A citation-based method for searching scientific literature

Yael Pasternak, Amihood Singer, Idit Maya, Lena Sagi-Dain, Shay Ben-Shachar, Morad Khayat, Lior Greenbaum, Michal Feingold-Zadok, Sharon Zeligson, Rivka Sukenik Halevy. J Perinat Med 2020
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity



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
50

A prognostic mRNA expression signature of four 16q24.3 genes in radio(chemo)therapy-treated head and neck squamous cell carcinoma (HNSCC).
Ludmila Wintergerst, Martin Selmansberger, Cornelius Maihoefer, Lars Schüttrumpf, Axel Walch, Christina Wilke, Adriana Pitea, Christine Woischke, Philipp Baumeister, Thomas Kirchner,[...]. Mol Oncol 2018
11
50

Inflammosome in the human endometrium: further step in the evaluation of the "maternal side".
Silvia D'Ippolito, Chiara Tersigni, Riccardo Marana, Fiorella Di Nicuolo, Raffaele Gaglione, Esther Diana Rossi, Roberta Castellani, Giovanni Scambia, Nicoletta Di Simone. Fertil Steril 2016
38
50



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
50

Noninvasive detection of fetal subchromosomal abnormalities by semiconductor sequencing of maternal plasma DNA.
Ai-hua Yin, Chun-fang Peng, Xin Zhao, Bennett A Caughey, Jie-xia Yang, Jian Liu, Wei-wei Huang, Chang Liu, Dong-hong Luo, Hai-liang Liu,[...]. Proc Natl Acad Sci U S A 2015
65
50

Comparing Serum Levels of Th17 and Treg Cytokines in Women with Unexplained Recurrent Spontaneous Abortion and Fertile Women.
Narges Roomandeh, AboTaleb Saremi, Javad Arasteh, Fatemeh Pak, Majid Mirmohammadkhani, Parviz Kokhaei, Ahad Zare. Iran J Immunol 2018
10
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
10
50

Circular binary segmentation for the analysis of array-based DNA copy number data.
Adam B Olshen, E S Venkatraman, Robert Lucito, Michael Wigler. Biostatistics 2004
50

KBG syndrome.
Dayna Morel Swols, Joseph Foster, Mustafa Tekin. Orphanet J Rare Dis 2017
20
50

Distinct pattern of Th17/Treg cells in pregnant women with a history of unexplained recurrent spontaneous abortion.
Jinfeng Qian, Na Zhang, Jing Lin, Caiyan Wang, Xinyao Pan, Lanting Chen, Dajin Li, Ling Wang. Biosci Trends 2018
36
50


Analysis of chromosome microstructures in products of conception associated with recurrent miscarriage.
Taisuke Sato, Ohsuke Migita, Hiroka Hata, Aikou Okamoto, Kenichiro Hata. Reprod Biomed Online 2019
2
50

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
50

Loss of imprinting of the human-specific imprinted gene ZNF597 causes prenatal growth retardation and dysmorphic features: implications for phenotypic overlap with Silver-Russell syndrome.
Kazuki Yamazawa, Takanobu Inoue, Yoshihiro Sakemi, Toshinori Nakashima, Hironori Yamashita, Kaduki Khono, Hideki Fujita, Keisuke Enomoto, Kazuhiko Nakabayashi, Kenichiro Hata,[...]. J Med Genet 2021
1
100

Copy number variations in neurodevelopmental disorders.
Hannah M Grayton, Cathy Fernandes, Dan Rujescu, David A Collier. Prog Neurobiol 2012
105
50

Th17 cells and related cytokines in unexplained recurrent spontaneous miscarriage at the implantation window.
Bita Saifi, Seyed Abdolrahim Rezaee, Nader Tajik, Mahmood Erfanian Ahmadpour, Mahnaz Ashrafi, Rosita Vakili, Sara SoleimaniAsl, Reza Aflatoonian, Mehdi Mehdizadeh. Reprod Biomed Online 2014
42
50

MiR-543 Promotes Proliferation and Epithelial-Mesenchymal Transition in Prostate Cancer via Targeting RKIP.
Yang Du, Xiu-Heng Liu, Heng-Cheng Zhu, Lei Wang, Jin-Zhuo Ning, Cheng-Cheng Xiao. Cell Physiol Biochem 2017
56
50

PROMISE: first-trimester progesterone therapy in women with a history of unexplained recurrent miscarriages - a randomised, double-blind, placebo-controlled, international multicentre trial and economic evaluation.
Arri Coomarasamy, Helen Williams, Ewa Truchanowicz, Paul T Seed, Rachel Small, Siobhan Quenby, Pratima Gupta, Feroza Dawood, Yvonne E Koot, Ruth Bender Atik,[...]. Health Technol Assess 2016
19
50

A modest but significant effect of CGB5 gene promoter polymorphisms in modulating the risk of recurrent miscarriage.
Kristiina Rull, Ole Bjarne Christiansen, Liina Nagirnaja, Rudi Steffensen, Tõnu Margus, Maris Laan. Fertil Steril 2013
9
50

T regulatory markers expression in unexplained recurrent spontaneous abortion.
Bita Saifi, Reza Aflatoonian, Nader Tajik, Mahmood Erfanian Ahmadpour, Rosita Vakili, Fatemehsadat Amjadi, Narges Valizade, Sanaz Ahmadi, Seyed Abdolrahim Rezaee, Mehdi Mehdizadeh. J Matern Fetal Neonatal Med 2016
11
50


Expression of GRIM-19 in unexplained recurrent spontaneous abortion and possible pathogenesis.
Yang Yang, Laiyang Cheng, Xiaohui Deng, Hongling Yu, Lan Chao. Mol Hum Reprod 2018
7
50

