A citation-based method for searching scientific literature

Melissa Stosic, Brynn Levy, Ronald Wapner. Obstet Gynecol Clin North Am 2018
Times Cited: 18







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



Times Cited
  Times     Co-cited
Similarity


Prenatal diagnosis by chromosomal microarray analysis.
Brynn Levy, Ronald Wapner. Fertil Steril 2018
89
55

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
50

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
154
22

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
513
22

The use of chromosomal microarray for prenatal diagnosis.
Lorraine Dugoff, Mary E Norton, Jeffrey A Kuller. Am J Obstet Gynecol 2016
62
22

Nasal bone assessment in prenatal screening for trisomy 21.
J D Sonek, S Cicero, R Neiger, K H Nicolaides. Am J Obstet Gynecol 2006
76
16

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
16

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
16

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
16


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
320
16



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
16

Microarrays in prenatal diagnosis.
Beatrice Oneda, Anita Rauch. Best Pract Res Clin Obstet Gynaecol 2017
20
16

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
50
11


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
11

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
119
11

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
38
11


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
15
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
80
11

From karyotyping to array-CGH in prenatal diagnosis.
K D Lichtenbelt, N V A M Knoers, G H Schuring-Blom. Cytogenet Genome Res 2011
36
11

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
11

Amniocentesis and chorionic villus sampling for prenatal diagnosis.
Zarko Alfirevic, Kate Navaratnam, Faris Mujezinovic. Cochrane Database Syst Rev 2017
48
11

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
22
11


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
590
11

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
78
11


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
37
11

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
42
11

[Expert consensus on the application of low-depth whole genome sequencing in prenatal diagnosis].
Clinical Genetics Group Of Medical Genetics Branch Chinese Medical Association, Professional Committee For Prenatal Diagnosis Of Genetic Diseases Medical Genetics Branch Of Chinese Medical Association, Group Of Genetic Disease Prevention And Control Birth Defect Prevention And Control Committee Of Chinese Society Of Preventive Medicine. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 2019
3
66

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
31
11

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
74
11

Traditional banding of chromosomes for cytogenetic analysis.
Jane Bayani, Jeremy A Squire. Curr Protoc Cell Biol 2004
12
16

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
111
11

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
28
11

Estimates of penetrance for recurrent pathogenic copy-number variations.
Jill A Rosenfeld, Bradley P Coe, Evan E Eichler, Howard Cuckle, Lisa G Shaffer. Genet Med 2013
184
11


Chromosomal microarray analysis and prenatal diagnosis.
Jamie O Lo, Brian L Shaffer, Cori D Feist, Aaron B Caughey. Obstet Gynecol Surv 2014
14
14

Absent fetal nasal bone: what does it mean for the euploid fetus?
Stephanie Dukhovny, Louise Wilkins-Haug, Thomas D Shipp, Carol B Benson, Anjali J Kaimal, Rosemary Reiss. J Ultrasound Med 2013
9
11

Research electronic data capture (REDCap)--a metadata-driven methodology and workflow process for providing translational research informatics support.
Paul A Harris, Robert Taylor, Robert Thielke, Jonathon Payne, Nathaniel Gonzalez, Jose G Conde. J Biomed Inform 2009
5


Second-trimester diagnosis of cri du chat (5p-) syndrome following sonographic depiction of an absent fetal nasal bone.
David M Sherer, Pierre Eugene, Mudar Dalloul, Fady Khoury-Collado, Ehab Abdelmalek, Mila Kheyman, Joseph A Osho, Ovadia Abulafia. J Ultrasound Med 2006
14
7

ISUOG consensus statement on the impact of non-invasive prenatal testing (NIPT) on prenatal ultrasound practice.
L J Salomon, Z Alfirevic, F Audibert, K O Kagan, Dario Paladini, G Yeo, N Raine-Fenning. Ultrasound Obstet Gynecol 2014
57
5

Nasal bone length throughout gestation: normal ranges based on 3537 fetal ultrasound measurements.
J D Sonek, D McKenna, D Webb, C Croom, K Nicolaides. Ultrasound Obstet Gynecol 2003
74
5

Fetal nasal bone length in the second trimester: comparison between population groups from different ethnic origins.
Panayiota Papasozomenou, Apostolos P Athanasiadis, Menelaos Zafrakas, Eleftherios Panteris, Aristoteles Loufopoulos, Efstratios Assimakopoulos, Basil C Tarlatzis. J Perinat Med 2016
8
12

Choosing between Higher and Lower Resolution Microarrays: do Pregnant Women Have Sufficient Knowledge to Make Informed Choices Consistent with their Attitude?
S L van der Steen, E M Bunnik, M G Polak, K E M Diderich, J Verhagen-Visser, L C P Govaerts, M Joosten, M F C M Knapen, A T J I Go, D Van Opstal,[...]. J Genet Couns 2018
9
11


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.