A citation-based method for searching scientific literature

Lena Sagi-Dain, Idit Maya, Adi Reches, Ayala Frumkin, Julia Grinshpun-Cohen, Reeval Segel, Esther Manor, Morad Khayat, Tamar Tenne, Ehud Banne, Adel Shalata, Hagith Yonath, Racheli Berger, Amihood Singer, Shay Ben-Shachar. Obstet Gynecol 2018
Times Cited: 14







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



Times Cited
  Times     Co-cited
Similarity


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
50

Chromosomal microarray vs. NIPS: analysis of 5541 low-risk pregnancies.
Lena Sagi-Dain, Lital Cohen Vig, Sarit Kahana, Shiri Yacobson, Tamar Tenne, Ifat Agmon-Fishman, Cochava Klein, Reut Matar, Lina Basel-Salmon, Idit Maya. Genet Med 2019
31
28

American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants.
Hutton M Kearney, Erik C Thorland, Kerry K Brown, Fabiola Quintero-Rivera, Sarah T South. Genet Med 2011
513
28

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
138
28

Prenatal diagnosis by chromosomal microarray analysis.
Brynn Levy, Ronald Wapner. Fertil Steril 2018
89
28


Microarray analysis in pregnancies with isolated echogenic bowel.
Amihood Singer, Idit Maya, Arie Koifman, Nadra Nasser Samra, Hagit N Baris, Tzipora Falik-Zaccai, Shay Ben Shachar, Lena Sagi-Dain. Early Hum Dev 2018
8
37

Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysis.
S C Hillman, D J McMullan, G Hall, F S Togneri, N James, E J Maher, C H Meller, D Williams, R J Wapner, E R Maher,[...]. Ultrasound Obstet Gynecol 2013
154
21

Prenatal microarray analysis in right aortic arch-a retrospective cohort study and review of the literature.
Idit Maya, Amihood Singer, Hagit N Baris, Yael Goldberg, Adel Shalata, Morad Khayat, Shay Ben-Shachar, Lena Sagi-Dain. J Perinatol 2018
7
28

Microarray analysis in pregnancies with isolated unilateral kidney agenesis.
Lena Sagi-Dain, Idit Maya, Amir Peleg, Adi Reches, Ehud Banne, Hagit N Baris, Tamar Tenne, Amihood Singer, Shay Ben-Shachar. Pediatr Res 2018
6
33

When genotype is not predictive of phenotype: implications for genetic counseling based on 21,594 chromosomal microarray analysis examinations.
Idit Maya, Reuven Sharony, Shiri Yacobson, Sarit Kahana, Josepha Yeshaya, Tamar Tenne, Ifaat Agmon-Fishman, Lital Cohen-Vig, Yael Goldberg, Racheli Berger,[...]. Genet Med 2018
27
14

Rapid prenatal diagnosis using targeted exome sequencing: a cohort study to assess feasibility and potential impact on prenatal counseling and pregnancy management.
Natalie Chandler, Sunayna Best, Jane Hayward, Francesca Faravelli, Sahar Mansour, Emma Kivuva, Dagmar Tapon, Alison Male, Catherine DeVile, Lyn S Chitty. Genet Med 2018
57
14

Association of copy number variants with specific ultrasonographically detected fetal anomalies.
Jennifer C Donnelly, Lawrence D Platt, Andrei Rebarber, Julia Zachary, William A Grobman, Ronald J Wapner. Obstet Gynecol 2014
81
14


ACOG and SMFM guidelines for prenatal diagnosis: Is karyotyping really sufficient?
Sara B Hay, Trilochan Sahoo, Mary K Travis, Karine Hovanes, Natasa Dzidic, Charles Doherty, Michelle N Strecker. Prenat Diagn 2018
31
14

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
14

Meta-analysis of second-trimester markers for trisomy 21.
M Agathokleous, P Chaveeva, L C Y Poon, P Kosinski, K H Nicolaides. Ultrasound Obstet Gynecol 2013
119
14

