Jing Yang, Min Chen, Xiaoqing Ye, Fei Chen, Yufan Li, Nan Li, Wenyan Wu, Jimei Sun. Eur J Obstet Gynecol Reprod Biol 2021
Times Cited: 3
Times Cited: 3
Times Cited
Times Co-cited
Similarity
Presence of fetal DNA in maternal plasma and serum.
Y M Lo, N Corbetta, P F Chamberlain, V Rai, I L Sargent, C W Redman, J S Wainscoat. Lancet 1997
Y M Lo, N Corbetta, P F Chamberlain, V Rai, I L Sargent, C W Redman, J S Wainscoat. Lancet 1997
66
Position statement from the Chromosome Abnormality Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis.
Peter Benn, Antoni Borrell, Rossa W K Chiu, Howard Cuckle, Lorraine Dugoff, Brigitte Faas, Susan Gross, Tianhua Huang, Joann Johnson, Ron Maymon,[...]. Prenat Diagn 2015
Peter Benn, Antoni Borrell, Rossa W K Chiu, Howard Cuckle, Lorraine Dugoff, Brigitte Faas, Susan Gross, Tianhua Huang, Joann Johnson, Ron Maymon,[...]. Prenat Diagn 2015
66
PREIMPLANTATION GENETIC TESTING: Non-invasive prenatal testing for aneuploidy, copy-number variants and single-gene disorders.
J Shaw, E Scotchman, N Chandler, L S Chitty. Reproduction 2020
J Shaw, E Scotchman, N Chandler, L S Chitty. Reproduction 2020
66
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
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
33
A first look at women's perspectives on noninvasive prenatal testing to detect sex chromosome aneuploidies and microdeletion syndromes.
Patricia K Agatisa, Mary Beth Mercer, Angela C Leek, Marissa B Smith, Elliot Philipson, Ruth M Farrell. Prenat Diagn 2015
Patricia K Agatisa, Mary Beth Mercer, Angela C Leek, Marissa B Smith, Elliot Philipson, Ruth M Farrell. Prenat Diagn 2015
33
Controversies in prenatal diagnosis 3: should everyone undergoing invasive testing have a microarray?
John A Crolla, Ronald Wapner, Jan M M Van Lith. Prenat Diagn 2014
John A Crolla, Ronald Wapner, Jan M M Van Lith. Prenat Diagn 2014
33
Noninvasive prenatal detection of sex chromosomal aneuploidies by sequencing circulating cell-free DNA from maternal plasma.
Amin R Mazloom, Željko Džakula, Paul Oeth, Huiquan Wang, Taylor Jensen, John Tynan, Ron McCullough, Juan-Sebastian Saldivar, Mathias Ehrich, Dirk van den Boom,[...]. Prenat Diagn 2013
Amin R Mazloom, Željko Džakula, Paul Oeth, Huiquan Wang, Taylor Jensen, John Tynan, Ron McCullough, Juan-Sebastian Saldivar, Mathias Ehrich, Dirk van den Boom,[...]. Prenat Diagn 2013
33
Detection of trisomy 21 by quantitative mass spectrometric analysis of single-nucleotide polymorphisms.
Nancy B Y Tsui, Rossa W K Chiu, Chunming Ding, Ahmad El-Sheikhah, Tse N Leung, Tze K Lau, Kypros H Nicolaides, Y M Dennis Lo. Clin Chem 2005
Nancy B Y Tsui, Rossa W K Chiu, Chunming Ding, Ahmad El-Sheikhah, Tse N Leung, Tze K Lau, Kypros H Nicolaides, Y M Dennis Lo. Clin Chem 2005
33
Noninvasive prenatal screening for fetal aneuploidy, 2016 update: a position statement of the American College of Medical Genetics and Genomics.
Anthony R Gregg, Brian G Skotko, Judith L Benkendorf, Kristin G Monaghan, Komal Bajaj, Robert G Best, Susan Klugman, Michael S Watson. Genet Med 2016
Anthony R Gregg, Brian G Skotko, Judith L Benkendorf, Kristin G Monaghan, Komal Bajaj, Robert G Best, Susan Klugman, Michael S Watson. Genet Med 2016
33
Detection rates of clinically significant genomic alterations by microarray analysis for specific anomalies detected by ultrasound.
