A citation-based method for searching scientific literature

Uma M Reddy, Grier P Page, George R Saade, Robert M Silver, Vanessa R Thorsten, Corette B Parker, Halit Pinar, Marian Willinger, Barbara J Stoll, Josefine Heim-Hall, Michael W Varner, Robert L Goldenberg, Radek Bukowski, Ronald J Wapner, Carolyn D Drews-Botsch, Barbara M O'Brien, Donald J Dudley, Brynn Levy. N Engl J Med 2012
Times Cited: 140







List of co-cited articles
862 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
646
47

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


Cytogenetic analysis after evaluation of 750 fetal deaths: proposal for diagnostic workup.
Fleurisca J Korteweg, Katelijne Bouman, Jan Jaap H M Erwich, Albertus Timmer, Nic J G M Veeger, Joke M Ravisé, Thomas H Nijman, Jozien P Holm. Obstet Gynecol 2008
59
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
154
15

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
516
14

Genomic imbalance in products of conception: single-nucleotide polymorphism chromosomal microarray analysis.
Brynn Levy, Styrmir Sigurjonsson, Barbara Pettersen, Melissa K Maisenbacher, Megan P Hall, Zachary Demko, Ruth B Lathi, Rosina Tao, Vimla Aggarwal, Matthew Rabinowitz. Obstet Gynecol 2014
93
15

Evaluation of 1025 fetal deaths: proposed diagnostic workup.
Fleurisca J Korteweg, Jan Jaap H M Erwich, Albertus Timmer, Jan van der Meer, Joke M Ravisé, Nic J G M Veeger, Jozien P Holm. Am J Obstet Gynecol 2012
59
22


Diagnostic Tests for Evaluation of Stillbirth: Results From the Stillbirth Collaborative Research Network.
Jessica M Page, Lauren Christiansen-Lindquist, Vanessa Thorsten, Corette B Parker, Uma M Reddy, Donald J Dudley, George R Saade, Donald Coustan, Carol J Rowland Hogue, Deborah Conway,[...]. Obstet Gynecol 2017
41
29

Clinical whole-exome sequencing for the diagnosis of mendelian disorders.
Yaping Yang, Donna M Muzny, Jeffrey G Reid, Matthew N Bainbridge, Alecia Willis, Patricia A Ward, Alicia Braxton, Joke Beuten, Fan Xia, Zhiyv Niu,[...]. N Engl J Med 2013
11

Incidence and spectrum of chromosome abnormalities in spontaneous abortions: new insights from a 12-year study.
Joshua Menasha, Brynn Levy, Kurt Hirschhorn, Nataline B Kardon. Genet Med 2005
137
11


Comprehensive genetic analysis of pregnancy loss by chromosomal microarrays: outcomes, benefits, and challenges.
Trilochan Sahoo, Natasa Dzidic, Michelle N Strecker, Sara Commander, Mary K Travis, Charles Doherty, R Weslie Tyson, Arturo E Mendoza, Mary Stephenson, Craig A Dise,[...]. Genet Med 2017
61
18

Major risk factors for stillbirth in high-income countries: a systematic review and meta-analysis.
Vicki Flenady, Laura Koopmans, Philippa Middleton, J Frederik Frøen, Gordon C Smith, Kristen Gibbons, Michael Coory, Adrienne Gordon, David Ellwood, Harold David McIntyre,[...]. Lancet 2011
637
10

Diagnostic utility of microarray testing in pregnancy loss.
J A Rosenfeld, M E Tucker, L F Escobar, N J Neill, B S Torchia, L D McDaniel, R A Schultz, K Chong, D Chitayat. Ultrasound Obstet Gynecol 2015
27
37

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
10

The use of chromosomal microarray for prenatal diagnosis.
Lorraine Dugoff, Mary E Norton, Jeffrey A Kuller. Am J Obstet Gynecol 2016
62
16



Detection rates of clinically significant genomic alterations by microarray analysis for specific anomalies detected by ultrasound.
Lisa G Shaffer, Jill A Rosenfeld, Mindy P Dabell, Justine Coppinger, Anne M Bandholz, Jay W Ellison, J Britt Ravnan, Beth S Torchia, Blake C Ballif, Allan J Fisher. Prenat Diagn 2012
138
9



The role of DNA microarrays in the evaluation of fetal death.
Uma M Reddy, Grier P Page, George R Saade. Prenat Diagn 2012
20
40


Long QT syndrome-associated mutations in intrauterine fetal death.
Lia Crotti, David J Tester, Wendy M White, Daniel C Bartos, Roberto Insolia, Alessandra Besana, Jennifer D Kunic, Melissa L Will, Ellyn J Velasco, Jennifer J Bair,[...]. JAMA 2013
87
9

