A citation-based method for searching scientific literature

Stephen C Collins. J Assist Reprod Genet 2017
Times Cited: 8







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



Times Cited
  Times     Co-cited
Similarity


Personalized reproductive medicine on the brink: progress, opportunities and challenges ahead.
Piraye Yurttas Beim, Michael Elashoff, Tina T Hu-Seliger. Reprod Biomed Online 2013
9
62

Bearings in Hip Arthroplasty: Joint Registries vs Precision Medicine: Review Article.
Mark J Pearson, Liam M Grover, Janet M Lord, Simon W Jones, Edward T Davis. HSS J 2017
5
40



Precision Medicine: The new era in medicine.
Marinka Twilt. EBioMedicine 2016
11
25

Seminal biomarkers for the evaluation of male infertility.
Jared M Bieniek, Andrei P Drabovich, Kirk C Lo. Asian J Androl 2016
47
25

The use of genomics, proteomics, and metabolomics in identifying biomarkers of male infertility.
Jason R Kovac, Alexander W Pastuszak, Dolores J Lamb. Fertil Steril 2013
123
25


A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
25

Precision Medicine and Men's Health.
Douglas A Mata, Farhan M Katchi, Ranjith Ramasamy. Am J Mens Health 2017
8
25

At the dawn of personalized reproductive medicine: opportunities and challenges with incorporating multigene panel testing into fertility care.
Piraye Yurttas Beim, David-Emlyn Parfitt, Lei Tan, Elaine A Sugarman, Tina Hu-Seliger, Caterina Clementi, Brynn Levy. J Assist Reprod Genet 2017
4
50

Biomarkers in reproductive medicine: the quest for new answers.
Carlos Simon, Denny Sakkas, David K Gardner, Hilary O D Critchley. Hum Reprod Update 2015
5
20

Personalized assisted reproductive technology.
Carlos Simón. Fertil Steril 2013
6
16

Mutational screening of the coding region of growth differentiation factor 9 gene in Indian women with ovarian failure.
Hridesh Dixit, Lakshmi K Rao, Venkata Padmalatha, Murthy Kanakavalli, Mamatha Deenadayal, Nalini Gupta, Baidyanath Chakravarty, Lalji Singh. Menopause 2005
106
12


Risk factor changes for sudden infant death syndrome after initiation of Back-to-Sleep campaign.
Felicia L Trachtenberg, Elisabeth A Haas, Hannah C Kinney, Christina Stanley, Henry F Krous. Pediatrics 2012
92
12

PI3K/PTEN/Akt and TSC/mTOR signaling pathways, ovarian dysfunction, and infertility: an update.
Annu Makker, Madhu Mati Goel, Abbas Ali Mahdi. J Mol Endocrinol 2014
93
12

American Society of Clinical Oncology provisional clinical opinion: epidermal growth factor receptor (EGFR) Mutation testing for patients with advanced non-small-cell lung cancer considering first-line EGFR tyrosine kinase inhibitor therapy.
Vicki Leigh Keedy, Sarah Temin, Mark R Somerfield, Mary Beth Beasley, David H Johnson, Lisa M McShane, Daniel T Milton, John R Strawn, Heather A Wakelee, Giuseppe Giaccone. J Clin Oncol 2011
394
12

In humans, zona pellucida glycoprotein-1 binds to spermatozoa and induces acrosomal exocytosis.
Anasua Ganguly, Antonin Bukovsky, Raj K Sharma, Pankaj Bansal, Beena Bhandari, Satish K Gupta. Hum Reprod 2010
38
12


Smoking and female infertility: a systematic review and meta-analysis.
C Augood, K Duckitt, A A Templeton. Hum Reprod 1998
238
12



Evaluating the Clinical Validity of Gene-Disease Associations: An Evidence-Based Framework Developed by the Clinical Genome Resource.
Natasha T Strande, Erin Rooney Riggs, Adam H Buchanan, Ozge Ceyhan-Birsoy, Marina DiStefano, Selina S Dwight, Jenny Goldstein, Rajarshi Ghosh, Bryce A Seifert, Tam P Sneddon,[...]. Am J Hum Genet 2017
188
12

A national survey on public perceptions of miscarriage.
Jonah Bardos, Daniel Hercz, Jenna Friedenthal, Stacey A Missmer, Zev Williams. Obstet Gynecol 2015
58
12


Role of chemokines in the endometrium and in embryo implantation.
Natalie J Hannan, Lois A Salamonsen. Curr Opin Obstet Gynecol 2007
74
12

High-Throughput Genomics and Clinical Outcome in Hard-to-Treat Advanced Cancers: Results of the MOSCATO 01 Trial.
Christophe Massard, Stefan Michiels, Charles Ferté, Marie-Cécile Le Deley, Ludovic Lacroix, Antoine Hollebecque, Loic Verlingue, Ecaterina Ileana, Silvia Rosellini, Samy Ammari,[...]. Cancer Discov 2017
259
12