Lisa G Shaffer, Jill A Rosenfeld, Mindy P Dabell, Justine Coppinger, Anne M Bandholz, Jay W Ellison, J Britt Ravnan, Beth S Torchia, Blake C Ballif, Allan J Fisher. Prenat Diagn 2012
Lisa G Shaffer, Jill A Rosenfeld, Mindy P Dabell, Justine Coppinger, Anne M Bandholz, Jay W Ellison, J Britt Ravnan, Beth S Torchia, Blake C Ballif, Allan J Fisher. Prenat Diagn 2012
33
The clinical utility of microarray technologies applied to prenatal cytogenetics in the presence of a normal conventional karyotype: a review of the literature.
Jonathan L A Callaway, Lisa G Shaffer, Lyn S Chitty, Jill A Rosenfeld, John A Crolla. Prenat Diagn 2013
Jonathan L A Callaway, Lisa G Shaffer, Lyn S Chitty, Jill A Rosenfeld, John A Crolla. Prenat Diagn 2013
33
Plasma placental RNA allelic ratio permits noninvasive prenatal chromosomal aneuploidy detection.
Y M Dennis Lo, Nancy B Y Tsui, Rossa W K Chiu, Tze K Lau, Tse N Leung, Macy M S Heung, Ageliki Gerovassili, Yongjie Jin, Kypros H Nicolaides, Charles R Cantor,[...]. Nat Med 2007
Y M Dennis Lo, Nancy B Y Tsui, Rossa W K Chiu, Tze K Lau, Tse N Leung, Macy M S Heung, Ageliki Gerovassili, Yongjie Jin, Kypros H Nicolaides, Charles R Cantor,[...]. Nat Med 2007
33
Clinical utility of noninvasive prenatal screening for expanded chromosome disease syndromes.
Desheng Liang, David S Cram, Hu Tan, Siyuan Linpeng, Yingdi Liu, Huaiyu Sun, Yu Zhang, Feng Tian, Hongmin Zhu, Mengnan Xu,[...]. Genet Med 2019
Desheng Liang, David S Cram, Hu Tan, Siyuan Linpeng, Yingdi Liu, Huaiyu Sun, Yu Zhang, Feng Tian, Hongmin Zhu, Mengnan Xu,[...]. Genet Med 2019
33
Cell-free DNA vs sequential screening for the detection of fetal chromosomal abnormalities.
Mary E Norton, Rebecca J Baer, Ronald J Wapner, Miriam Kuppermann, Laura L Jelliffe-Pawlowski, Robert J Currier. Am J Obstet Gynecol 2016
Mary E Norton, Rebecca J Baer, Ronald J Wapner, Miriam Kuppermann, Laura L Jelliffe-Pawlowski, Robert J Currier. Am J Obstet Gynecol 2016
33
Promoting safe and effective genetic testing in the United States. Final report of the Task Force on Genetic Testing.
N A Holtzman, M S Watson. J Child Fam Nurs 1999
N A Holtzman, M S Watson. J Child Fam Nurs 1999
33
Understanding attitudes and behaviors towards cell-free DNA-based noninvasive prenatal testing (NIPT): A survey of European health-care providers.
Alexandra Benachi, Jessica Caffrey, Pavel Calda, Elena Carreras, Jacques C Jani, Mark D Kilby, Hanns-Georg Klein, Giuseppe Rizzo, Yuval Yaron. Eur J Med Genet 2020
Alexandra Benachi, Jessica Caffrey, Pavel Calda, Elena Carreras, Jacques C Jani, Mark D Kilby, Hanns-Georg Klein, Giuseppe Rizzo, Yuval Yaron. Eur J Med Genet 2020
33
Prenatal screening in the era of non-invasive prenatal testing: a Nationwide cross-sectional survey of obstetrician knowledge, attitudes and clinical practice.
Liying Yang, Wei Ching Tan. BMC Pregnancy Childbirth 2020
Liying Yang, Wei Ching Tan. BMC Pregnancy Childbirth 2020
100
Survey of US obstetrician opinions regarding NIPT use in general practice: implementation and barriers.
Justin Brewer, Lisa Demers, Thomas Musci. J Matern Fetal Neonatal Med 2017
Justin Brewer, Lisa Demers, Thomas Musci. J Matern Fetal Neonatal Med 2017
33
Screening for Fetal Chromosomal Abnormalities: ACOG Practice Bulletin, Number 226.
. Obstet Gynecol 2020
. Obstet Gynecol 2020
33
Cell-free DNA analysis for noninvasive examination of trisomy.
