A citation-based method for searching scientific literature

Francesca Romana Grati, Susan J Gross. Prenat Diagn 2019
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


Clinical validation of a noninvasive prenatal test for genomewide detection of fetal copy number variants.
Roy B Lefkowitz, John A Tynan, Tong Liu, Yijin Wu, Amin R Mazloom, Eyad Almasri, Grant Hogg, Vach Angkachatchai, Chen Zhao, Daniel S Grosu,[...]. Am J Obstet Gynecol 2016
87
50

Origin and clinical relevance of chromosomal aberrations other than the common trisomies detected by genome-wide NIPS: results of the TRIDENT study.
Diane Van Opstal, Merel C van Maarle, Klaske Lichtenbelt, Marjan M Weiss, Heleen Schuring-Blom, Shama L Bhola, Mariette J V Hoffer, Karin Huijsdens-van Amsterdam, Merryn V Macville, Angelique J A Kooper,[...]. Genet Med 2018
40
33

Gestational age and maternal weight effects on fetal cell-free DNA in maternal plasma.
Eric Wang, Annette Batey, Craig Struble, Thomas Musci, Ken Song, Arnold Oliphant. Prenat Diagn 2013
212
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
239
33

22q11.2 deletion syndrome.
Donna M McDonald-McGinn, Kathleen E Sullivan, Bruno Marino, Nicole Philip, Ann Swillen, Jacob A S Vorstman, Elaine H Zackai, Beverly S Emanuel, Joris R Vermeesch, Bernice E Morrow,[...]. Nat Rev Dis Primers 2015
390
33


Validation of a SNP-based non-invasive prenatal test to detect the fetal 22q11.2 deletion in maternal plasma samples.
Harini Ravi, Gabriel McNeill, Shruti Goel, Steven D Meltzer, Nathan Hunkapiller, Allison Ryan, Brynn Levy, Zachary P Demko. PLoS One 2018
14
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
173
33

Noninvasive detection of fetal subchromosome abnormalities via deep sequencing of maternal plasma.
Anupama Srinivasan, Diana W Bianchi, Hui Huang, Amy J Sehnert, Richard P Rava. Am J Hum Genet 2013
170
33

Challenges in non-invasive prenatal screening for sub-chromosomal copy number variations using cell-free DNA.
Henna V Advani, Angela N Barrett, Mark I Evans, Mahesh Choolani. Prenat Diagn 2017
19
33


First Trimester Screening for Common Trisomies and Microdeletion 22q11.2 Syndrome Using Cell-Free DNA: A Prospective Clinical Study.
Karl Oliver Kagan, Markus Hoopmann, Theresa Pfaff, Natalia Prodan, Philipp Wagner, Maximilian Schmid, Andreas Dufke, Ulrike Mau-Holzmann, Sara Brucker, Livia Marcato,[...]. Fetal Diagn Ther 2020
2
100

Non-invasive prenatal diagnosis of fetal aneuploidies using massively parallel sequencing-by-ligation and evidence that cell-free fetal DNA in the maternal plasma originates from cytotrophoblastic cells.
Brigitte H W Faas, Joep de Ligt, Irene Janssen, Alex J Eggink, Lia D E Wijnberger, John M G van Vugt, Lisenka Vissers, Ad Geurts van Kessel. Expert Opin Biol Ther 2012
84
16

Pilot study of a novel multi-functional noninvasive prenatal test on fetus aneuploidy, copy number variation, and single-gene disorder screening.
Yuqin Luo, Bei Jia, Kai Yan, Siping Liu, Xiaojie Song, Mingfa Chen, Fan Jin, Yang Du, Juan Wang, Yan Hong,[...]. Mol Genet Genomic Med 2019
12
16

Noninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy management.
Baran Bayindir, Luc Dehaspe, Nathalie Brison, Paul Brady, Simon Ardui, Molka Kammoun, Lars Van der Veken, Klaske Lichtenbelt, Kris Van den Bogaert, Jeroen Van Houdt,[...]. Eur J Hum Genet 2015
64
16

