A citation-based method for searching scientific literature

Melissa Stosic, Brynn Levy, Ronald Wapner. Obstet Gynecol Clin North Am 2018
Times Cited: 23







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



Times Cited
  Times     Co-cited
Similarity


Prenatal diagnosis by chromosomal microarray analysis.
Brynn Levy, Ronald Wapner. Fertil Steril 2018
105
52

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
690
43

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
165
21


The use of chromosomal microarray for prenatal diagnosis.
Lorraine Dugoff, Mary E Norton, Jeffrey A Kuller. Am J Obstet Gynecol 2016
65
21

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
17

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
549
17

Procedure-related risk of miscarriage following amniocentesis and chorionic villus sampling: a systematic review and meta-analysis.
R Akolekar, J Beta, G Picciarelli, C Ogilvie, F D'Antonio. Ultrasound Obstet Gynecol 2015
339
17

ACOG and SMFM guidelines for prenatal diagnosis: Is karyotyping really sufficient?
Sara B Hay, Trilochan Sahoo, Mary K Travis, Karine Hovanes, Natasa Dzidic, Charles Doherty, Michelle N Strecker. Prenat Diagn 2018
37
17

Microarrays in prenatal diagnosis.
Beatrice Oneda, Anita Rauch. Best Pract Res Clin Obstet Gynaecol 2017
24
17

Nasal bone assessment in prenatal screening for trisomy 21.
J D Sonek, S Cicero, R Neiger, K H Nicolaides. Am J Obstet Gynecol 2006
79
13

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
142
13

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
38
13


Genomic microarray in fetuses with increased nuchal translucency and normal karyotype: a systematic review and meta-analysis.
M Grande, F A R Jansen, Y J Blumenfeld, A Fisher, A O Odibo, M C Haak, A Borrell. Ultrasound Obstet Gynecol 2015
90
13


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
162
13

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
79
13

Practice guideline: joint CCMG-SOGC recommendations for the use of chromosomal microarray analysis for prenatal diagnosis and assessment of fetal loss in Canada.
Christine M Armour, Shelley Danielle Dougan, Jo-Ann Brock, Radha Chari, Bernie N Chodirker, Isabelle DeBie, Jane A Evans, William T Gibson, Elena Kolomietz, Tanya N Nelson,[...]. J Med Genet 2018
37
13

The role of ultrasound in women who undergo cell-free DNA screening.
Mary E Norton, Joseph R Biggio, Jeffrey A Kuller, Sean C Blackwell. Am J Obstet Gynecol 2017
53
8


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
8

Genome structural variation discovery and genotyping.
Can Alkan, Bradley P Coe, Evan E Eichler. Nat Rev Genet 2011
782
8

Meta-analysis of second-trimester markers for trisomy 21.
M Agathokleous, P Chaveeva, L C Y Poon, P Kosinski, K H Nicolaides. Ultrasound Obstet Gynecol 2013
129
8

Prenatal SNP array testing in 1000 fetuses with ultrasound anomalies: causative, unexpected and susceptibility CNVs.
Malgorzata I Srebniak, Karin Em Diderich, Marieke Joosten, Lutgarde Cp Govaerts, Jeroen Knijnenburg, Femke At de Vries, Marjan Boter, Debora Lont, Maarten Fcm Knapen, Merel C de Wit,[...]. Eur J Hum Genet 2016
44
8


Update on the use of exome sequencing in the diagnosis of fetal abnormalities.
Lauren Ferretti, Rhiannon Mellis, Lyn S Chitty. Eur J Med Genet 2019
23
8



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
18
11

Diagnostic yield of chromosomal microarray analysis in fetuses with isolated increased nuchal translucency: a French multicenter study.
M Egloff, B Hervé, T Quibel, S Jaillard, G Le Bouar, K Uguen, A-H Saliou, M Valduga, E Perdriolle, C Coutton,[...]. Ultrasound Obstet Gynecol 2018
23
8

From karyotyping to array-CGH in prenatal diagnosis.
K D Lichtenbelt, N V A M Knoers, G H Schuring-Blom. Cytogenet Genome Res 2011
39
8

