A citation-based method for searching scientific literature

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, Carlos W Benito, Mandolin S Ziadie, Karine Hovanes. Genet Med 2017
Times Cited: 55







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



Times Cited
  Times     Co-cited
Similarity


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
87
34


Clinical application of SNP array analysis in first-trimester pregnancy loss: a prospective study.
Y Wang, Q Cheng, L Meng, C Luo, H Hu, J Zhang, J Cheng, T Xu, T Jiang, D Liang,[...]. Clin Genet 2017
36
44


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
136
21


Recurrent miscarriage.
Raj Rai, Lesley Regan. Lancet 2006
706
20

Genetics of early miscarriage.
Merel M J van den Berg, Merel C van Maarle, Madelon van Wely, Mariëtte Goddijn. Biochim Biophys Acta 2012
110
20

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
40

Karyotype versus microarray testing for genetic abnormalities after stillbirth.
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,[...]. N Engl J Med 2012
138
20


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
504
20

Cytogenetic diagnosis of "normal 46,XX" karyotypes in spontaneous abortions frequently may be misleading.
K A Bell, P G Van Deerlin, B R Haddad, R F Feinberg. Fertil Steril 1999
85
18

Embryonic karyotype of abortuses in relation to the number of previous miscarriages.
M Ogasawara, K Aoki, S Okada, K Suzumori. Fertil Steril 2000
268
18

Spontaneous abortion and recurrent miscarriage: A comparison of cytogenetic diagnosis in 250 cases.
Tae Yeong Choi, Hye Min Lee, Won Kyoung Park, So Yeong Jeong, Hwa Sook Moon. Obstet Gynecol Sci 2014
37
24

Genetic analysis of first-trimester miscarriages with a combination of cytogenetic karyotyping, microsatellite genotyping and arrayCGH.
Y-X Zhang, Y-P Zhang, Y Gu, F-J Guan, S-L Li, J-S Xie, Y Shen, B-L Wu, W Ju, E C Jenkins,[...]. Clin Genet 2009
52
17

Reliability of 46,XX results on miscarriage specimens: a review of 1,222 first-trimester miscarriage specimens.
Ruth B Lathi, Stephanie L F Gustin, Jennifer Keller, Melissa K Maisenbacher, Styrmir Sigurjonsson, Rosina Tao, Zach Demko. Fertil Steril 2014
48
18


Chromosomal copy number analysis on chorionic villus samples from early spontaneous miscarriages by high throughput genetic technology.
Jiandong Shen, Wei Wu, Chao Gao, Humphrey Ochin, Dianyun Qu, Jiazi Xie, Li Gao, Yadong Zhou, Yugui Cui, Jiayin Liu. Mol Cytogenet 2016
22
36

The effect of maternal age on chromosomal anomaly rate and spectrum in recurrent miscarriage.
Maribel Grande, Antoni Borrell, Raul Garcia-Posada, Virginia Borobio, Miriam Muñoz, Montserrat Creus, Anna Soler, Aurora Sanchez, Juan Balasch. Hum Reprod 2012
48
16

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
630
12

Improved assay performance of single nucleotide polymorphism array over conventional karyotyping in analyzing products of conception.
Shao-Bin Lin, Ying-Jun Xie, Zheng Chen, Yi Zhou, Jian-Zhu Wu, Zhi-Qiang Zhang, Shan-Shan Shi, Bao-Jiang Chen, Qun Fang. J Chin Med Assoc 2015
17
41

New insights into mechanisms behind miscarriage.
Elisabeth Clare Larsen, Ole Bjarne Christiansen, Astrid Marie Kolte, Nick Macklon. BMC Med 2013
195
12

Diagnosis of miscarriages by molecular karyotyping: benefits and pitfalls.
Caroline Robberecht, Vicky Schuddinck, Jean-Pierre Fryns, Joris Robert Vermeesch. Genet Med 2009
61
12

Low-pass whole-genome sequencing in clinical cytogenetics: a validated approach.
Zirui Dong, Jun Zhang, Ping Hu, Haixiao Chen, Jinjin Xu, Qi Tian, Lu Meng, Yanchou Ye, Jun Wang, Meiyan Zhang,[...]. Genet Med 2016
67
12

Array-based comparative genomic hybridization is more informative than conventional karyotyping and fluorescence in situ hybridization in the analysis of first-trimester spontaneous abortion.
Jinsong Gao, Congcong Liu, Fengxia Yao, Na Hao, Jing Zhou, Qian Zhou, Liang Zhang, Xinyan Liu, Xuming Bian, Juntao Liu. Mol Cytogenet 2012
31
19

First-trimester euploid miscarriages analysed by array-CGH.
Chiara Donatella Viaggi, S Cavani, M Malacarne, F Floriddia, G Zerega, C Baldo, M Mogni, M Castagnetta, G Piombo, D A Coviello,[...]. J Appl Genet 2013
30
20