Determination of fetal DNA fraction from the plasma of pregnant women using sequence read counts.
Sung K Kim, Gregory Hannum, Jennifer Geis, John Tynan, Grant Hogg, Chen Zhao, Taylor J Jensen, Amin R Mazloom, Paul Oeth, Mathias Ehrich,[...]. Prenat Diagn 2015
104
16

CNV-WebStore: online CNV analysis, storage and interpretation.
Geert Vandeweyer, Edwin Reyniers, Wim Wuyts, Liesbeth Rooms, R Frank Kooy. BMC Bioinformatics 2011
50
16

The 13q-deletion syndrome.
P W Allderdice, J G Davis, O J Miller, H P Klinger, D Warburton, D A Miller, F H Allen, C A Abrams, E McGilvray. Am J Hum Genet 1969
155
16

Genome-wide cfDNA screening: clinical laboratory experience with the first 10,000 cases.
Mathias Ehrich, John Tynan, Amin Mazloom, Eyad Almasri, Ron McCullough, Theresa Boomer, Daniel Grosu, Jason Chibuk. Genet Med 2017
38
16

Chromosome 13q deletion syndrome involving 13q31‑qter: A case report.
Yue-Ping Wang, Da-Jia Wang, Zhi-Bin Niu, Wan-Ting Cui. Mol Med Rep 2017
12
16

Predicting fetoplacental chromosomal mosaicism during non-invasive prenatal testing.
Nathalie Brison, Maria Neofytou, Luc Dehaspe, Baran Bayindir, Kris Van Den Bogaert, Leila Dardour, Hilde Peeters, Hilde Van Esch, Griet Van Buggenhout, Annick Vogels,[...]. Prenat Diagn 2018
29
16

Clinical utility of non-invasive prenatal testing in pregnancies with ultrasound anomalies.
L Beulen, B H W Faas, I Feenstra, J M G van Vugt, M N Bekker. Ultrasound Obstet Gynecol 2017
32
16

13q Deletion and central nervous system anomalies: further insights from karyotype-phenotype analyses of 14 patients.
Lucia Ballarati, Elena Rossi, Maria Teresa Bonati, Stefania Gimelli, Paola Maraschio, Palma Finelli, Sabrina Giglio, Elisabetta Lapi, Maria Francesca Bedeschi, Silvana Guerneri,[...]. J Med Genet 2007
90
16

Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired.
S A Brown, D Warburton, L Y Brown, C Y Yu, E R Roeder, S Stengel-Rutkowski, R C Hennekam, M Muenke. Nat Genet 1998
365
16

Cell-Free DNA Testing for Fetal Chromosomal Anomalies in clinical practice: Austrian-German-Swiss Recommendations for non-invasive prenatal tests (NIPT).
M Schmid, P Klaritsch, W Arzt, T Burkhardt, H C Duba, M Häusler, E Hafner, U Lang, B Pertl, M Speicher,[...]. Ultraschall Med 2015
17
16

The thymic-thoracic ratio in fetal heart defects: a simple way to identify fetuses at high risk for microdeletion 22q11.
R Chaoui, K-S Heling, A Sarut Lopez, G Thiel, K Karl. Ultrasound Obstet Gynecol 2011
47
16

A French collaborative survey of 272 fetuses with 22q11.2 deletion: ultrasound findings, fetal autopsies and pregnancy outcomes.
J Besseau-Ayasse, C Violle-Poirsier, A Bazin, N Gruchy, A Moncla, F Girard, M Till, F Mugneret, A Coussement, F Pelluard,[...]. Prenat Diagn 2014
33
16


Genotype-phenotype correlation in 22q11.2 deletion syndrome.
Elena Michaelovsky, Amos Frisch, Miri Carmel, Miriam Patya, Omer Zarchi, Tamar Green, Lina Basel-Vanagaite, Abraham Weizman, Doron Gothelf. BMC Med Genet 2012
62
16


All-cause mortality and survival in adults with 22q11.2 deletion syndrome.
Lily Van, Tracy Heung, Justin Graffi, Enoch Ng, Sarah Malecki, Spencer Van Mil, Erik Boot, Maria Corral, Eva W C Chow, Kathleen A Hodgkinson,[...]. Genet Med 2019
11
16

