A citation-based method for searching scientific literature

F Qiao, Y Wang, C Zhang, R Zhou, Y Wu, C Wang, L Meng, P Mao, Q Cheng, C Luo, P Hu, Z Xu. Ultrasound Obstet Gynecol 2021
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Genetic evaluation and counseling of couples with recurrent miscarriage: recommendations of the National Society of Genetic Counselors.
Mercy Y Laurino, Robin L Bennett, Devki S Saraiya, Lisa Baumeister, Debra Lochner Doyle, Kathleen Leppig, Barbara Pettersen, Robert Resta, Larry Shields, Stefanie Uhrich,[...]. J Genet Couns 2005
27
50

Diagnosis of miscarriages by molecular karyotyping: benefits and pitfalls.
Caroline Robberecht, Vicky Schuddinck, Jean-Pierre Fryns, Joris Robert Vermeesch. Genet Med 2009
63
50

Association between fetal chromosomal abnormalities and the frequency of spontaneous abortions.
Lan Yang, Tao Tao, Xin Zhao, Hehua Tao, Jingna Su, Ye Shen, Ye Tang, Fangbo Qian, Jianping Xiao. Exp Ther Med 2020
3
50

Recurrent pregnancy loss: current perspectives.
Hady El Hachem, Vincent Crepaux, Pascale May-Panloup, Philippe Descamps, Guillaume Legendre, Pierre-Emmanuel Bouet. Int J Womens Health 2017
105
50

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
384
50

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
53
50

Prognosis for live birth in women with recurrent miscarriage: what is the best measure of success?
Marie Lund, Mads Kamper-Jørgensen, Henriette Svarre Nielsen, Øjvind Lidegaard, Anne-Marie Nybo Andersen, Ole Bjarne Christiansen. Obstet Gynecol 2012
57
50

Predictors of pregnancy success in repeated miscarriage.
M N Cauchi, R Pepperell, M Kloss, D Lim. Am J Reprod Immunol 1991
13
50

Comparative Cytogenetic Analysis of Spontaneous Abortions in Recurrent and Sporadic Pregnancy Losses.
Tatiana V Nikitina, Elena A Sazhenova, Ekaterina N Tolmacheva, Natalia N Sukhanova, Anna A Kashevarova, Nikolay A Skryabin, Stanislav A Vasilyev, Tatiana N Nemtseva, Sergey Y Yuriev, Igor N Lebedev. Biomed Hub 2016
8
50

Etiology of recurrent pregnancy loss in women over the age of 35 years.
Kerri Marquard, Lynn M Westphal, Amin A Milki, Ruth B Lathi. Fertil Steril 2010
65
50

Frequency of abnormal karyotypes among abortuses from women with and without a history of recurrent spontaneous abortion.
J J Stern, A D Dorfmann, A J Gutiérrez-Najar, M Cerrillo, C B Coulam. Fertil Steril 1996
121
50

Systematic analysis of copy-number variations associated with early pregnancy loss.
Y Wang, Y Li, Y Chen, R Zhou, Z Sang, L Meng, J Tan, F Qiao, Q Bao, D Luo,[...]. Ultrasound Obstet Gynecol 2020
16
50

Recurrent Pregnancy Loss: Generally Accepted Causes and Their Management.
Jennifer Kaiser, D Ware Branch. Clin Obstet Gynecol 2016
12
50

Maternal age and fetal loss: population based register linkage study.
A M Nybo Andersen, J Wohlfahrt, P Christens, J Olsen, M Melbye. BMJ 2000
802
50

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
88
50

Evidence-based guidelines for the investigation and medical treatment of recurrent miscarriage.
Eric Jauniaux, Roy G Farquharson, Ole B Christiansen, Niek Exalto. Hum Reprod 2006
293
50


An update in recurrent spontaneous abortion.
Manoj Kumar Pandey, Reena Rani, Suraksha Agrawal. Arch Gynecol Obstet 2005
116
50

Frequency of recurrent spontaneous abortion and its influence on further marital relationship and illness: the Okazaki Cohort Study in Japan.
Mayumi Sugiura-Ogasawara, Sadao Suzuki, Yasuhiko Ozaki, Kinue Katano, Nobuhiro Suzumori, Tamao Kitaori. J Obstet Gynaecol Res 2013
26
50

Cytogenetic testing of anembryonic pregnancies compared to embryonic missed abortions.
Ruth B Lathi, Sara D Mark, Lynn M Westphal, Amin A Milki. J Assist Reprod Genet 2007
24
50

Genetics of early miscarriage.
Merel M J van den Berg, Merel C van Maarle, Madelon van Wely, Mariëtte Goddijn. Biochim Biophys Acta 2012
122
50

Embryonic karyotype of abortuses in relation to the number of previous miscarriages.
M Ogasawara, K Aoki, S Okada, K Suzumori. Fertil Steril 2000
277
50


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
29
50

Recurrent fetal aneuploidy and recurrent miscarriage.
Amy E Sullivan, Robert M Silver, D Yvette LaCoursiere, T Flint Porter, D Ware Branch. Obstet Gynecol 2004
88
50


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
19
50

New insights into mechanisms behind miscarriage.
Elisabeth Clare Larsen, Ole Bjarne Christiansen, Astrid Marie Kolte, Nick Macklon. BMC Med 2013
210
50

Genetic aspects of miscarriage.
M Goddijn, N J Leschot. Baillieres Best Pract Res Clin Obstet Gynaecol 2000
137
50

Recurrent miscarriage: pathophysiology and outcome.
Belinda Carrington, Gavin Sacks, Lesley Regan. Curr Opin Obstet Gynecol 2005
109
50