The frequency of the detection of fetal echogenic intracardiac foci with respect to maternal race.
T D Shipp, B Bromley, E Lieberman, B R Benacerraf. Ultrasound Obstet Gynecol 2000
61
8

The importance of copy number variation in congenital heart disease.
Gregory Costain, Candice K Silversides, Anne S Bassett. NPJ Genom Med 2016
31
8

Amniocentesis and chorionic villus sampling for prenatal diagnosis.
Zarko Alfirevic, Kate Navaratnam, Faris Mujezinovic. Cochrane Database Syst Rev 2017
57
8

An isolated intracardiac echogenic focus as a marker for aneuploidy.
Kathleen E Bradley, Thomas S Santulli, Kimberly D Gregory, William Herbert, Dru E Carlson, Lawrence D Platt. Am J Obstet Gynecol 2005
23
8



Randomised controlled trial of genetic amniocentesis in 4606 low-risk women.
A Tabor, J Philip, M Madsen, J Bang, E B Obel, B Nørgaard-Pedersen. Lancet 1986
594
8

Microdeletion and microduplication syndromes.
Anja Weise, Kristin Mrasek, Elisabeth Klein, Milene Mulatinho, Juan C Llerena, David Hardekopf, Sona Pekova, Samarth Bhatt, Nadezda Kosyakova, Thomas Liehr. J Histochem Cytochem 2012
79
8


ISUOG Practice Guidelines: invasive procedures for prenatal diagnosis.
T Ghi, A Sotiriadis, P Calda, F Da Silva Costa, N Raine-Fenning, Z Alfirevic, G McGillivray. Ultrasound Obstet Gynecol 2016
50
8

Identification of copy number variations associated with congenital heart disease by chromosomal microarray analysis and next-generation sequencing.
Xiangyu Zhu, Jie Li, Tong Ru, Yaping Wang, Yan Xu, Ying Yang, Xing Wu, David S Cram, Yali Hu. Prenat Diagn 2016
45
8


A prospective study of the clinical utility of prenatal chromosomal microarray analysis in fetuses with ultrasound abnormalities and an exploration of a framework for reporting unclassified variants and risk factors.
Paul Daniel Brady, Barbara Delle Chiaie, Gabrielle Christenhusz, Kris Dierickx, Kris Van Den Bogaert, Bjorn Menten, Sandra Janssens, Paul Defoort, Ellen Roets, Elke Sleurs,[...]. Genet Med 2014
50
8

Traditional banding of chromosomes for cytogenetic analysis.
Jane Bayani, Jeremy A Squire. Curr Protoc Cell Biol 2004
13
15

SNP microarray-based 24 chromosome aneuploidy screening is significantly more consistent than FISH.
Nathan R Treff, Brynn Levy, Jing Su, Lesley E Northrop, Xin Tao, Richard T Scott. Mol Hum Reprod 2010
114
8

Genomics-based non-invasive prenatal testing for detection of fetal chromosomal aneuploidy in pregnant women.
Mylène Badeau, Carmen Lindsay, Jonatan Blais, Leon Nshimyumukiza, Yemisi Takwoingi, Sylvie Langlois, France Légaré, Yves Giguère, Alexis F Turgeon, William Witteman,[...]. Cochrane Database Syst Rev 2017
37
8

Prenatal BACs-on-Beads™: the prospective experience of five prenatal diagnosis laboratories.
François Vialard, Giuseppe Simoni, Denise Molina Gomes, Azzedine Abourra, Simona De Toffol, Fabrice Bru, Maria Carmen Martinez Romero, Lucio Nitsch, Philippe Bouhanna, Livia Marcato,[...]. Prenat Diagn 2012
37
8

Prenatal Diagnosis of BACs-on-Beads Assay in 3647 Cases of Amniotic Fluid Cells.
Chunyan Li, Biliang Chen, Jiao Zheng, Lu Cheng, Tingting Song, Fenfen Guo, Hui Xu, Feng Yan, Ying Xu, Yu Li,[...]. Reprod Sci 2019
12
16


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.