A citation-based method for searching scientific literature

Isabel Filges, Anjeung Kang, Vanessa Klug, Friedel Wenzel, Karl Heinimann, Sevgi Tercanli, Peter Miny. Prenat Diagn 2011
Times Cited: 15







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



Times Cited
  Times     Co-cited
Similarity


Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein,[...]. Am J Hum Genet 2010
33

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
33

Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysis.
S C Hillman, S Pretlove, A Coomarasamy, D J McMullan, E V Davison, E R Maher, M D Kilby. Ultrasound Obstet Gynecol 2011
154
26

Current controversies in prenatal diagnosis 3: is conventional chromosome analysis necessary in the post-array CGH era?
The-Hung Bui, Annalisa Vetro, Orsetta Zuffardi, Lisa G Shaffer. Prenat Diagn 2011
39
26


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
26


Cytogenetic results from the U.S. Collaborative Study on CVS.
D H Ledbetter, J M Zachary, J L Simpson, M S Golbus, E Pergament, L Jackson, M J Mahoney, R J Desnick, J Schulman, K L Copeland. Prenat Diagn 1992
271
26

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
20


High resolution array analysis: diagnosing pregnancies with abnormal ultrasound findings.
M Tyreman, K M Abbott, L R Willatt, R Nash, C Lees, J Whittaker, I Simonic. J Med Genet 2009
90
20

Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization.
Trilochan Sahoo, Sau Wai Cheung, Patricia Ward, Sandra Darilek, Ankita Patel, Daniela del Gaudio, Sung Hae L Kang, Seema R Lalani, Jiangzhen Li, Sallie McAdoo,[...]. Genet Med 2006
122
20

Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases.
Ignatia B Van den Veyver, Ankita Patel, Chad A Shaw, Amber N Pursley, Sung-Hae L Kang, Marcia J Simovich, Patricia A Ward, Sandra Darilek, Anthony Johnson, Sarah E Neill,[...]. Prenat Diagn 2009
139
20

Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study.
Rossa W K Chiu, Ranjit Akolekar, Yama W L Zheng, Tak Y Leung, Hao Sun, K C Allen Chan, Fiona M F Lun, Attie T J I Go, Elizabeth T Lau, William W K To,[...]. BMJ 2011
473
20


Identification of submicroscopic chromosomal aberrations in fetuses with increased nuchal translucency and apparently normal karyotype.
T Y Leung, I Vogel, T K Lau, W Chong, J A Hyett, O B Petersen, K W Choy. Ultrasound Obstet Gynecol 2011
80
20

Introducing array comparative genomic hybridization into routine prenatal diagnosis practice: a prospective study on over 1000 consecutive clinical cases.
Francesco Fiorentino, Fiorina Caiazzo, Stefania Napolitano, Letizia Spizzichino, Sara Bono, Mariateresa Sessa, Andrea Nuccitelli, Anil Biricik, Anthony Gordon, Giuseppe Rizzo,[...]. Prenat Diagn 2011
75
20

Reevaluating confined placental mosaicism.
Gail Stetten, Cathleen S Escallon, Sarah T South, Joseph L McMichael, Daniel O Saul, Karin J Blakemore. Am J Med Genet A 2004
36
20


Confined placental mosaicism: implications for fetal chromosomal analysis using microarray comparative genomic hybridization.
Evangelia Karampetsou, Deborah Morrogh, Terry Ballard, Jonathan J Waters, Nicholas Lench, Lyn S Chitty. Prenat Diagn 2014
12
25

Complete discrepancy between QF-PCR analysis of uncultured villi and karyotyping of cultured cells in the prenatal diagnosis of trisomy 21 in three CVS.
Jonathan J Waters, Kathy Mann, Lee Grimsley, Caroline Mackie Ogilvie, Celia Donaghue, Leonie Staples, Alison Hills, Tracey Adams, Christine Wilson. Prenat Diagn 2007
32
13

Diagnostic utility of array-based comparative genomic hybridization (aCGH) in a prenatal setting.
Idit Maya, Bella Davidov, Liron Gershovitz, Yael Zalzstein, Ellen Taub, Justine Coppinger, Lisa G Shaffer, Mordechai Shohat. Prenat Diagn 2010
63
13

Fetal-specific DNA methylation ratio permits noninvasive prenatal diagnosis of trisomy 21.
Elisavet A Papageorgiou, Alex Karagrigoriou, Evdokia Tsaliki, Voula Velissariou, Nigel P Carter, Philippos C Patsalis. Nat Med 2011
126
13

The outcome of pregnancies with confined placental chromosome mosaicism in cytotrophoblast cells.
N J Leschot, G H Schuring-Blom, A C Van Prooijen-Knegt, M Verjaal, K Hansson, H Wolf, H H Kanhai, J M Van Vugt, G C Christiaens. Prenat Diagn 1996
24
13

Detection of low-level mosaicism by array CGH in routine diagnostic specimens.
Blake C Ballif, Emily A Rorem, Kyle Sundin, Matt Lincicum, Shannon Gaskin, Justine Coppinger, Catherine D Kashork, Lisa G Shaffer, Bassem A Bejjani. Am J Med Genet A 2006
207
13



Detection of fetal trisomies 21 and 18 from maternal blood using triple gradient and magnetic cell sorting.
D Gänshirt-Ahlert, R Börjesson-Stoll, M Burschyk, A Dohr, H S Garritsen, E Helmer, P Miny, M Velasco, C Walde, D Patterson. Am J Reprod Immunol 1993
175
13