Lessons from exome sequencing in prenatally diagnosed heart defects: A basis for prenatal testing.
Dominik S Westphal, Gloria S Leszinski, Esther Rieger-Fackeldey, Elisabeth Graf, Gregor Weirich, Thomas Meitinger, Eva Ostermayer, Renate Oberhoffer, Matias Wagner. Clin Genet 2019
13
50

Clinical utility of exome sequencing in the prenatal diagnosis of congenital anomalies: A Review.
Fionnuala Mone, Elizabeth Quinlan-Jones, Mark D Kilby. Eur J Obstet Gynecol Reprod Biol 2018
11
50

The prevalence of genetic diagnoses in fetuses with severe congenital heart defects.
Amber E L van Nisselrooij, Malou A Lugthart, Sally-Ann Clur, Ingeborg H Linskens, Eva Pajkrt, Lukas A Rammeloo, Lieke Rozendaal, Nico A Blom, Jan M M van Lith, Alida C Knegt,[...]. Genet Med 2020
14
50

Exome sequencing in the assessment of congenital malformations in the fetus and neonate.
Fionnuala Mone, Elizabeth Quinlan-Jones, Andrew K Ewer, Mark D Kilby. Arch Dis Child Fetal Neonatal Ed 2019
9
50

Reproductive genetic counseling challenges associated with diagnostic exome sequencing in a large academic private reproductive genetic counseling practice.
Lauren E Westerfield, Samantha R Stover, Veena S Mathur, Salma A Nassef, Tiffiney G Carter, Yaping Yang, Christine M Eng, Ignatia B Van den Veyver. Prenat Diagn 2015
31
50

Next generation sequencing--implications for clinical practice.
Eleanor Raffan, Robert K Semple. Br Med Bull 2011
33
50

Diagnostic power and clinical impact of exome sequencing in a cohort of 500 patients with rare diseases.
Caio Robledo D'Angioli Costa Quaio, Caroline Monaco Moreira, Gil Monteiro Novo-Filho, Patricia Rossi Sacramento-Bobotis, Michele Groenner Penna, Sandro Felix Perazzio, Aurelio Pimenta Dutra, Rafael Alves da Silva, Monize Nakamoto Provisor Santos, Vanessa Yurie Nozaki de Arruda,[...]. Am J Med Genet C Semin Med Genet 2020
5
50

Prenatal whole exome sequencing: the views of clinicians, scientists, genetic counsellors and patient representatives.
Elizabeth Quinlan-Jones, Mark D Kilby, Sheila Greenfield, Michael Parker, Dominic McMullan, Matthew E Hurles, Sarah C Hillman. Prenat Diagn 2016
27
50

Preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P) 2015: elaboration and explanation.
Larissa Shamseer, David Moher, Mike Clarke, Davina Ghersi, Alessandro Liberati, Mark Petticrew, Paul Shekelle, Lesley A Stewart. BMJ 2015
50

Novel and recurrent variants identified in fetuses with central nervous system abnormalities by trios-medical exome sequencing.
Hu Tan, Yinong Xie, Fei Chen, Min Chen, Li Yu, Dunjin Chen, Jingsi Chen. Clin Chim Acta 2020
2
50

New genetic testing in prenatal diagnosis.
Natalia Babkina, John M Graham. Semin Fetal Neonatal Med 2014
15
50

Prenatal diagnosis of skeletal dysplasias using whole exome sequencing in China.
Jia Tang, Chenglong Zhou, Haihong Shi, Yuying Mo, Weilan Tan, Tielan Sun, Jinling Zhu, Qing Li, Hui Li, Yuping Li,[...]. Clin Chim Acta 2020
6
50

Simultaneous Detection of CNVs and SNVs Improves the Diagnostic Yield of Fetuses with Ultrasound Anomalies and Normal Karyotypes.
Qingwei Qi, Yulin Jiang, Xiya Zhou, Hua Meng, Na Hao, Jiazhen Chang, Junjie Bai, Chunli Wang, Mingming Wang, Jiangshan Guo,[...]. Genes (Basel) 2020
3
50

Exploring the Issues Surrounding Clinical Exome Sequencing in the Prenatal Setting.
Swetha Narayanan, Bruce Blumberg, Marla L Clayman, Vivian Pan, Catherine Wicklund. J Genet Couns 2018
8
50

Genomic medicine for undiagnosed diseases.
Anastasia L Wise, Teri A Manolio, George A Mensah, Josh F Peterson, Dan M Roden, Cecelia Tamburro, Marc S Williams, Eric D Green. Lancet 2019
30
50

Targeted gene sequencing and whole-exome sequencing in autopsied fetuses with prenatally diagnosed kidney anomalies.
M Rasmussen, L Sunde, M L Nielsen, M Ramsing, A Petersen, T D Hjortshøj, T E Olsen, A Tabor, J M Hertz, I Johnsen,[...]. Clin Genet 2018
24
50

Actions and Uncertainty: How Prenatally Diagnosed Variants of Uncertain Significance Become Actionable.
Allison Werner-Lin, Judith L M Mccoyd, Barbara A Bernhardt. Hastings Cent Rep 2019
7
50

Whole-exome sequencing reanalysis at 12 months boosts diagnosis and is cost-effective when applied early in Mendelian disorders.
Lisa J Ewans, Deborah Schofield, Rupendra Shrestha, Ying Zhu, Velimir Gayevskiy, Kevin Ying, Corrina Walsh, Eric Lee, Edwin P Kirk, Alison Colley,[...]. Genet Med 2018
59
50

Fetal Exome Sequencing on the Horizon.
Karen Wou, Isabelle DeBie, June Carroll, Jo-Ann Brock, R Douglas Wilson. J Obstet Gynaecol Can 2019
5
50


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.