, Diane L Persons, Debra F Saxe, James H Tepperberg, Karen D Tsuchiya, Daniel L Van Dyke, Kathleen S Wilson,[...]. Genet Med 2011
9
22

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
15

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
156
15

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
15

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
15

Regions of homozygosity identified by oligonucleotide SNP arrays: evaluating the incidence and clinical utility.
Jia-Chi Wang, Leslie Ross, Loretta W Mahon, Renius Owen, Morteza Hemmat, Boris T Wang, Mohammed El Naggar, Kimberly A Kopita, Linda M Randolph, John M Chase,[...]. Eur J Hum Genet 2015
29
15



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
96
7

Maternal serum screening for Down's syndrome in early pregnancy.
N J Wald, H S Cuckle, J W Densem, K Nanchahal, P Royston, T Chard, J E Haddow, G J Knight, G E Palomaki, J A Canick. BMJ 1988
756
7

Prenatal diagnosis using array-CGH: a French experience.
Caroline Rooryck, Jérôme Toutain, Dorothée Cailley, Julie Bouron, Jacques Horovitz, Didier Lacombe, Benoit Arveiler, Robert Saura. Eur J Med Genet 2013
28
7

Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities.
Lisenka E L M Vissers, Bert B A de Vries, Kazutoyo Osoegawa, Irene M Janssen, Ton Feuth, Chik On Choy, Huub Straatman, Walter van der Vliet, Erik H L P G Huys, Anke van Rijk,[...]. Am J Hum Genet 2003
345
7

Microarrays as a diagnostic tool in prenatal screening strategies: ethical reflection.
Antina de Jong, Wybo J Dondorp, Merryn V E Macville, Christine E M de Die-Smulders, Jan M M van Lith, Guido M W R de Wert. Hum Genet 2014
26
7

Rapid aneuploidy detection or karyotyping? Ethical reflection.
Antina de Jong, Wybo J Dondorp, Daniëlle R M Timmermans, Jan M M van Lith, Guido M W R de Wert. Eur J Hum Genet 2011
10
10

Intrauterine diagnosis and management of genetic defects.
C B Jacobson, R H Barter. Am J Obstet Gynecol 1967
190
7



An overview of a 30-year experience with amniocentesis in a single tertiary medical center in Taiwan.
Yi-Wen Chang, Chia-Ming Chang, Pi-Lin Sung, Ming-Jie Yang, Wai Hou Li, Hsin-Yang Li, Ling-Chao Chen, Ling-Yi Cheng, Yu-Ling Lai, Yung-Yung Cheng,[...]. Taiwan J Obstet Gynecol 2012
26
7

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
76
7


Prenatal diagnosis by array-CGH.
L Rickman, H Fiegler, N P Carter, M Bobrow. Eur J Med Genet 2005
42
7

Meeting the challenge of interpreting high-resolution single nucleotide polymorphism array data in prenatal diagnosis: does increased diagnostic power outweigh the dilemma of rare variants?
D Ganesamoorthy, D L Bruno, G McGillivray, F Norris, S M White, S Adroub, D J Amor, A Yeung, R Oertel, M D Pertile,[...]. BJOG 2013
28
7

Prenatal chromosomal microarray analysis: a survey of prenatal genetic counselors' experiences and attitudes.
Marina Mikhaelian, Patricia McCarthy Veach, Ian MacFarlane, Bonnie S LeRoy, Matthew Bower. Prenat Diagn 2013
18
7

Efficient direct chromosome analyses and enzyme determinations from chorionic villi samples in the first trimester of pregnancy.
G Simoni, B Brambati, C Danesino, F Rossella, G L Terzoli, M Ferrari, M Fraccaro. Hum Genet 1983
447
7

Clinical and cytogenetic findings on 31,615 mid-trimester amniocenteses.
Sung-Hee Han, Jeong-Wook An, Gyu-Young Jeong, Hye-Ryoung Yoon, Anna Lee, Young-Ho Yang, Kyu-Pum Lee, Kyoung-Ryul Lee. Korean J Lab Med 2008
28
7

Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities.
Malgorzata I Srebniak, Marjan Boter, Gretel O Oudesluijs, Titia Cohen-Overbeek, Lutgarde Cp Govaerts, Karin Em Diderich, Renske Oegema, Maarten Fcm Knapen, Ingrid Mbh van de Laar, Marieke Joosten,[...]. Mol Cytogenet 2012
52
7

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
7

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
7

The introduction of arrays in prenatal diagnosis: a special challenge.
Annalisa Vetro, Katelijne Bouman, Ros Hastings, Dominic J McMullan, Joris R Vermeesch, Konstantin Miller, Birgit Sikkema-Raddatz, David H Ledbetter, Orsetta Zuffardi, Conny M A van Ravenswaaij-Arts. Hum Mutat 2012
52
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.