Detection of fetal cells with 47,XY,+21 karyotype in maternal peripheral blood.
D W Bianchi, A Mahr, G K Zickwolf, T W Houseal, A F Flint, K W Klinger. Hum Genet 1992
110
13

The detection of chromosome anomalies by QF-PCR and residual risks as compared to G-banded analysis.
Marsha D Speevak, Jean McGowan-Jordan, Kathy Chun. Prenat Diagn 2011
13
15

Microarray-based CGH detects chromosomal mosaicism not revealed by conventional cytogenetics.
Sau W Cheung, Chad A Shaw, Daryl A Scott, Ankita Patel, Trilochan Sahoo, Carlos A Bacino, Amber Pursley, Jiangzhen Li, Robert Erickson, Andrea L Gropman,[...]. Am J Med Genet A 2007
129
13

Trends in the utilization of invasive prenatal diagnosis in The Netherlands during 2000-2009.
Klaske D Lichtenbelt, Behrooz Z Alizadeh, Peter G Scheffer, Philip Stoutenbeek, Peter C J I Schielen, Lieve C M L Page-Christiaens, G Heleen Schuring-Blom. Prenat Diagn 2011
23
13



The predictive value of cytogenetic diagnosis after CVS based on 4860 cases with both direct and culture methods.
M C Pittalis, L Dalprà, F Torricelli, N Rizzo, G Nocera, E Cariati, L Santarini, M G Tibiletti, S Agosti, L Bovicelli. Prenat Diagn 1994
54
13

Efficient direct chromosome analyses and enzyme determinations from chorionic villi samples in the first trimester of pregnancy.
G Simoni, B Brambati, C Danesino, F Rossella, G L Terzoli, M Ferrari, M Fraccaro. Hum Genet 1983
445
13

Incidence and significance of chromosome mosaicism involving an autosomal structural abnormality diagnosed prenatally through amniocentesis: a collaborative study.
L Y Hsu, M T Yu, K E Richkind, D L Van Dyke, B F Crandall, D F Saxe, G S Khodr, M Mennuti, G Stetten, W A Miller,[...]. Prenat Diagn 1996
78
13

Detection of low-level mosaicism and placental mosaicism by oligonucleotide array comparative genomic hybridization.
Stuart A Scott, Ninette Cohen, Tracy Brandt, Gokce Toruner, Robert J Desnick, Lisa Edelmann. Genet Med 2010
63
13

Fetal gender and aneuploidy detection using fetal cells in maternal blood: analysis of NIFTY I data. National Institute of Child Health and Development Fetal Cell Isolation Study.
D W Bianchi, J L Simpson, L G Jackson, S Elias, W Holzgreve, M I Evans, K A Dukes, L M Sullivan, K W Klinger, F Z Bischoff,[...]. Prenat Diagn 2002
193
13

Fetal cells in the blood of pregnant women: detection and enrichment by fluorescence-activated cell sorting.
L A Herzenberg, D W Bianchi, J Schröder, H M Cann, G M Iverson. Proc Natl Acad Sci U S A 1979
343
13

Georg Schmorl on trophoblasts in the maternal circulation.
O Lapaire, W Holzgreve, J C Oosterwijk, R Brinkhaus, D W Bianchi. Placenta 2007
66
13

Copy number variations and clinical cytogenetic diagnosis of constitutional disorders.
Charles Lee, A John Iafrate, Arthur R Brothman. Nat Genet 2007
270
13


Impact of a new national screening policy for Down's syndrome in Denmark: population based cohort study.
Charlotte K Ekelund, Finn Stener Jørgensen, Olav Bjørn Petersen, Karin Sundberg, Ann Tabor. BMJ 2008
149
13

Array comparative genomic hybridization in prenatal diagnosis: another experience.
F Vialard, D Molina Gomes, B Leroy, E Quarello, A Escalona, C Le Sciellour, V Serazin, J Roume, Y Ville, P de Mazancourt,[...]. Fetal Diagn Ther 2009
58
13

Maternal plasma DNA sequencing reveals the genome-wide genetic and mutational profile of the fetus.
Y M Dennis Lo, K C Allen Chan, Hao Sun, Eric Z Chen, Peiyong Jiang, Fiona M F Lun, Yama W Zheng, Tak Y Leung, Tze K Lau, Charles R Cantor,[...]. Sci Transl Med 2010
567
13

Use of array comparative genomic hybridization for prenatal diagnosis of fetuses with sonographic anomalies and normal metaphase karyotype.
Linda Kleeman, Diana W Bianchi, Lisa G Shaffer, Emily Rorem, Janet Cowan, Sabrina D Craigo, Hocine Tighiouart, Louise E Wilkins-Haug. Prenat Diagn 2009
78
13

Genetic counselling and ethical issues with chromosome microarray analysis in prenatal testing.
George McGillivray, Jill A Rosenfeld, R J McKinlay Gardner, Lynn H Gillam. Prenat Diagn 2012
68
13

Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011.
A Novelli, F R Grati, L Ballarati, L Bernardini, D Bizzoco, L Camurri, R Casalone, L Cardarelli, P Cavalli, R Ciccone,[...]. Ultrasound Obstet Gynecol 2012
44
13

Fetal aneuploidy screening by maternal plasma DNA sequencing: 'false positive' due to confined placental mosaicism.
H Choi, T K Lau, F M Jiang, M K Chan, H Y Zhang, P S S Lo, F Chen, L Zhang, W Wang. Prenat Diagn 2013
70
13


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.