A citation-based method for searching scientific literature

Cechuan Deng, Sau Wai Cheung, Hongqian Liu. Expert Rev Mol Diagn 2021
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity



Non invasive prenatal testing (NIPT) for common aneuploidies and beyond.
Medhat Sabry Alberry, Ehab Aziz, Sawssan R Ahmed, Sherif Abdel-Fattah. Eur J Obstet Gynecol Reprod Biol 2021
7
66

Screening, prenatal diagnosis, and prenatal decision for sex chromosome aneuploidy.
Yong Xu, Liyuan Chen, Yang Liu, Ying Hao, Zhiyong Xu, Liyanyan Deng, Jiansheng Xie. Expert Rev Mol Diagn 2019
13
66

Clinical experience with sex chromosome aneuploidies detected by noninvasive prenatal testing (NIPT): Accuracy and patient decision-making.
Aarti Ramdaney, Jennifer Hoskovec, Jacqueline Harkenrider, Eleazar Soto, Lauren Murphy. Prenat Diagn 2018
27
66

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
289
66

Outcome of publicly funded nationwide first-tier noninvasive prenatal screening.
Kris Van Den Bogaert, Lore Lannoo, Nathalie Brison, Vincent Gatinois, Machteld Baetens, Bettina Blaumeiser, François Boemer, Laura Bourlard, Vincent Bours, Anne De Leener,[...]. Genet Med 2021
17
66


Triple X syndrome: a review of the literature.
Maarten Otter, Constance T R M Schrander-Stumpel, Leopold M G Curfs. Eur J Hum Genet 2010
99
33

Abortion Stigma: A Systematic Review.
Franz Hanschmidt, Katja Linde, Anja Hilbert, Steffi G Riedel-Heller, Anette Kersting. Perspect Sex Reprod Health 2016
88
33

There can be no moral obligation to eradicate all disability.
Rebecca Bennett. Camb Q Healthc Ethics 2014
5
33

Family experiences and attitudes about receiving the diagnosis of sex chromosome aneuploidy in a child.
Kirsten A Riggan, Sharron Close, Megan A Allyse. Am J Med Genet C Semin Med Genet 2020
5
33

Providing Unrestricted Access to Prenatal Testing Does Not Translate to Enhanced Autonomy.
Vardit Ravitsky, Francois Rousseau, Anne-Marie Laberge. Am J Bioeth 2017
10
33

Decision outcomes in women offered noninvasive prenatal test (NIPT) for positive Down screening results.
Tsz-Kin Lo, Kelvin Yuen-Kwong Chan, Anita Sik-Yau Kan, Po-Lam So, Choi-Wah Kong, Shui-Lam Mak, Chung-Nin Lee. J Matern Fetal Neonatal Med 2019
13
33

Is bipolar disorder more common in highly intelligent people? A cohort study of a million men.
C R Gale, G D Batty, A M McIntosh, D J Porteous, I J Deary, F Rasmussen. Mol Psychiatry 2013
44
33

Termination of pregnancy following a prenatal diagnosis of Down syndrome: A qualitative study of the decision-making process of pregnant couples.
Stina Lou, Kathrine Carstensen, Olav Bjørn Petersen, Camilla Palmhøj Nielsen, Lone Hvidman, Maja Retpen Lanther, Ida Vogel. Acta Obstet Gynecol Scand 2018
20
33

The sudden death of the combined first trimester aneuploidy screening, a single centre experience in Belgium.
Jan Van Elslande, Nathalie Brison, Joris R Vermeesch, Koenraad Devriendt, Kris Van Den Bogaert, Eric Legius, Marc Van Ranst, Pieter Vermeersch, Jaak Billen. Clin Chem Lab Med 2019
2
50

Polygenic inheritance, GWAS, polygenic risk scores, and the search for functional variants.
Daniel J M Crouch, Walter F Bodmer. Proc Natl Acad Sci U S A 2020
31
33

In defence of Procreative Beneficence.
Julian Savulescu. J Med Ethics 2007
32
33

Implementing non-invasive prenatal testing (NIPT) in the Netherlands: An interview study exploring opinions about and experiences with societal pressure, reimbursement, and an expanding scope.
Iris M Bakkeren, Adriana Kater-Kuipers, Eline M Bunnik, Attie T J I Go, Aad Tibben, Inez D de Beaufort, Robert-Jan H Galjaard, Sam R Riedijk. J Genet Couns 2020
11
33

Noninvasive prenatal testing in routine clinical practice--an audit of NIPT and combined first-trimester screening in an unselected Australian population.
Andrew McLennan, Ricardo Palma-Dias, Fabricio da Silva Costa, Simon Meagher, Debbie L Nisbet, Fergus Scott. Aust N Z J Obstet Gynaecol 2016
28
33

Reproductive liberty, disease and disability.
John Harris. Reprod Biomed Online 2005
10
33



Genetic Prediction.
Eric Turkheimer. Hastings Cent Rep 2015
8
33

From GWAS to PheWAS: the search for causality in big data.
Jonathan Y Huang, Jeremy A Labrecque. Lancet Digit Health 2019
7
33

Prenatal exposure to mixture of heavy metals, pesticides and phenols and IQ in children at 7 years of age: The SMBCS study.
Jianqiu Guo, Chunhua Wu, Jiming Zhang, Xiaojuan Qi, Shenliang Lv, Shuai Jiang, Tong Zhou, Dasheng Lu, Chao Feng, Xiuli Chang,[...]. Environ Int 2020
23
33

