A citation-based method for searching scientific literature

Myra C B van Zwieten, Dick L Willems, Liesbeth L Litjens, Heleen G Schuring-Blom, Nico Leschot. Eur J Obstet Gynecol Reprod Biol 2005
Times Cited: 19







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



Times Cited
  Times     Co-cited
Similarity


Rapid, high throughput prenatal detection of aneuploidy using a novel quantitative method (MLPA).
H R Slater, D L Bruno, H Ren, M Pertile, J P Schouten, K H A Choo. J Med Genet 2003
98
21

Evaluation of molecular tests for prenatal diagnosis of chromosome abnormalities.
G M Grimshaw, A Szczepura, M Hultén, F MacDonald, N C Nevin, F Sutton, S Dhanjal. Health Technol Assess 2003
52
21

The diagnostic performance of cytogenetic investigation in amniotic fluid cells and chorionic villi.
F J Los, C van Den Berg, H I Wildschut, H Brandenburg, N S den Hollander, E M Schoonderwaldt, L Pijpers, R Jan H Galjaard, D Van Opstal. Prenat Diagn 2001
17
23


Rapid aneuploidy detection with multiplex ligation-dependent probe amplification: a prospective study of 4000 amniotic fluid samples.
Diane Van Opstal, Marjan Boter, Danielle de Jong, Cardi van den Berg, Hennie T Brüggenwirth, Hajo I J Wildschut, Annelies de Klein, Robert-Jan H Galjaard. Eur J Hum Genet 2009
50
21

Multiplex ligation-dependent probe amplification (MLPA) as a stand-alone test for rapid aneuploidy detection in amniotic fluid cells.
Angelique J A Kooper, Brigitte H W Faas, Ellen Kater-Baats, Ton Feuth, Jasper C J A Janssen, Ineke van der Burgt, Fred K Lotgering, Ad Geurts van Kessel, Arie P T Smits. Prenat Diagn 2008
21
21


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
21

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
21


Outcomes of pregnancies diagnosed with Klinefelter syndrome: the possible influence of health professionals.
Theresa M Marteau, Irma Nippert, Sue Hall, Caroline Limbert, Margaret Reid, Martin Bobrow, Alan Cameron, Martina Cornel, Mariet van Diem, Bernd Eiben,[...]. Prenat Diagn 2002
43
15


Rapid detection of chromosomal aneuploidies in uncultured amniocytes by multiplex ligation-dependent probe amplification (MLPA).
R Hochstenbach, J Meijer, J van de Brug, I Vossebeld-Hoff, R Jansen, R B van der Luijt, R J Sinke, G C M L Page-Christiaens, J-K Ploos van Amstel, J M de Pater. Prenat Diagn 2005
52
15

Computer-assisted prenatal aneuploidy screening for chromosome 13, 18, 21, X and Y based on multiplex ligation-dependent probe amplification (MLPA).
Tommy Gerdes, Maria Kirchhoff, Anne-Marie Lind, Gitte Vestergaard Larsen, Marianne Schwartz, Claes Lundsteen. Eur J Hum Genet 2005
48
15

Molecular cytogenetic and rapid aneuploidy detection methods in prenatal diagnosis.
Lisa G Shaffer, The-Hung Bui. Am J Med Genet C Semin Med Genet 2007
81
15

Rapid prenatal diagnosis of aneuploidy using quantitative fluorescence-PCR (QF-PCR).
Caroline Mackie Ogilvie, Celia Donaghue, Susan P Fox, Zoe Docherty, Kathy Mann. J Histochem Cytochem 2005
50
15


Randomised controlled trial of genetic amniocentesis in 4606 low-risk women.
A Tabor, J Philip, M Madsen, J Bang, E B Obel, B Nørgaard-Pedersen. Lancet 1986
590
15

Prenatal cytogenetic diagnosis: gone FISHing, BAC soon!
T-H Bui. Ultrasound Obstet Gynecol 2007
23
15

Genetic counseling for sex chromosome abnormalities.
Mary G Linden, Bruce G Bender, Arthur Robinson. Am J Med Genet 2002
48
15

Sex chromosome trisomies in Europe: prevalence, prenatal detection and outcome of pregnancy.
Patricia Anne Boyd, Maria Loane, Ester Garne, Babak Khoshnood, Helen Dolk. Eur J Hum Genet 2011
44
15