Mutant ZP1 in familial infertility.
Hua-Lin Huang, Chao Lv, Ying-Chun Zhao, Wen Li, Xue-Mei He, Ping Li, Ai-Guo Sha, Xiao Tian, Christopher J Papasian, Hong-Wen Deng,[...]. N Engl J Med 2014
56
12


Single nucleotide polymorphisms in premature ovarian failure-associated genes in a Chinese Hui population.
Lili Ma, Yan Chen, Si Mei, Chunlian Liu, Xiaohong Ma, Yongli Li, Yinzhi Jiang, Lingxia Ha, Xian Xu. Mol Med Rep 2015
13
12

Inflammation and Human Ovarian Follicular Dynamics.
Christina E Boots, Emily S Jungheim. Semin Reprod Med 2015
62
12

The endocrine and paracrine control of menstruation.
Patrick Henriet, Héloïse P Gaide Chevronnay, Etienne Marbaix. Mol Cell Endocrinol 2012
46
12


A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders.
Zornitza Stark, Tiong Y Tan, Belinda Chong, Gemma R Brett, Patrick Yap, Maie Walsh, Alison Yeung, Heidi Peters, Dylan Mordaunt, Shannon Cowie,[...]. Genet Med 2016
190
12

Exome sequencing reveals a nonsense mutation in TEX15 causing spermatogenic failure in a Turkish family.
Ozlem Okutman, Jean Muller, Yoni Baert, Munevver Serdarogullari, Meral Gultomruk, Amélie Piton, Charlotte Rombaut, Moncef Benkhalifa, Marius Teletin, Valerie Skory,[...]. Hum Mol Genet 2015
61
12

The clinical application of genome-wide sequencing for monogenic diseases in Canada: Position Statement of the Canadian College of Medical Geneticists.
Kym Boycott, Taila Hartley, Shelin Adam, Francois Bernier, Karen Chong, Bridget A Fernandez, Jan M Friedman, Michael T Geraghty, Stacey Hume, Bartha M Knoppers,[...]. J Med Genet 2015
115
12

Molecular findings among patients referred for clinical whole-exome sequencing.
Yaping Yang, Donna M Muzny, Fan Xia, Zhiyv Niu, Richard Person, Yan Ding, Patricia Ward, Alicia Braxton, Min Wang, Christian Buhay,[...]. JAMA 2014
792
12

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
29
12

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf,[...]. Genet Med 2017
799
12

Clinical exome sequencing: results from 2819 samples reflecting 1000 families.
Daniel Trujillano, Aida M Bertoli-Avella, Krishna Kumar Kandaswamy, Maximilian Er Weiss, Julia Köster, Anett Marais, Omid Paknia, Rolf Schröder, Jose Maria Garcia-Aznar, Martin Werber,[...]. Eur J Hum Genet 2017
172
12

Exploring the utility of whole-exome sequencing as a diagnostic tool in a child with atypical episodic muscle weakness.
Neil A Hanchard, David R Murdock, Pilar L Magoulas, Matthew Bainbridge, Donna Muzny, YuanQing Wu, Min Wang, James R Lupski, Richard A Gibbs, Chester W Brown. Clin Genet 2013
21
12

What is the clinical utility of genetic testing?
Scott D Grosse, Muin J Khoury. Genet Med 2006
171
12

Whole-genome sequencing for optimized patient management.
Matthew N Bainbridge, Wojciech Wiszniewski, David R Murdock, Jennifer Friedman, Claudia Gonzaga-Jauregui, Irene Newsham, Jeffrey G Reid, John K Fink, Margaret B Morgan, Marie-Claude Gingras,[...]. Sci Transl Med 2011
176
12

Pre- and post-test genetic counseling for chromosomal and Mendelian disorders.
Jill Fonda Allen, Katie Stoll, Barbara A Bernhardt. Semin Perinatol 2016
12
12


Whole-exome sequencing identifies novel homozygous mutation in NPAS2 in family with nonobstructive azoospermia.
Ranjith Ramasamy, M Emre Bakırcıoğlu, Cenk Cengiz, Ender Karaca, Jason Scovell, Shalini N Jhangiani, Zeynep C Akdemir, Matthew Bainbridge, Yao Yu, Chad Huff,[...]. Fertil Steril 2015
39
12

Whole exome sequencing in recurrent early pregnancy loss.
Ying Qiao, Jiadi Wen, Flamingo Tang, Sally Martell, Naomi Shomer, Peter C K Leung, Mary D Stephenson, Evica Rajcan-Separovic. Mol Hum Reprod 2016
27
12

GeneMatcher: a matching tool for connecting investigators with an interest in the same gene.
Nara Sobreira, François Schiettecatte, David Valle, Ada Hamosh. Hum Mutat 2015
589
12

Inherited mutation of the luteinizing hormone/choriogonadotropin receptor (LHCGR) in empty follicle syndrome.
Kemal O Yariz, Tom Walsh, Asli Uzak, Michail Spiliopoulos, Duygu Duman, Gogsen Onalan, Mary-Claire King, Mustafa Tekin. Fertil Steril 2011
44
12


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.