A citation-based method for searching scientific literature

S Stern, N Hacohen, V Meiner, S Yagel, S Zenvirt, S Shkedi-Rafid, M Macarov, D V Valsky, S Porat, N Yanai, A Frumkin, H Daum. Ultrasound Obstet Gynecol 2021
Times Cited: 8







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



Times Cited
  Times     Co-cited
Similarity


Chromosomal microarray vs. NIPS: analysis of 5541 low-risk pregnancies.
Lena Sagi-Dain, Lital Cohen Vig, Sarit Kahana, Shiri Yacobson, Tamar Tenne, Ifat Agmon-Fishman, Cochava Klein, Reut Matar, Lina Basel-Salmon, Idit Maya. Genet Med 2019
31
37

Risk of miscarriage following amniocentesis or chorionic villus sampling: systematic review of literature and updated meta-analysis.
L J Salomon, A Sotiriadis, C B Wulff, A Odibo, R Akolekar. Ultrasound Obstet Gynecol 2019
81
37

Frequency of submicroscopic chromosomal aberrations in pregnancies without increased risk for structural chromosomal aberrations: systematic review and meta-analysis.
M I Srebniak, M Joosten, M F C M Knapen, L R Arends, M Polak, S van Veen, A T J I Go, D Van Opstal. Ultrasound Obstet Gynecol 2018
40
37

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
643
37

Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challenges.
Olivier Vanakker, Catheline Vilain, Katrien Janssens, Nathalie Van der Aa, Guillaume Smits, Claude Bandelier, Bettina Blaumeiser, Saskia Bulk, Jean-Hubert Caberg, Anne De Leener,[...]. Eur J Med Genet 2014
61
25

ACOG and SMFM guidelines for prenatal diagnosis: Is karyotyping really sufficient?
Sara B Hay, Trilochan Sahoo, Mary K Travis, Karine Hovanes, Natasa Dzidic, Charles Doherty, Michelle N Strecker. Prenat Diagn 2018
31
25

Estimates of penetrance for recurrent pathogenic copy-number variations.
Jill A Rosenfeld, Bradley P Coe, Evan E Eichler, Howard Cuckle, Lisa G Shaffer. Genet Med 2013
184
25

Pandora's pregnancy: NIPT, CMA, and genome sequencing-A new era for prenatal genetic testing.
Yael Hashiloni-Dolev, Tamar Nov-Klaiman, Aviad Raz. Prenat Diagn 2019
10
25

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
25



European guidelines for constitutional cytogenomic analysis.
Marisa Silva, Nicole de Leeuw, Kathy Mann, Heleen Schuring-Blom, Sian Morgan, Daniela Giardino, Katrina Rack, Ros Hastings. Eur J Hum Genet 2019
31
25

Prenatal diagnosis by chromosomal microarray analysis.
Brynn Levy, Ronald Wapner. Fertil Steril 2018
89
25


Benefits and burdens of using a SNP array in pregnancies at increased risk for the common aneuploidies.
Diane Van Opstal, Femke de Vries, Lutgarde Govaerts, Marjan Boter, Debora Lont, Stefanie van Veen, Marieke Joosten, Karin Diderich, Robert-Jan Galjaard, Malgorzata I Srebniak. Hum Mutat 2015
41
25

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
513
25

Experience with microarray-based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnancies.
Lisa G Shaffer, Mindy P Dabell, Allan J Fisher, Justine Coppinger, Anne M Bandholz, Jay W Ellison, J Britt Ravnan, Beth S Torchia, Blake C Ballif, Jill A Rosenfeld. Prenat Diagn 2012
136
25

Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysis.
S C Hillman, D J McMullan, G Hall, F S Togneri, N James, E J Maher, C H Meller, D Williams, R J Wapner, E R Maher,[...]. Ultrasound Obstet Gynecol 2013
154
25


High-resolution chromosomal microarrays in prenatal diagnosis significantly increase diagnostic power.
Beatrice Oneda, Rosa Baldinger, Regina Reissmann, Irina Reshetnikova, Pavel Krejci, Rahim Masood, Nicole Ochsenbein-Kölble, Deborah Bartholdi, Katharina Steindl, Denise Morotti,[...]. Prenat Diagn 2014
29
25

Information Women Choose to Receive About Prenatal Chromosomal Microarray Analysis.
Hagit Hochner, Hagit Daum, Liza Douiev, Naama Zvi, Ayala Frumkin, Michal Macarov, Adva Kimchi-Shaal, Nuphar Hacohen, Avital Eilat, Duha Faham,[...]. Obstet Gynecol 2020
6
33

Offering pregnant women different levels of genetic information from prenatal chromosome microarray: a prospective study.
Jane L Halliday, Cecile Muller, Taryn Charles, Fiona Norris, Joanne Kennedy, Sharon Lewis, Bettina Meiser, Susan Donath, Zornitza Stark, George McGillivray,[...]. Eur J Hum Genet 2018
11
25

Role of late amniocentesis in the era of modern genomic technologies.
H Daum, A Ben David, M Nadjari, S Zenvirt, S Helman, N Yanai, V Meiner, S Yagel, A Frumkin, S Shkedi Rafid. Ultrasound Obstet Gynecol 2019
7
28