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
15

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
15


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
15

Incidental prenatal diagnosis of sex chromosome aneuploidies: health, behavior, and fertility.
J J P M Pieters, A J A Kooper, A Geurts van Kessel, D D M Braat, A P T Smits. ISRN Obstet Gynecol 2011
24
15

Non-targeted whole genome 250K SNP array analysis as replacement for karyotyping in fetuses with structural ultrasound anomalies: evaluation of a one-year experience.
Brigitte H W Faas, Ilse Feenstra, Alex J Eggink, Angelique J A Kooper, Rolph Pfundt, John M G van Vugt, Nicole de Leeuw. Prenat Diagn 2012
31
15

Application of SNP array for rapid prenatal diagnosis: implementation, genetic counselling and diagnostic flow.
Malgorzata Srebniak, Marjan Boter, Grétel Oudesluijs, Marieke Joosten, Lutgarde Govaerts, Diane Van Opstal, Robert-Jan H Galjaard. Eur J Hum Genet 2011
74
15

The introduction of arrays in prenatal diagnosis: a special challenge.
Annalisa Vetro, Katelijne Bouman, Ros Hastings, Dominic J McMullan, Joris R Vermeesch, Konstantin Miller, Birgit Sikkema-Raddatz, David H Ledbetter, Orsetta Zuffardi, Conny M A van Ravenswaaij-Arts. Hum Mutat 2012
51
15

Array technology in prenatal diagnosis.
Orsetta Zuffardi, Annalisa Vetro, Paul Brady, Joris Vermeesch. Semin Fetal Neonatal Med 2011
19
15

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
15

Women's experiences receiving abnormal prenatal chromosomal microarray testing results.
Barbara A Bernhardt, Danielle Soucier, Karen Hanson, Melissa S Savage, Laird Jackson, Ronald J Wapner. Genet Med 2013
129
15

Prenatal diagnosis and management of sex chromosome aneuploidy: a report on 98 cases.
Jean-Luc Brun, Flore Gangbo, Zon Qi Wen, Katia Galant, Laurence Taine, Brigitte Maugey-Laulom, Denis Roux, Raphaelle Mangione, Jacques Horovitz, Robert Saura. Prenat Diagn 2004
33
10


Factors influencing parental decision making in prenatal diagnosis of sex chromosome aneuploidy.
Gábor Mezei, Csaba Papp, Ernö Tóth-Pál, Artúr Beke, Zoltán Papp. Obstet Gynecol 2004
41
10

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
253
10






Rapid aneuploidy screening (FISH or QF-PCR): the changing scene in prenatal diagnosis?
W C Leung, Elizabeth T Lau, Terence T Lao, Mary H Y Tang. Expert Rev Mol Diagn 2004
19
10

Multiplex ligation-dependent probe amplification versus karyotyping in prenatal diagnosis: the M.A.K.E. study.
Elisabeth M A Boormans, Erwin Birnie, Hajo I Wildschut, Heleen G Schuring-Blom, Dick Oepkes, Carla A C van Oppen, Jan G Nijhuis, Merryn V E Macville, Angelique J A Kooper, Karin Huijsdens,[...]. BMC Pregnancy Childbirth 2008
17
11

Comparative genomic hybridization and prenatal diagnosis.
Ignatia B Van den Veyver, Arthur L Beaudet. Curr Opin Obstet Gynecol 2006
38
10

Prenatal genetic diagnosis in 3000 amniocenteses.
M S Golbus, W D Loughman, C J Epstein, G Halbasch, J D Stephens, B D Hall. N Engl J Med 1979
273
10

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
10

Karyotyping or rapid aneuploidy detection in prenatal diagnosis? The different views of users and providers of prenatal care.
E M A Boormans, E Birnie, C M Bilardo, D Oepkes, G J Bonsel, J M M van Lith. BJOG 2009
12
16

Reproduction in men with Klinefelter syndrome: the past, the present, and the future.
Darius A Paduch, Alexander Bolyakov, Paula Cohen, Alexander Travis. Semin Reprod Med 2009
48
10

Rethinking autonomy in the context of prenatal screening decision-making.
Elisa García, Danielle R M Timmermans, Evert van Leeuwen. Prenat Diagn 2008
42
10



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.