Mary E Norton, Bo Jacobsson, Geeta K Swamy, Louise C Laurent, Angela C Ranzini, Herb Brar, Mark W Tomlinson, Leonardo Pereira, Jean L Spitz, Desiree Hollemon,[...]. N Engl J Med 2015
Mary E Norton, Bo Jacobsson, Geeta K Swamy, Louise C Laurent, Angela C Ranzini, Herb Brar, Mark W Tomlinson, Leonardo Pereira, Jean L Spitz, Desiree Hollemon,[...]. N Engl J Med 2015
33
Should we 'open the kimono' to release the results of rare autosomal aneuploidies following noninvasive prenatal whole genome sequencing?
Diana W Bianchi. Prenat Diagn 2017
Diana W Bianchi. Prenat Diagn 2017
33
Current controversies in prenatal diagnosis: Expanded NIPT that includes conditions other than trisomies 13, 18, and 21 should be offered.
Lieve Christiaens, Lyn S Chitty, Sylvie Langlois. Prenat Diagn 2021
Lieve Christiaens, Lyn S Chitty, Sylvie Langlois. Prenat Diagn 2021
33
Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma.
Rossa W K Chiu, K C Allen Chan, Yuan Gao, Virginia Y M Lau, Wenli Zheng, Tak Y Leung, Chris H F Foo, Bin Xie, Nancy B Y Tsui, Fiona M F Lun,[...]. Proc Natl Acad Sci U S A 2008
Rossa W K Chiu, K C Allen Chan, Yuan Gao, Virginia Y M Lau, Wenli Zheng, Tak Y Leung, Chris H F Foo, Bin Xie, Nancy B Y Tsui, Fiona M F Lun,[...]. Proc Natl Acad Sci U S A 2008
33
Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes.
Ronald J Wapner, Joshua E Babiarz, Brynn Levy, Melissa Stosic, Bernhard Zimmermann, Styrmir Sigurjonsson, Nicholas Wayham, Allison Ryan, Milena Banjevic, Phil Lacroute,[...]. Am J Obstet Gynecol 2015
Ronald J Wapner, Joshua E Babiarz, Brynn Levy, Melissa Stosic, Bernhard Zimmermann, Styrmir Sigurjonsson, Nicholas Wayham, Allison Ryan, Milena Banjevic, Phil Lacroute,[...]. Am J Obstet Gynecol 2015
33
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
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
33
Current controversies in prenatal diagnosis 3: the ethical and counseling implications of new genomic technologies: all pregnant women should be offered prenatal diagnostic genome-wide testing for prenatally identified fetal congenital anomalies.
R Douglas Wilson, David H Ledbetter, Eugene Pergament. Prenat Diagn 2015
R Douglas Wilson, David H Ledbetter, Eugene Pergament. Prenat Diagn 2015
33
The use of noninvasive prenatal testing in obstetric care: educational resources, practice patterns, and barriers reported by a national sample of clinicians.
Ruth M Farrell, Patricia K Agatisa, Mary Beth Mercer, Ariane G Mitchum, Marissa B Coleridge. Prenat Diagn 2016
Ruth M Farrell, Patricia K Agatisa, Mary Beth Mercer, Ariane G Mitchum, Marissa B Coleridge. Prenat Diagn 2016
33
Karyotype versus genomic hybridization for the prenatal diagnosis of chromosomal abnormalities: a metaanalysis.
Wilmar Saldarriaga, Herney Andrés García-Perdomo, Johanna Arango-Pineda, Javier Fonseca. Am J Obstet Gynecol 2015
Wilmar Saldarriaga, Herney Andrés García-Perdomo, Johanna Arango-Pineda, Javier Fonseca. Am J Obstet Gynecol 2015
33
Nearly a third of abnormalities found after first-trimester screening are different than expected: 10-year experience from a single center.
Christina M L Alamillo, David Krantz, Mark Evans, Morris Fiddler, Eugene Pergament. Prenat Diagn 2013
Christina M L Alamillo, David Krantz, Mark Evans, Morris Fiddler, Eugene Pergament. Prenat Diagn 2013
33
Couples experiences of receiving uncertain results following prenatal microarray or exome sequencing: A mixed-methods systematic review.
Eleanor Harding, Jennifer Hammond, Lyn S Chitty, Melissa Hill, Celine Lewis. Prenat Diagn 2020
Eleanor Harding, Jennifer Hammond, Lyn S Chitty, Melissa Hill, Celine Lewis. Prenat Diagn 2020
33
Noninvasive screening by cell-free DNA for 22q11.2 deletion: Benefits, limitations, and challenges.