Single-Nucleotide Polymorphism-Microarray Ploidy Analysis of Paraffin-Embedded Products of Conception in Recurrent Pregnancy Loss Evaluations.
Bat-Sheva L Maslow, Tara Budinetz, Carolina Sueldo, Erica Anspach, Lawrence Engmann, Claudio Benadiva, John C Nulsen. Obstet Gynecol 2015
12
50

Identification of copy number variants in miscarriages from couples with idiopathic recurrent pregnancy loss.
E Rajcan-Separovic, D Diego-Alvarez, W P Robinson, C Tyson, Y Qiao, C Harvard, C Fawcett, D Kalousek, T Philipp, M J Somerville,[...]. Hum Reprod 2010
64
10

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
10

Recurrent fetal aneuploidy and recurrent miscarriage.
Amy E Sullivan, Robert M Silver, D Yvette LaCoursiere, T Flint Porter, D Ware Branch. Obstet Gynecol 2004
84
10

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
36
16

Potential genetic causes of miscarriage in euploid pregnancies: a systematic review.
Emily Colley, Susan Hamilton, Paul Smith, Neil V Morgan, Arri Coomarasamy, Stephanie Allen. Hum Reprod Update 2019
19
31

Informatics enhanced SNP microarray analysis of 30 miscarriage samples compared to routine cytogenetics.
Ruth B Lathi, Jamie A M Massie, Megan Loring, Zachary P Demko, David Johnson, Styrmir Sigurjonsson, George Gemelos, Matthew Rabinowitz. PLoS One 2012
28
17

Array comparative genomic hybridization for genetic evaluation of fetal loss between 10 and 20 weeks of gestation.
Jennifer E Warren, David K Turok, Teresa M Maxwell, Arthur R Brothman, Robert M Silver. Obstet Gynecol 2009
33
15

Analysis of tissue from products of conception and perinatal losses using QF-PCR and microarray: A three-year retrospective study resulting in an efficient protocol.
K Wou, Y Hyun, D Chitayat, M Vlasschaert, K Chong, S Wasim, S Keating, P Shannon, E Kolomietz. Eur J Med Genet 2016
9
55

Cytogenetic analysis of 750 spontaneous abortions with the direct-preparation method of chorionic villi and its implications for studying genetic causes of pregnancy wastage.
B Eiben, I Bartels, S Bähr-Porsch, S Borgmann, G Gatz, G Gellert, R Goebel, W Hammans, M Hentemann, R Osmers. Am J Hum Genet 1990
196
9

Comparative genomic hybridization in combination with flow cytometry improves results of cytogenetic analysis of spontaneous abortions.
B Lomax, S Tang, E Separovic, D Phillips, E Hillard, T Thomson, D K Kalousek. Am J Hum Genet 2000
104
9

Overview of Chromosome Abnormalities in First Trimester Miscarriages: A Series of 1,011 Consecutive Chorionic Villi Sample Karyotypes.
Anna Soler, Carme Morales, Irene Mademont-Soler, Ester Margarit, Antoni Borrell, Virginia Borobio, Miriam Muñoz, Aurora Sánchez. Cytogenet Genome Res 2017
41
12

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
79
9

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
135
9

Genetic aspects of miscarriage.
M Goddijn, N J Leschot. Baillieres Best Pract Res Clin Obstet Gynaecol 2000
132
9

Maternal age and fetal loss: population based register linkage study.
A M Nybo Andersen, J Wohlfahrt, P Christens, J Olsen, M Melbye. BMJ 2000
778
9

Added value of chromosomal microarray analysis over karyotyping in early pregnancy loss: systematic review and meta-analysis.
M Pauta, M Grande, L Rodriguez-Revenga, E Kolomietz, A Borrell. Ultrasound Obstet Gynecol 2018
17
29

Maternal age, history of miscarriage, and embryonic/fetal size are associated with cytogenetic results of spontaneous early miscarriages.
Nobuaki Ozawa, Kohei Ogawa, Aiko Sasaki, Mari Mitsui, Seiji Wada, Haruhiko Sago. J Assist Reprod Genet 2019
9
55

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

Diagnostic utility of novel combined arrays for genome-wide simultaneous detection of aneuploidy and uniparental isodisomy in losses of pregnancy.
Stefanie Bug, Beate Solfrank, Felizitas Schmitz, Jana Pricelius, Mona Stecher, Andrew Craig, Marc Botcherby, Claudia Nevinny-Stickel-Hinzpeter. Mol Cytogenet 2014
18
22

Double trisomy in spontaneous miscarriages: cytogenetic and molecular approach.
Dan Diego-Alvarez, Carmen Ramos-Corrales, Maria Garcia-Hoyos, Ana Bustamante-Aragones, Diego Cantalapiedra, Joaquin Diaz-Recasens, Elena Vallespin-Garcia, Carmen Ayuso, Isabel Lorda-Sanchez. Hum Reprod 2006
41
9

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
29
13



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.