Diagnostic factors identified in 1020 women with two versus three or more recurrent pregnancy losses.
Carolyn R Jaslow, Judi L Carney, William H Kutteh. Fertil Steril 2010
186
50

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
69
50

mTOR Signaling pathway as a master regulator of memory CD8+ T-cells, Th17, and NK cells development and their functional properties.
Davood Rostamzadeh, Mehdi Yousefi, Mohammad Reza Haghshenas, Majid Ahmadi, Sanam Dolati, Zohreh Babaloo. J Cell Physiol 2019
17
50

Reduced Testicular Steroidogenesis and Increased Semen Oxidative Stress in Male Partners as Novel Markers of Recurrent Miscarriage.
Channa N Jayasena, Utsav K Radia, Monica Figueiredo, Larissa Franklin Revill, Anastasia Dimakopoulou, Maria Osagie, Wayne Vessey, Lesley Regan, Rajendra Rai, Waljit S Dhillo. Clin Chem 2019
11
50

Noninvasive prenatal diagnosis of common aneuploidies by semiconductor sequencing.
Can Liao, Ai-hua Yin, Chun-fang Peng, Fang Fu, Jie-xia Yang, Ru Li, Yang-yi Chen, Dong-hong Luo, Yong-ling Zhang, Yan-mei Ou,[...]. Proc Natl Acad Sci U S A 2014
82
50

KBG syndrome in two patients from Egypt.
Inas S M Sayed, Mohamed S Abdel-Hamid, Ghada M H Abdel-Salam. Am J Med Genet A 2020
2
50

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
50

Refining the Phenotype of Recurrent Rearrangements of Chromosome 16.
Serena Redaelli, Silvia Maitz, Francesca Crosti, Elena Sala, Nicoletta Villa, Luigina Spaccini, Angelo Selicorni, Miriam Rigoldi, Donatella Conconi, Leda Dalprà,[...]. Int J Mol Sci 2019
13
50

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
23
50

The sequence and analysis of duplication-rich human chromosome 16.
Joel Martin, Cliff Han, Laurie A Gordon, Astrid Terry, Shyam Prabhakar, Xinwei She, Gary Xie, Uffe Hellsten, Yee Man Chan, Michael Altherr,[...]. Nature 2004
102
50

Structural genomic variation as risk factor for idiopathic recurrent miscarriage.
Liina Nagirnaja, Priit Palta, Laura Kasak, Kristiina Rull, Ole B Christiansen, Henriette S Nielsen, Rudi Steffensen, Tõnu Esko, Maido Remm, Maris Laan. Hum Mutat 2014
16
50

Recurrent pregnancy loss: diagnostic workup after two or three pregnancy losses? A systematic review of the literature and meta-analysis.
Myrthe M van Dijk, Astrid M Kolte, Jacqueline Limpens, Emma Kirk, Siobhan Quenby, Madelon van Wely, Mariëtte Goddijn. Hum Reprod Update 2020
19
50

Novel α0-Thalassemia Deletion Identified in an Indian Infant with Hb H Disease.
Jordyn A Moore, Beverley M Pullon, Kylie M Drake, Stephen O Brennan. Hemoglobin 2020
1
100

Segmental copy number variation shapes tissue transcriptomes.
Charlotte N Henrichsen, Nicolas Vinckenbosch, Sebastian Zöllner, Evelyne Chaignat, Sylvain Pradervand, Frédéric Schütz, Manuel Ruedi, Henrik Kaessmann, Alexandre Reymond. Nat Genet 2009
224
50

Immunological Basis for Recurrent Fetal Loss and Pregnancy Complications.
Hitesh Deshmukh, Sing Sing Way. Annu Rev Pathol 2019
33
50

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
20
50

Array comparative genomic hybridization and flow cytometry analysis of spontaneous abortions and mors in utero samples.
Björn Menten, Katrien Swerts, Barbara Delle Chiaie, Sandra Janssens, Karen Buysse, Jan Philippé, Frank Speleman. BMC Med Genet 2009
51
50

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
141
50

1(st) trimester miscarriage: four decades of study.
Kathy Hardy, Philip John Hardy. Transl Pediatr 2015
25
50

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
50

A Comparison Between Two Assays for Measuring Seminal Oxidative Stress and their Relationship with Sperm DNA Fragmentation and Semen Parameters.
Sheryl T Homa, Anna M Vassiliou, Jesse Stone, Aideen P Killeen, Andrew Dawkins, Jingyi Xie, Farley Gould, Jonathan W A Ramsay. Genes (Basel) 2019
33
50

Is the incidence of recurrent pregnancy loss increasing? A retrospective register-based study in Sweden.
Emma Rasmark Roepke, Leif Matthiesen, Rebecca Rylance, Ole Bjarne Christiansen. Acta Obstet Gynecol Scand 2017
20
50

Genome-wide association study identified new susceptibility loci for polycystic ovary syndrome.
Hyejin Lee, Jee-Young Oh, Yeon-Ah Sung, Hyewon Chung, Hyung-Lae Kim, Gwang Sub Kim, Yoon Shin Cho, Jin Taek Kim. Hum Reprod 2015
40
50

New insights into mechanisms behind miscarriage.
Elisabeth Clare Larsen, Ole Bjarne Christiansen, Astrid Marie Kolte, Nick Macklon. BMC Med 2013
199
50

Deletions in 16q24.2 are associated with autism spectrum disorder, intellectual disability and congenital renal malformation.
Gregory Ryan Handrigan, David Chitayat, Anath C Lionel, Maury Pinsk, Andrea K Vaags, Christian R Marshall, Sarah Dyack, Luis F Escobar, Bridget A Fernandez, Joseph C Stegman,[...]. J Med Genet 2013
21
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.