Francesca Romana Grati, Susan J Gross. Prenat Diagn 2019
Francesca Romana Grati, Susan J Gross. Prenat Diagn 2019
33
Clinical outcome of subchromosomal events detected by whole-genome noninvasive prenatal testing.
J Helgeson, J Wardrop, T Boomer, E Almasri, W B Paxton, J S Saldivar, N Dharajiya, T J Monroe, D H Farkas, D S Grosu,[...]. Prenat Diagn 2015
J Helgeson, J Wardrop, T Boomer, E Almasri, W B Paxton, J S Saldivar, N Dharajiya, T J Monroe, D H Farkas, D S Grosu,[...]. Prenat Diagn 2015
33
Clinical experience with a single-nucleotide polymorphism-based non-invasive prenatal test for five clinically significant microdeletions.
K Martin, S Iyengar, A Kalyan, C Lan, A L Simon, M Stosic, K Kobara, H Ravi, T Truong, A Ryan,[...]. Clin Genet 2018
K Martin, S Iyengar, A Kalyan, C Lan, A L Simon, M Stosic, K Kobara, H Ravi, T Truong, A Ryan,[...]. Clin Genet 2018
33
Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood.
H Christina Fan, Yair J Blumenfeld, Usha Chitkara, Louanne Hudgins, Stephen R Quake. Proc Natl Acad Sci U S A 2008
H Christina Fan, Yair J Blumenfeld, Usha Chitkara, Louanne Hudgins, Stephen R Quake. Proc Natl Acad Sci U S A 2008
33
Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe.
Diana Wellesley, Helen Dolk, Patricia A Boyd, Ruth Greenlees, Martin Haeusler, Vera Nelen, Ester Garne, Babak Khoshnood, Berenice Doray, Anke Rissmann,[...]. Eur J Hum Genet 2012
Diana Wellesley, Helen Dolk, Patricia A Boyd, Ruth Greenlees, Martin Haeusler, Vera Nelen, Ester Garne, Babak Khoshnood, Berenice Doray, Anke Rissmann,[...]. Eur J Hum Genet 2012
33
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
M M Gil, V Accurti, B Santacruz, M N Plana, K H Nicolaides. Ultrasound Obstet Gynecol 2017
33
Global perspectives on clinical adoption of NIPT.
Mollie A Minear, Celine Lewis, Subarna Pradhan, Subhashini Chandrasekharan. Prenat Diagn 2015
Mollie A Minear, Celine Lewis, Subarna Pradhan, Subhashini Chandrasekharan. Prenat Diagn 2015
33
Noninvasive prenatal screening or advanced diagnostic testing: caveat emptor.
Mark I Evans, Ronald J Wapner, Richard L Berkowitz. Am J Obstet Gynecol 2016
Mark I Evans, Ronald J Wapner, Richard L Berkowitz. Am J Obstet Gynecol 2016
33
TRIDENT-2: National Implementation of Genome-wide Non-invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands.
Karuna R M van der Meij, Erik A Sistermans, Merryn V E Macville, Servi J C Stevens, Caroline J Bax, Mireille N Bekker, Caterina M Bilardo, Elles M J Boon, Marjan Boter, Karin E M Diderich,[...]. Am J Hum Genet 2019
Karuna R M van der Meij, Erik A Sistermans, Merryn V E Macville, Servi J C Stevens, Caroline J Bax, Mireille N Bekker, Caterina M Bilardo, Elles M J Boon, Marjan Boter, Karin E M Diderich,[...]. Am J Hum Genet 2019
33
Uptake, outcomes, and costs of implementing non-invasive prenatal testing for Down's syndrome into NHS maternity care: prospective cohort study in eight diverse maternity units.
Lyn S Chitty, David Wright, Melissa Hill, Talitha I Verhoef, Rebecca Daley, Celine Lewis, Sarah Mason, Fiona McKay, Lucy Jenkins, Abigail Howarth,[...]. BMJ 2016
Lyn S Chitty, David Wright, Melissa Hill, Talitha I Verhoef, Rebecca Daley, Celine Lewis, Sarah Mason, Fiona McKay, Lucy Jenkins, Abigail Howarth,[...]. BMJ 2016
33
Genomic microarray in fetuses with increased nuchal translucency and normal karyotype: a systematic review and meta-analysis.