Amniotic fluid biochemistry in isolated polyhydramnios: a series of 464 cases.
Bichr Allaf, Sophie Dreux, Thomas Schmitz, Isabelle Czerkiewicz, Claudine Le Vaillant, Alexandra Benachi, Véronique Houfflin-Debarge, Martine Maréchaud, Jean-François Oury, Françoise Muller. Prenat Diagn 2015
8
25

Outcomes From Polyhydramnios With Normal Ultrasound.
Enav Yefet, Etty Daniel-Spiegel. Pediatrics 2016
18
14

A review of idiopathic hydramnios and pregnancy outcomes.
Everett F Magann, Suneet P Chauhan, Dorota A Doherty, Monica A Lutgendorf, Marcia I Magann, John C Morrison. Obstet Gynecol Surv 2007
76
14

Etiology and perinatal outcome of polyhydramnios.
M Kollmann, J Voetsch, C Koidl, E Schest, M Haeusler, U Lang, P Klaritsch. Ultraschall Med 2014
12
16

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
14

Chromosomal microarray findings in pregnancies with an isolated pelvic kidney.
Lena Sagi-Dain, Amihood Singer, Ayala Frumkin, Adel Shalata, Arie Koifman, Reeval Segel, Lilach Benyamini, Shlomit Rienstein, Morad Kahyat, Reuven Sharony,[...]. J Perinat Med 2018
2
100


A French Approach to Test Fetuses with Ultrasound Abnormalities Using a Customized Microarray as First-Tier Genetic Test.
Valérie Malan, Jean-Michel Lapierre, Matthieu Egloff, Didier Goidin, Marie-Paule Beaujard, Marie-Laure Maurin, Tania Attié-Bitach, Bettina Bessières, Jean-Pierre Bernard, Philippe Roth,[...]. Cytogenet Genome Res 2015
14
14

Practice guideline: joint CCMG-SOGC recommendations for the use of chromosomal microarray analysis for prenatal diagnosis and assessment of fetal loss in Canada.
Christine M Armour, Shelley Danielle Dougan, Jo-Ann Brock, Radha Chari, Bernie N Chodirker, Isabelle DeBie, Jane A Evans, William T Gibson, Elena Kolomietz, Tanya N Nelson,[...]. J Med Genet 2018
28
14

The clinical use of chromosomal microarray analysis in detection of fetal chromosomal rearrangements: a study from China Mainland.
Yi Wu, Yanlin Wang, Jiong Tao, Xu Han, Xinrong Zhao, Chunmin Liu, Li Gao, Weiwei Cheng. Eur J Obstet Gynecol Reprod Biol 2017
6
33


Birth weight in relation to morbidity and mortality among newborn infants.
D D McIntire, S L Bloom, B M Casey, K J Leveno. N Engl J Med 1999
798
14

Interest of chromosomal microarray analysis in the prenatal diagnosis of fetal intrauterine growth restriction.
Stephanie Brun, Perrine Pennamen, Aurelien Mattuizzi, Frederic Coatleven, Marie Laure Vuillaume, Didier Lacombe, Benoit Arveiler, Jerome Toutain, Caroline Rooryck. Prenat Diagn 2018
4
50

Short-term and long-term sequelae in intrauterine growth retardation (IUGR).
Stefania Longo, Lina Bollani, Lidia Decembrino, Amelia Di Comite, Mauro Angelini, M Stronati. J Matern Fetal Neonatal Med 2013
149
14

Infant neurodevelopment following fetal growth restriction: relationship with antepartum surveillance parameters.
A A Baschat, R M Viscardi, B Hussey-Gardner, N Hashmi, C Harman. Ultrasound Obstet Gynecol 2009
68
14

