A citation-based method for searching scientific literature

Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. Eur J Hum Genet 2013
Times Cited: 50







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



Times Cited
  Times     Co-cited
Similarity


Fetal surgery: principles, indications, and evidence.
Katharine D Wenstrom, Stephen R Carr. Obstet Gynecol 2014
13
7

Just choice: a Danielsian analysis of the aims and scope of prenatal screening for fetal abnormalities.
Greg Stapleton, Wybo Dondorp, Peter Schröder-Bäck, Guido de Wert. Med Health Care Philos 2019
5
20

Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA.
Jinglan Zhang, Jianli Li, Jennifer B Saucier, Yanming Feng, Yanjun Jiang, Jefferson Sinson, Anne K McCombs, Eric S Schmitt, Sandra Peacock, Stella Chen,[...]. Nat Med 2019
66
2

Next-generation sequencing and the impact on prenatal diagnosis.
Rhiannon Mellis, Natalie Chandler, Lyn S Chitty. Expert Rev Mol Diagn 2018
14
7

In Utero Gene Therapy Consensus Statement from the IFeTIS.
Graça Almeida-Porada, Simon N Waddington, Jerry K Y Chan, William H Peranteau, Tippi MacKenzie, Christopher D Porada. Mol Ther 2019
12
8

Dotting the I's and crossing the T's: autonomy and/or beneficence? The 'fetus as a patient' in maternal-fetal surgery.
H Catarina M L Rodrigues, Paul P van den Berg, Marcus Düwell. J Med Ethics 2013
4
25

Overview of the impact of noninvasive prenatal testing on diagnostic procedures.
Steven L Warsof, Sebastian Larion, Alfred Z Abuhamad. Prenat Diagn 2015
75
2

Unfair discrimination in prenatal aneuploidy screening using cell-free DNA?
Vasilija Rolfes, Dagmar Schmitz. Eur J Obstet Gynecol Reprod Biol 2016
6
16

Update on the use of exome sequencing in the diagnosis of fetal abnormalities.
Lauren Ferretti, Rhiannon Mellis, Lyn S Chitty. Eur J Med Genet 2019
16
6


Noninvasive Prenatal Whole Genome Sequencing: Pregnant Women's Views and Preferences.
Haley K Sullivan, Michelle Bayefsky, Paul G Wakim, Kathi Huddleston, Barbara B Biesecker, Sara Chandros Hull, Benjamin E Berkman. Obstet Gynecol 2019
10
10

Prenatal Correction of X-Linked Hypohidrotic Ectodermal Dysplasia.
Holm Schneider, Florian Faschingbauer, Sonia Schuepbach-Mallepell, Iris Körber, Sigrun Wohlfart, Angela Dick, Mandy Wahlbuhl, Christine Kowalczyk-Quintas, Michele Vigolo, Neil Kirby,[...]. N Engl J Med 2018
47
2


Fetal gene therapy for neurodegenerative disease of infants.
Giulia Massaro, Citra N Z Mattar, Andrew M S Wong, Ernestas Sirka, Suzanne M K Buckley, Bronwen R Herbert, Stefan Karlsson, Dany P Perocheau, Derek Burke, Simon Heales,[...]. Nat Med 2018
62
2

A critique of the 'fetus as patient'.
Anne Drapkin Lyerly, Margaret Olivia Little, Ruth R Faden. Am J Bioeth 2008
19
5

In case you missed it: The Prenatal Diagnosis editors bring you the most significant advances of 2017.
Brynn Levy, Diana W Bianchi, Tim Van Mieghem, Jan Deprest, Alessandro Ghidini, Lyn S Chitty. Prenat Diagn 2018
2
50

Ethical challenges in fetal surgery.
Anna Smajdor. J Med Ethics 2011
19
5


Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study.
Slavé Petrovski, Vimla Aggarwal, Jessica L Giordano, Melissa Stosic, Karen Wou, Louise Bier, Erica Spiegel, Kelly Brennan, Nicholas Stong, Vaidehi Jobanputra,[...]. Lancet 2019
112
2

Considerations for whole exome sequencing unique to prenatal care.
Ahmad Abou Tayoun, Heather Mason-Suares. Hum Genet 2020
6
16

A Brave New World of Bespoke Babies?
Tom Shakespeare. Am J Bioeth 2017
3
33

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
2

What are the goals of prenatal genetic testing?
Stephanie Dukhovny, Mary E Norton. Semin Perinatol 2018
4
25

Polyhydramnios, Transient Antenatal Bartter's Syndrome, and MAGED2 Mutations.
Kamel Laghmani, Bodo B Beck, Sung-Sen Yang, Elie Seaayfan, Andrea Wenzel, Björn Reusch, Helga Vitzthum, Dario Priem, Sylvie Demaretz, Klasien Bergmann,[...]. N Engl J Med 2016
68
2





Open fetal surgery for neural tube defects.
Julie S Moldenhauer, Alan W Flake. Best Pract Res Clin Obstet Gynaecol 2019
9
11

Concerns About Justification for Fetal Genome Sequencing.
Jeffrey R Botkin, Leslie P Francis, Nancy C Rose. Am J Bioeth 2017
8
12

Ethical and counseling challenges in prenatal exome sequencing.
Sarah Harris, Kelly Gilmore, Emily Hardisty, Anne Drapkin Lyerly, Neeta L Vora. Prenat Diagn 2018
12
8

Ethical considerations in prenatal testing: Genomic testing and medical uncertainty.
Anastasia Richardson, Kelly E Ormond. Semin Fetal Neonatal Med 2018
13
7


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.