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: 61







List of co-cited articles
303 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
94
36


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
37
43

Genetics of early miscarriage.
Merel M J van den Berg, Merel C van Maarle, Madelon van Wely, Mariëtte Goddijn. Biochim Biophys Acta 2012
117
21

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
138
21


Recurrent miscarriage.
Raj Rai, Lesley Regan. Lancet 2006
732
19



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
87
18

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
140
18

Embryonic karyotype of abortuses in relation to the number of previous miscarriages.
M Ogasawara, K Aoki, S Okada, K Suzumori. Fertil Steril 2000
274
18

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
524
18


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
50
20

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

Diagnosis of miscarriages by molecular karyotyping: benefits and pitfalls.
Caroline Robberecht, Vicky Schuddinck, Jean-Pierre Fryns, Joris Robert Vermeesch. Genet Med 2009
63
14

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
52
17

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
657
13

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
24
33

New insights into mechanisms behind miscarriage.
Elisabeth Clare Larsen, Ole Bjarne Christiansen, Astrid Marie Kolte, Nick Macklon. BMC Med 2013
206
13

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
74
13

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

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
13
53

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

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
30
20

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

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
105
9

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
65
9

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
82
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
139
9

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
9

Genetic aspects of miscarriage.
M Goddijn, N J Leschot. Baillieres Best Pract Res Clin Obstet Gynaecol 2000
136
9

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
9

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
38
15

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
27
22

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
11
54

ESHRE guideline: recurrent pregnancy loss.
Ruth Bender Atik, Ole Bjarne Christiansen, Janine Elson, Astrid Marie Kolte, Sheena Lewis, Saskia Middeldorp, Willianne Nelen, Braulio Peramo, Siobhan Quenby, Nathalie Vermeulen,[...]. Hum Reprod Open 2018
158
9

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



Cost-effectiveness of cytogenetic evaluation of products of conception in the patient with a second pregnancy loss.
Nastaran Foyouzi, Marcelle I Cedars, Heather G Huddleston. Fertil Steril 2012
33
15

Abnormalities in spontaneous abortions detected by G-banding and chromosomal microarray analysis (CMA) at a national reference laboratory.
Boris T Wang, Thomas P Chong, Fatih Z Boyar, Kimberly A Kopita, Leslie P Ross, Mohamed M El-Naggar, Trilochan Sahoo, Jia-Chi Wang, Morteza Hemmat, Mary H Haddadin,[...]. Mol Cytogenet 2014
21
23

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
198
8

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
46
10

The nature of aneuploidy with increasing age of the female partner: a review of 15,169 consecutive trophectoderm biopsies evaluated with comprehensive chromosomal screening.
Jason M Franasiak, Eric J Forman, Kathleen H Hong, Marie D Werner, Kathleen M Upham, Nathan R Treff, Richard T Scott. Fertil Steril 2014
367
8

Abnormal embryonic karyotype is the most frequent cause of recurrent miscarriage.
Mayumi Sugiura-Ogasawara, Yasuhiko Ozaki, Kinue Katano, Nobuhiro Suzumori, Tamao Kitaori, Eita Mizutani. Hum Reprod 2012
85
8


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.