M Grande, F A R Jansen, Y J Blumenfeld, A Fisher, A O Odibo, M C Haak, A Borrell. Ultrasound Obstet Gynecol 2015
M Grande, F A R Jansen, Y J Blumenfeld, A Fisher, A O Odibo, M C Haak, A Borrell. Ultrasound Obstet Gynecol 2015
33
Obstetrical provider knowledge and attitudes towards cell-free DNA screening: results of a cross-sectional national survey.
Wilson V Chan, Jo-Ann Johnson, R Douglas Wilson, Amy Metcalfe. BMC Pregnancy Childbirth 2018
Wilson V Chan, Jo-Ann Johnson, R Douglas Wilson, Amy Metcalfe. BMC Pregnancy Childbirth 2018
33
Rare autosomal trisomies, revealed by maternal plasma DNA sequencing, suggest increased risk of feto-placental disease.
Mark D Pertile, Meredith Halks-Miller, Nicola Flowers, Catalin Barbacioru, Sarah L Kinnings, Darcy Vavrek, William K Seltzer, Diana W Bianchi. Sci Transl Med 2017
Mark D Pertile, Meredith Halks-Miller, Nicola Flowers, Catalin Barbacioru, Sarah L Kinnings, Darcy Vavrek, William K Seltzer, Diana W Bianchi. Sci Transl Med 2017
33
Non-invasive prenatal testing for the prenatal screening of sex chromosome aneuploidies: A systematic review and meta-analysis of diagnostic test accuracy studies.
Bounhome Soukkhaphone, Carmen Lindsay, Sylvie Langlois, Julian Little, Francois Rousseau, Daniel Reinharz. Mol Genet Genomic Med 2021
Bounhome Soukkhaphone, Carmen Lindsay, Sylvie Langlois, Julian Little, Francois Rousseau, Daniel Reinharz. Mol Genet Genomic Med 2021
50
Effects of HPV-16 E5, E6 and E7 proteins on survival, adhesion, migration and invasion of trophoblastic cells.
Selma Boulenouar, Christine Weyn, Melody Van Noppen, Mohamed Moussa Ali, Michel Favre, Philippe O Delvenne, Françoise Bex, Agnès Noël, Yvon Englert, Véronique Fontaine. Carcinogenesis 2010
Selma Boulenouar, Christine Weyn, Melody Van Noppen, Mohamed Moussa Ali, Michel Favre, Philippe O Delvenne, Françoise Bex, Agnès Noël, Yvon Englert, Véronique Fontaine. Carcinogenesis 2010
33
33
The association between cervical inflammation and histologic evidence of HPV in PAP smears and adverse pregnancy outcome in low risk population.
Maya Nimrodi, Vered Kleitman, Tamar Wainstock, Ofer Gemer, Michai Meirovitz, Eli Maymon, Neta Benshalom-Tirosh, Offer Erez. Eur J Obstet Gynecol Reprod Biol 2018
Maya Nimrodi, Vered Kleitman, Tamar Wainstock, Ofer Gemer, Michai Meirovitz, Eli Maymon, Neta Benshalom-Tirosh, Offer Erez. Eur J Obstet Gynecol Reprod Biol 2018
33
Editorial: Causes and Consequences of Intrauterine Growth Restriction.
Ivo Bendix, Suzanne L Miller, Elke Winterhager. Front Endocrinol (Lausanne) 2020
Ivo Bendix, Suzanne L Miller, Elke Winterhager. Front Endocrinol (Lausanne) 2020
33
Tumor necrosis factor a-11 and DR15-DQ6 (B*0602) haplotype increase the risk for cervical intraepithelial neoplasia in human papillomavirus 16 seropositive women in Northern Sweden.
M Ghaderi, L Nikitina, C S Peacock, P Hjelmström, G Hallmans, F Wiklund, P Lenner, J M Blackwell, J Dillner, C B Sanjeevi. Cancer Epidemiol Biomarkers Prev 2000
M Ghaderi, L Nikitina, C S Peacock, P Hjelmström, G Hallmans, F Wiklund, P Lenner, J M Blackwell, J Dillner, C B Sanjeevi. Cancer Epidemiol Biomarkers Prev 2000
33
Mucosal and Cutaneous Human Papillomavirus Infections and Cancer Biology.
Tarik Gheit. Front Oncol 2019
Tarik Gheit. Front Oncol 2019
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.