Exome sequencing for prenatal diagnosis of fetuses with sonographic abnormalities.
Suzanne Drury, Hywel Williams, Natalie Trump, Christopher Boustred, Nicholas Lench, Richard H Scott, Lyn S Chitty. Prenat Diagn 2015
111
8

Stillbirth evaluation: a stepwise assessment of placental pathology and autopsy.
Emily S Miller, Lucy Minturn, Rebecca Linn, Debra E Weese-Mayer, Linda M Ernst. Am J Obstet Gynecol 2016
21
38

The stillbirth collaborative research network postmortem examination protocol.
Halit Pinar, Matthew A Koch, Hal Hawkins, Josefine Heim-Hall, Carlos R Abramowsky, Vanessa R Thorsten, Marshall W Carpenter, Hong Holly Zhou, Uma M Reddy. Am J Perinatol 2012
30
26

Molecular autopsy in maternal-fetal medicine.
Hanan E Shamseldin, Wesam Kurdi, Fatima Almusafri, Maha Alnemer, Alya Alkaff, Zeneb Babay, Amal Alhashem, Maha Tulbah, Nada Alsahan, Rubina Khan,[...]. Genet Med 2018
48
16

A new system for determining the causes of stillbirth.
Donald J Dudley, Robert Goldenberg, Deborah Conway, Robert M Silver, George R Saade, Michael W Varner, Halit Pinar, Donald Coustan, Radek Bukowski, Barbara Stoll,[...]. Obstet Gynecol 2010
72
9

Systematic review of placental pathology reported in association with stillbirth.
I Ptacek, N J Sebire, J A Man, P Brownbill, A E P Heazell. Placenta 2014
72
9

Stillbirths: rates, risk factors, and acceleration towards 2030.
Joy E Lawn, Hannah Blencowe, Peter Waiswa, Agbessi Amouzou, Colin Mathers, Dan Hogan, Vicki Flenady, J Frederik Frøen, Zeshan U Qureshi, Claire Calderwood,[...]. Lancet 2016
608
7

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
7

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
9


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

Association of copy number variants with specific ultrasonographically detected fetal anomalies.
Jennifer C Donnelly, Lawrence D Platt, Andrei Rebarber, Julia Zachary, William A Grobman, Ronald J Wapner. Obstet Gynecol 2014
81
8

Antiphospholipid antibodies in stillbirth.
Robert M Silver, Corette B Parker, Uma M Reddy, Robert Goldenberg, Donald Coustan, Donald J Dudley, George R Saade, Barbara Stoll, Matthew A Koch, Deborah Conway,[...]. Obstet Gynecol 2013
46
15

Genetics of stillbirth.
Ronald J Wapner. Clin Obstet Gynecol 2010
29
24

Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study.
Jenny Lord, Dominic J McMullan, Ruth Y Eberhardt, Gabriele Rinck, Susan J Hamilton, Elizabeth Quinlan-Jones, Elena Prigmore, Rebecca Keelagher, Sunayna K Best, Georgina K Carey,[...]. Lancet 2019
152
7

Promises, pitfalls and practicalities of prenatal whole exome sequencing.
Sunayna Best, Karen Wou, Neeta Vora, Ignatia B Van der Veyver, Ronald Wapner, Lyn S Chitty. Prenat Diagn 2018
130
7



Molecular and cytogenetic analysis in stillbirth: results from 481 consecutive cases.
Ellika Sahlin, Peter Gustavsson, Agne Liedén, Nikos Papadogiannakis, Linus Bjäreborn, Karin Pettersson, Magnus Nordenskjöld, Erik Iwarsson. Fetal Diagn Ther 2014
12
50

Incidence of early loss of pregnancy.
A J Wilcox, C R Weinberg, J F O'Connor, D D Baird, J P Schlatterer, R E Canfield, E G Armstrong, B C Nisula. N Engl J Med 1988
6


Clinical exome sequencing for genetic identification of rare Mendelian disorders.
Hane Lee, Joshua L Deignan, Naghmeh Dorrani, Samuel P Strom, Sibel Kantarci, Fabiola Quintero-Rivera, Kingshuk Das, Traci Toy, Bret Harry, Michael Yourshaw,[...]. JAMA 2014
564
6


Stillbirth and intrauterine fetal death: factors affecting determination of cause of death at autopsy.
J Man, J C Hutchinson, A E Heazell, M Ashworth, S Levine, N J Sebire. Ultrasound Obstet Gynecol 2016
34
17


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.