Major risk factors for stillbirth in high-income countries: a systematic review and meta-analysis.
Vicki Flenady, Laura Koopmans, Philippa Middleton, J Frederik Frøen, Gordon C Smith, Kristen Gibbons, Michael Coory, Adrienne Gordon, David Ellwood, Harold David McIntyre,[...]. Lancet 2011
633
14

Fetal growth restriction and intra-uterine growth restriction: guidelines for clinical practice from the French College of Gynaecologists and Obstetricians.
C Vayssière, L Sentilhes, A Ego, C Bernard, D Cambourieu, C Flamant, G Gascoin, A Gaudineau, G Grangé, V Houfflin-Debarge,[...]. Eur J Obstet Gynecol Reprod Biol 2015
98
14


Fetal growth retardation: associated malformations and chromosomal abnormalities.
R J Snijders, C Sherrod, C M Gosden, K H Nicolaides. Am J Obstet Gynecol 1993
130
14

Genomic Microarray in Fetuses with Early Growth Restriction: A Multicenter Study.
Antoni Borrell, Maribel Grande, Eva Meler, Joan Sabrià, Edurne Mazarico, Anna Muñoz, Laia Rodriguez-Revenga, Cèlia Badenas, Francesc Figueras. Fetal Diagn Ther 2017
11
18

Chromosomal Microarray Analysis in Fetuses with Growth Restriction and Normal Karyotype: A Systematic Review and Meta-Analysis.
Antoni Borrell, Maribel Grande, Montse Pauta, Laia Rodriguez-Revenga, Francesc Figueras. Fetal Diagn Ther 2018
16
14

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
14

Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen).
Erin Rooney Riggs, Erica F Andersen, Athena M Cherry, Sibel Kantarci, Hutton Kearney, Ankita Patel, Gordana Raca, Deborah I Ritter, Sarah T South, Erik C Thorland,[...]. Genet Med 2020
136
14

Changing interpretation of chromosomal microarray over time in a community cohort with intellectual disability.
Emma Palmer, Helen Speirs, Peter J Taylor, Glenda Mullan, Gill Turner, Stewart Einfeld, Bruce Tonge, David Mowat. Am J Med Genet A 2014
30
7


Pierson syndrome: a novel cause of congenital nephrotic syndrome.
Rene' VanDeVoorde, David Witte, Jillene Kogan, Jens Goebel. Pediatrics 2006
22
7

Disorders of fatty acid oxidation and autosomal recessive polycystic kidney disease-different clinical entities and comparable perinatal renal abnormalities.
Agnes Hackl, Katrin Mehler, Ingo Gottschalk, Anne Vierzig, Marcus Eydam, Jan Hauke, Bodo B Beck, Max C Liebau, Regina Ensenauer, Lutz T Weber,[...]. Pediatr Nephrol 2017
12
8

Non-mosaic trisomy 16 in a third-trimester fetus.
M K Yancey, E L Hardin, C Pacheco, C D Kuslich, T A Donlon. Obstet Gynecol 1996
20
7

Serial assessment of amniotic fluid index in uncomplicated term pregnancies: prognostic value of amniotic fluid reduction.
A Locatelli, A Zagarella, L Toso, F Assi, A Ghidini, A Biffi. J Matern Fetal Neonatal Med 2004
21
7


Outcome of singleton pregnancies with severe oligohydramnios in the second and third trimesters.
T D Shipp, B Bromley, S Pauker, F D Frigoletto, B R Benacerraf. Ultrasound Obstet Gynecol 1996
25
7

Prenatal sonographic diagnosis of Majewski syndrome.
Supatra Sirichotiyakul, Theera Tongsong, Chanane Wanapirak, Pharuhas Chanprapaph. J Clin Ultrasound 2002
2
50

Hydrops fetalis, thickened placenta and other sonographic findings in a low-level trisomy 21 mosaicism: a case report.
S Sifakis, O Koukoura, N Mantas, V Velissariou, E Koumantakis. Fetal Diagn Ther 2008
2
50


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.