Association of airway abnormalities with 22q11.2 deletion syndrome.
Rosalba Sacca, Karen B Zur, T Blaine Crowley, Elaine H Zackai, Kathleen D Valverde, Donna M McDonald-McGinn. Int J Pediatr Otorhinolaryngol 2017
20
16

Neonatal Tracheostomy.
Jonathan Walsh, Jeffrey Rastatter. Clin Perinatol 2018
4
25

Dysphagia in children with a 22q11.2 deletion: unusual pattern found on modified barium swallow.
P S Eicher, D M McDonald-Mcginn, C A Fox, D A Driscoll, B S Emanuel, E H Zackai. J Pediatr 2000
67
16

Fetuses with right aortic arch: a multicenter cohort study and meta-analysis.
F D'Antonio, A Khalil, V Zidere, J S Carvalho. Ultrasound Obstet Gynecol 2016
41
16

Aortic arch anomalies associated with chromosome 22q11 deletion (CATCH 22).
K Momma, R Matsuoka, A Takao. Pediatr Cardiol 1999
94
16

Testing for 22q11 microdeletion in 146 fetuses with nuchal translucency above the 99th percentile and a normal karyotype.
Charlotte Kvist Lautrup, Susanne Kjaergaard, Karen Brøndum-Nielsen, Christina Fagerberg, Jens Michael Hertz, Olav Bennikke Bjørn Petersen, Mette Warming Jørgensen, Ida Vogel. Acta Obstet Gynecol Scand 2008
12
16

Obesity and cell-free DNA "no calls": is there an optimal gestational age at time of sampling?
Mary C Livergood, Kay A LeChien, Amanda S Trudell. Am J Obstet Gynecol 2017
34
16

Combining the use of a fetal fraction-based risk algorithm and probability of an informative redraw in noninvasive prenatal testing for fetal aneuploidy.
Peter Benn, Kimberly Martin, Trudy McKanna, Elizabeth Valenti, Paul Billings, Zachary Demko. J Genet Couns 2020
2
50

Prenatal Screening for 22q11.2 Deletion Using a Targeted Microarray-Based Cell-Free DNA Test.
Maximilian Schmid, Eric Wang, Patrick E Bogard, Elisa Bevilacqua, Coleen Hacker, Susie Wang, Jigna Doshi, Karen White, Jennifer Kaplan, Andrew Sparks,[...]. Fetal Diagn Ther 2018
8
16

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
301
16

Fetal fraction-based risk algorithm for non-invasive prenatal testing: screening for trisomies 13 and 18 and triploidy in women with low cell-free fetal DNA.
T McKanna, A Ryan, S Krinshpun, S Kareht, K Marchand, C Grabarits, M Ali, A McElheny, K Gardiner, K LeChien,[...]. Ultrasound Obstet Gynecol 2019
17
16

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
646
16

Noninvasive prenatal screening at low fetal fraction: comparing whole-genome sequencing and single-nucleotide polymorphism methods.
Carlo G Artieri, Carrie Haverty, Eric A Evans, James D Goldberg, Imran S Haque, Yuval Yaron, Dale Muzzey. Prenat Diagn 2017
21
16


Fetal fraction evaluation in non-invasive prenatal screening (NIPS).
Matthew S Hestand, Mark Bessem, Peter van Rijn, Renee X de Menezes, Daoud Sie, Ingrid Bakker, Elles M J Boon, Erik A Sistermans, Marjan M Weiss. Eur J Hum Genet 2019
15
16

Second generation noninvasive fetal genome analysis reveals de novo mutations, single-base parental inheritance, and preferred DNA ends.
K C Allen Chan, Peiyong Jiang, Kun Sun, Yvonne K Y Cheng, Yu K Tong, Suk Hang Cheng, Ada I C Wong, Irena Hudecova, Tak Y Leung, Rossa W K Chiu,[...]. Proc Natl Acad Sci U S A 2016
73
16

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
53
16

Fetal cell-free DNA fraction in maternal plasma is affected by fetal trisomy.
Nobuhiro Suzumori, Takeshi Ebara, Takahiro Yamada, Osamu Samura, Junko Yotsumoto, Miyuki Nishiyama, Kiyonori Miura, Hideaki Sawai, Jun Murotsuki, Michihiro Kitagawa,[...]. J Hum Genet 2016
32
16


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.