Mainstreaming informed consent for genomic sequencing: A call for action.
Eline M Bunnik, Wybo J Dondorp, Annelien L Bredenoord, Guido de Wert, Martina C Cornel. Eur J Cancer 2021
5
33

Clinical and Economic Impact of Adopting Noninvasive Prenatal Testing as a Primary Screening Method for Fetal Aneuploidies in the General Pregnancy Population.
Emilia Kostenko, Frederic Chantraine, Katleen Vandeweyer, Maximilian Schmid, Alex Lefevre, Deanna Hertz, Laura Zelle, Jose Luis Bartha, Gian Carlo Di Renzo. Fetal Diagn Ther 2019
12
33

Premorbid intelligence and educational level in bipolar and unipolar disorders: a Danish draft board study.
Holger Jelling Sørensen, Ditte Sæbye, Annick Urfer-Parnas, Erik Lykke Mortensen, Josef Parnas. J Affect Disord 2012
21
33

The right to an open future concerning genetic information.
Annelien L Bredenoord, Martine C de Vries, Hans van Delden. Am J Bioeth 2014
16
33

Facilitating informed choice about non-invasive prenatal testing (NIPT): a systematic review and qualitative meta-synthesis of women's experiences.
Alexandra Cernat, Chante De Freitas, Umair Majid, Forum Trivedi, Caroline Higgins, Meredith Vanstone. BMC Pregnancy Childbirth 2019
32
33


Medical paternalism and the fetus.
J Wyatt. J Med Ethics 2001
15
33

Noninvasive prenatal testing for fetal aneuploidy and single gene disorders.
Hannah Skrzypek, Lisa Hui. Best Pract Res Clin Obstet Gynaecol 2017
29
33

Expanding the phenotype of Triple X syndrome: A comparison of prenatal versus postnatal diagnosis.
Kristen Wigby, Cheryl D'Epagnier, Susan Howell, Amy Reicks, Rebecca Wilson, Lisa Cordeiro, Nicole Tartaglia. Am J Med Genet A 2016
34
33

Has noninvasive prenatal testing impacted termination of pregnancy and live birth rates of infants with Down syndrome?
Melissa Hill, Angela Barrett, Mahesh Choolani, Celine Lewis, Jane Fisher, Lyn S Chitty. Prenat Diagn 2017
32
33

Penetrance and Pleiotropy of Polygenic Risk Scores for Schizophrenia in 106,160 Patients Across Four Health Care Systems.
Amanda B Zheutlin, Jessica Dennis, Richard Karlsson Linnér, Arden Moscati, Nicole Restrepo, Peter Straub, Douglas Ruderfer, Victor M Castro, Chia-Yen Chen, Tian Ge,[...]. Am J Psychiatry 2019
70
33

Retrospective details of false-positive and false-negative results in non-invasive prenatal testing for fetal trisomies 21, 18 and 13.
Nobuhiro Suzumori, Akihiko Sekizawa, Eri Takeda, Osamu Samura, Aiko Sasaki, Rina Akaishi, Seiji Wada, Haruka Hamanoue, Fumiki Hirahara, Hideaki Sawai,[...]. Eur J Obstet Gynecol Reprod Biol 2021
7
33

'Doctor, what would you do in my position?' Health professionals and the decision-making process in pregnancy monitoring.
Solène Gouilhers Hertig, Samuele Cavalli, Claudine Burton-Jeangros, Bernice S Elger. J Med Ethics 2014
12
33


PREIMPLANTATION GENETIC TESTING: Preimplantation genetic testing for polygenic disease risk.
Nathan R Treff, Diego Marin, Louis Lello, Stephen Hsu, Laurent C A M Tellier. Reproduction 2020
6
33

High risk-What's next? A survey study on decisional conflict, regret, and satisfaction among high-risk pregnant women making choices about further prenatal testing for fetal aneuploidy.
Tanja Schlaikjaer Hartwig, Caroline Borregaard Miltoft, Charlotta Ingvoldstad Malmgren, Ann Tabor, Finn Stener Jørgensen. Prenat Diagn 2019
14
33


Social and medical need for whole genome high resolution NIPT.
Malgorzata I Srebniak, Maarten F C M Knapen, Lutgarde C P Govaerts, Marike Polak, Marieke Joosten, Karin E M Diderich, Laura J C M van Zutven, Krista A K E Prinsen, Sam Riedijk, Attie T J I Go,[...]. Mol Genet Genomic Med 2020
5
33


Evaluating the Concept of Choice in Healthcare.
Yusrita Zolkefli. Malays J Med Sci 2017
13
33

Childhood intelligence in relation to major causes of death in 68 year follow-up: prospective population study.
Catherine M Calvin, G David Batty, Geoff Der, Caroline E Brett, Adele Taylor, Alison Pattie, Iva Čukić, Ian J Deary. BMJ 2017
63
33

How will new genetic technologies, such as gene editing, change reproductive decision-making? Views of high-risk couples.
Ivy van Dijke, Phillis Lakeman, Inge B Mathijssen, Mariëtte Goddijn, Martina C Cornel, Lidewij Henneman. Eur J Hum Genet 2021
2
50

What are the goals of prenatal genetic testing?
Stephanie Dukhovny, Mary E Norton. Semin Perinatol 2018
8
33



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.