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


Differentiation of genetic abnormalities in early pregnancy loss.
S T Romero, K B Geiersbach, C N Paxton, N C Rose, E F Schisterman, D W Branch, R M Silver. Ultrasound Obstet Gynecol 2015
30
13

Recurrent fetal aneuploidy and recurrent miscarriage.
Amy E Sullivan, Robert M Silver, D Yvette LaCoursiere, T Flint Porter, D Ware Branch. Obstet Gynecol 2004
87
4


Clinical validation of a noninvasive prenatal test for genomewide detection of fetal copy number variants.
Roy B Lefkowitz, John A Tynan, Tong Liu, Yijin Wu, Amin R Mazloom, Eyad Almasri, Grant Hogg, Vach Angkachatchai, Chen Zhao, Daniel S Grosu,[...]. Am J Obstet Gynecol 2016
89
4

Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes.
Ronald J Wapner, Joshua E Babiarz, Brynn Levy, Melissa Stosic, Bernhard Zimmermann, Styrmir Sigurjonsson, Nicholas Wayham, Allison Ryan, Milena Banjevic, Phil Lacroute,[...]. Am J Obstet Gynecol 2015
175
4

Exome sequencing positively identified relevant alterations in more than half of cases with an indication of prenatal ultrasound anomalies.
Christina L Alamillo, Zöe Powis, Kelly Farwell, Layla Shahmirzadi, Elaine C Weltmer, John Turocy, Thomas Lowe, Christine Kobelka, Emily Chen, Donald Basel,[...]. Prenat Diagn 2015
56
7

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet Med 2013
4

Women's experiences receiving abnormal prenatal chromosomal microarray testing results.
Barbara A Bernhardt, Danielle Soucier, Karen Hanson, Melissa S Savage, Laird Jackson, Ronald J Wapner. Genet Med 2013
132
4

Tissue sampling technique affects accuracy of karyotype from missed abortions.
Ruth B Lathi, Amin A Milki. J Assist Reprod Genet 2002
44
9

A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population.
Lorenzo D Botto, Kristin May, Paul M Fernhoff, Adolfo Correa, Karlene Coleman, Sonja A Rasmussen, Robert K Merritt, Leslie A O'Leary, Lee-Yang Wong, E Marsha Elixson,[...]. Pediatrics 2003
411
4


Human cytomegalovirus infection is detected frequently in stillbirths and is associated with fetal thrombotic vasculopathy.
Jenna M Iwasenko, Jonathan Howard, Susan Arbuckle, Nicole Graf, Beverley Hall, Maria E Craig, William D Rawlinson. J Infect Dis 2011
71
5

Post-mortem MRI versus conventional autopsy in fetuses and children: a prospective validation study.
Sudhin Thayyil, Neil J Sebire, Lyn S Chitty, Angie Wade, Wk Chong, Oystein Olsen, Roxana S Gunny, Amaka C Offiah, Catherine M Owens, Dawn E Saunders,[...]. Lancet 2013
160
4

Minimally invasive perinatal autopsies using magnetic resonance imaging and endoscopic postmortem examination ("keyhole autopsy"): feasibility and initial experience.
Neil J Sebire, Martin A Weber, Sudhin Thayyil, Imran Mushtaq, Andrew Taylor, Lyn S Chitty. J Matern Fetal Neonatal Med 2012
61
6

Radiographic evaluation of stillbirth: what does it contribute?
Erica Swenson, Lynn Schema, Elizabeth McPherson. Am J Med Genet A 2014
5
80

Diagnostic evaluation of intrauterine fetal deaths in Stockholm 1998-99.
Karin Petersson, Katarina Bremme, Roger Bottinga, Alexandra Hofsjö, Ingela Hulthén-Varli, Marius Kublickas, Margareta Norman, Nikos Papadogiannakis, Kjell Wånggren, Kerstin Wolff. Acta Obstet Gynecol Scand 2002
62
6

High-resolution chromosomal microarrays in prenatal diagnosis significantly increase diagnostic power.
Beatrice Oneda, Rosa Baldinger, Regina Reissmann, Irina Reshetnikova, Pavel Krejci, Rahim Masood, Nicole Ochsenbein-Kölble, Deborah Bartholdi, Katharina Steindl, Denise Morotti,[...]. Prenat Diagn 2014
29
13



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
807
4

Analysis of protein-coding genetic variation in 60,706 humans.
Monkol Lek, Konrad J Karczewski, Eric V Minikel, Kaitlin E Samocha, Eric Banks, Timothy Fennell, Anne H O'Donnell-Luria, James S Ware, Andrew J Hill, Beryl B Cummings,[...]. Nature 2016
4

Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units.
Carol Jean Saunders, Neil Andrew Miller, Sarah Elizabeth Soden, Darrell Lee Dinwiddie, Aaron Noll, Noor Abu Alnadi, Nevene Andraws, Melanie LeAnn Patterson, Lisa Ann Krivohlavek, Joel Fellis,[...]. Sci Transl Med 2012
371
4

Recurrence of stillbirth and second trimester pregnancy loss.
Elizabeth McPherson. Am J Med Genet A 2016
12
33

Interventions for investigating and identifying the causes of stillbirth.
Aleena M Wojcieszek, Emily Shepherd, Philippa Middleton, Glenn Gardener, David A Ellwood, Elizabeth M McClure, Katherine J Gold, Teck Yee Khong, Robert M Silver, Jan Jaap Hm Erwich,[...]. Cochrane Database Syst Rev 2018
14
28

Making stillbirths visible: a systematic review of globally reported causes of stillbirth.
H E Reinebrant, S H Leisher, M Coory, S Henry, A M Wojcieszek, G Gardener, R Lourie, D Ellwood, Z Teoh, E Allanson,[...]. BJOG 2018
67
5

Characterization of chromosomal abnormalities in pregnancy losses reveals critical genes and loci for human early development.
Yiyun Chen, Justin Bartanus, Desheng Liang, Hongmin Zhu, Amy M Breman, Janice L Smith, Hua Wang, Zhilin Ren, Ankita Patel, Pawel Stankiewicz,[...]. Hum Mutat 2017
14
28

Microarrays in prenatal diagnosis.
Beatrice Oneda, Anita Rauch. Best Pract Res Clin Obstet Gynaecol 2017
21
19

Comparison of cytogenetics and molecular karyotyping for chromosome testing of miscarriage specimens.
Meera Sridhar Shah, Cengiz Cinnioglu, Melissa Maisenbacher, Ioanna Comstock, Jonathan Kort, Ruth Bunker Lathi. Fertil Steril 2017
24
16


Recurrent miscarriage.
Raj Rai, Lesley Regan. Lancet 2006
732
4


Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorder.
Elizabeth A Normand, Alicia Braxton, Salma Nassef, Patricia A Ward, Francesco Vetrini, Weimin He, Vipulkumar Patel, Chunjing Qu, Lauren E Westerfield, Samantha Stover,[...]. Genome Med 2018
48
8

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
28
14

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
107
3

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
3

Amniocentesis or chorionic villus sampling in multiple gestations? Experience with 500 cases.
C van den Berg, A P Braat, D Van Opstal, D J Halley, W J Kleijer, N S den Hollander, H Brandenburg, L Pijpers, F J Los. Prenat Diagn 1999
29
10

Chorionic villus sampling and transverse digital deficiencies: evidence for anatomic and gestational-age specificity of the digital deficiencies in two studies.
L D Botto, R S Olney, P Mastroiacovo, M J Khoury, C A Moore, C J Alo, P Costa, L D Edmonds, T J Flood, J A Harris,[...]. Am J Med Genet 1996
18
16

Pregnancy loss rate after mid-trimester amniocentesis in twin pregnancies.
Alison G Cahill, George A Macones, David M Stamilio, Jeffrey M Dicke, James P Crane, Anthony O Odibo. Am J Obstet Gynecol 2009
34
8


Mid-trimester genetic amniocentesis in twin pregnancy and the risk of fetal loss.
Mélanie Millaire, Emmanuel Bujold, Anne-Maude Morency, Robert J Gauthier. J Obstet Gynaecol Can 2006
32
9

Detection of hepatitis C virus RNA (HCV RNA) in amniotic fluid: a prospective study.
C Delamare, B Carbonne, N Heim, N Berkane, J C Petit, S Uzan, J D Grangé. J Hepatol 1999
49
6

Confined placental mosaicism at chorionic villous sampling: risk factors and pregnancy outcome.
Giulia Maria Baffero, Edgardo Somigliana, Francesca Crovetto, Alessio Paffoni, Nicola Persico, Silvana Guerneri, Faustina Lalatta, Roberto Fogliani, Luigi Fedele. Prenat Diagn 2012
30
10



Randomised study of risk of fetal loss related to early amniocentesis versus chorionic villus sampling.
K Sundberg, J Bang, S Smidt-Jensen, V Brocks, C Lundsteen, J Parner, N Keiding, J Philip. Lancet 1997
110
3

Risk of vertical transmission of hepatitis B after amniocentesis in HBs antigen-positive mothers.
Wei Yi, Calvin Q Pan, Jianzhen Hao, Yuhong Hu, Min Liu, Li Li, Dongzhu Liang. J Hepatol 2014
55
5






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.