Prenatal diagnosis in advanced maternal age. Amniocentesis or CVS, a patient's choice or lack of information?
H Brandenburg, L van der Zwan, M G Jahoda, T Stijnen, J W Wladimiroff. Prenat Diagn 1991
6
16


Pre Gestational Thalassemia Screening in Mainland China: The First Two Years of a Preventive Program.
Fan Jiang, Gui-Lan Chen, Jian Li, Xing-Mei Xie, Jian-Ying Zhou, Can Liao, Dong-Zhi Li. Hemoglobin 2017
12
12

Impact of cell-free fetal DNA on invasive prenatal diagnostic tests in a real-world public setting.
Ignacio Herraiz, Ana Villalba, Eliam Ajuria, Alba Barasoain, Ana Mendoza, Nazaret Pizarro, David Escribano, Alberto Galindo. J Perinat Med 2019
2
50

Clinical results after the implementation of cell-free fetal DNA detection in maternal plasma.
Cristina Martínez-Payo, Isabel Bada-Bosch, María Martínez-Moya, Tirso Pérez-Medina. J Obstet Gynaecol Res 2018
4
25

Patient's choice between a non-invasive prenatal test and invasive prenatal diagnosis based on test accuracy.
Yiu Man Chan, Tak Yeung Leung, Oi Ka Catherine Chan, Yvonne Kwun Yue Cheng, Daljit Singh Sahota. Fetal Diagn Ther 2014
8
12

Abnormal nuchal translucency: residual risk with normal cell-free DNA screening.
Tracy B Grossman, Kimberly L Bodenlos, Stephen T Chasen. J Matern Fetal Neonatal Med 2020
3
33

Should cell-free DNA testing be used in pregnancy with increased fetal nuchal translucency?
J Miranda, F Paz Y Miño, V Borobio, C Badenas, L Rodriguez-Revenga, M Pauta, A Borrell. Ultrasound Obstet Gynecol 2020
5
20

Analysis of cell-free DNA in maternal blood in screening for aneuploidies: updated meta-analysis.
M M Gil, V Accurti, B Santacruz, M N Plana, K H Nicolaides. Ultrasound Obstet Gynecol 2017
234
12

Non-invasive cell-free fetal DNA testing for aneuploidy: multicenter study of 31 515 singleton pregnancies in southeastern China.
L Xu, H Huang, N Lin, Y Wang, D He, M Zhang, M Chen, L Chen, Y Lin. Ultrasound Obstet Gynecol 2020
12
12

Feasibility of couple-based expanded carrier screening offered by general practitioners.
Juliette Schuurmans, Erwin Birnie, Lieke M van den Heuvel, Mirjam Plantinga, Anneke Lucassen, Dorina M van der Kolk, Kristin M Abbott, Adelita V Ranchor, Agnes D Diemers, Irene M van Langen. Eur J Hum Genet 2019
16
12

The uptake of pan-ethnic expanded carrier screening is higher when offered during preconception or early prenatal genetic counseling.
Dana Larsen, Jingmei Ma, Melissa Strassberg, Rajesh Ramakrishnan, Ignatia B Van den Veyver. Prenat Diagn 2019
6
16


Fetal Genotyping in Maternal Blood by Digital PCR: Towards NIPD of Monogenic Disorders Independently of Parental Origin.
Sara Perlado, Ana Bustamante-Aragonés, Marta Donas, Isabel Lorda-Sánchez, Javier Plaza, Marta Rodríguez de Alba. PLoS One 2016
21
12

Recent developments in genetic/genomic medicine.
Rachel H Horton, Anneke M Lucassen. Clin Sci (Lond) 2019
22
12

Ethical aspects of genetic counselling.
M J Seller. J Med Ethics 1982
10
12


Genome sequencing in healthcare: understanding the UK general public's views and implications for clinical practice.
Lisa M Ballard, Rachel H Horton, Angela Fenwick, Anneke M Lucassen. Eur J Hum Genet 2020
2
50

Representing a "revolution": how the popular press has portrayed personalized medicine.
Alessandro R Marcon, Mark Bieber, Timothy Caulfield. Genet Med 2018
29
12




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
12

An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities.
Erin B Kaminsky, Vineith Kaul, Justin Paschall, Deanna M Church, Brian Bunke, Dawn Kunig, Daniel Moreno-De-Luca, Andres Moreno-De-Luca, Jennifer G Mulle, Stephen T Warren,[...]. Genet Med 2011
286
12

Choosing between Higher and Lower Resolution Microarrays: do Pregnant Women Have Sufficient Knowledge to Make Informed Choices Consistent with their Attitude?
S L van der Steen, E M Bunnik, M G Polak, K E M Diderich, J Verhagen-Visser, L C P Govaerts, M Joosten, M F C M Knapen, A T J I Go, D Van Opstal,[...]. J Genet Couns 2018
9
12

Non-invasive Prenatal Testing Using Fetal DNA.
Giulia Breveglieri, Elisabetta D'Aversa, Alessia Finotti, Monica Borgatti. Mol Diagn Ther 2019
22
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.