A citation-based method for searching scientific literature

H Daum, A Ben David, M Nadjari, S Zenvirt, S Helman, N Yanai, V Meiner, S Yagel, A Frumkin, S Shkedi Rafid. Ultrasound Obstet Gynecol 2019
Times Cited: 7







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



Times Cited
  Times     Co-cited
Similarity


Offering pregnant women different levels of genetic information from prenatal chromosome microarray: a prospective study.
Jane L Halliday, Cecile Muller, Taryn Charles, Fiona Norris, Joanne Kennedy, Sharon Lewis, Bettina Meiser, Susan Donath, Zornitza Stark, George McGillivray,[...]. Eur J Hum Genet 2018
11
42

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
28

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
28

The use of chromosomal microarray for prenatal diagnosis.
Lorraine Dugoff, Mary E Norton, Jeffrey A Kuller. Am J Obstet Gynecol 2016
62
28

Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challenges.
Olivier Vanakker, Catheline Vilain, Katrien Janssens, Nathalie Van der Aa, Guillaume Smits, Claude Bandelier, Bettina Blaumeiser, Saskia Bulk, Jean-Hubert Caberg, Anne De Leener,[...]. Eur J Med Genet 2014
61
28


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
28

The Psychological Impact of Prenatal Diagnosis and Disclosure of Susceptibility Loci: First Impressions of Parents' Experiences.
S L van der Steen, S R Riedijk, J Verhagen-Visser, L C P Govaerts, M I Srebniak, D Van Opstal, M Joosten, M F C M Knapen, A Tibben, K E M Diderich,[...]. J Genet Couns 2016
26
28

Pregnant couples at increased risk for common aneuploidies choose maximal information from invasive genetic testing.
S L van der Steen, K E M Diderich, S R Riedijk, J Verhagen-Visser, L C P Govaerts, M Joosten, M F C M Knapen, D Van Opstal, M I Srebniak, A Tibben,[...]. Clin Genet 2015
32
28

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

What results to disclose, when, and who decides? Healthcare professionals' views on prenatal chromosomal microarray analysis.
Shiri Shkedi-Rafid, Angela Fenwick, Sandi Dheensa, Diana Wellesley, Anneke M Lucassen. Prenat Diagn 2016
20
28


Outcomes From Polyhydramnios With Normal Ultrasound.
Enav Yefet, Etty Daniel-Spiegel. Pediatrics 2016
18
28

Procedure-related risk of miscarriage following amniocentesis and chorionic villus sampling: a systematic review and meta-analysis.
R Akolekar, J Beta, G Picciarelli, C Ogilvie, F D'Antonio. Ultrasound Obstet Gynecol 2015
320
28

The yield and complications of amniocentesis performed after 24 weeks of gestation.
Keren Tzadikevitch Geffen, Ohad Ben-Zvi, Omer Weitzner, Amir Peleg, Tal Biron-Shental, Rivka Sukenik-Halevy. Arch Gynecol Obstet 2017
3
66

Pregnancy outcome after third trimester amniocentesis: a single center experience.
Rinat Gabbay-Benziv, Yariv Yogev, Nir Melamed, Avi Ben-Haroush, Israel Meizner, Joseph Pardo. J Matern Fetal Neonatal Med 2012
11
28

Information Women Choose to Receive About Prenatal Chromosomal Microarray Analysis.
Hagit Hochner, Hagit Daum, Liza Douiev, Naama Zvi, Ayala Frumkin, Michal Macarov, Adva Kimchi-Shaal, Nuphar Hacohen, Avital Eilat, Duha Faham,[...]. Obstet Gynecol 2020
6
33

Universal chromosomal microarray analysis reveals high proportion of copy-number variants in low-risk pregnancies.
S Stern, N Hacohen, V Meiner, S Yagel, S Zenvirt, S Shkedi-Rafid, M Macarov, D V Valsky, S Porat, N Yanai,[...]. Ultrasound Obstet Gynecol 2021
8
28

Noninvasive whole-genome sequencing of a human fetus.
Jacob O Kitzman, Matthew W Snyder, Mario Ventura, Alexandra P Lewis, Ruolan Qiu, Lavone E Simmons, Hilary S Gammill, Craig E Rubens, Donna A Santillan, Jeffrey C Murray,[...]. Sci Transl Med 2012
240
14

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
14


Microarray-based cell-free DNA analysis improves noninvasive prenatal testing.
Kara Juneau, Patrick E Bogard, Stephanie Huang, Morassa Mohseni, Eric T Wang, Paul Ryvkin, Christopher Kingsley, Craig A Struble, Arnold Oliphant, Jacob M Zahn. Fetal Diagn Ther 2014
47
14


"If it helps..." the use of microarray technology in prenatal testing: patient and partners reflections.
Sarah C Hillman, John Skelton, Elizabeth Quinlan-Jones, Amie Wilson, Mark D Kilby. Am J Med Genet A 2013
26
14

Should pretest genetic counselling be required for patients pursuing genomic sequencing? Results from a survey of participants in a large genomic implementation study.
Joel E Pacyna, Carmen Radecki Breitkopf, Sarah M Jenkins, Erica J Sutton, Caroline Horrow, Iftikhar J Kullo, Richard R Sharp. J Med Genet 2019
13
14

Frequency of submicroscopic chromosomal aberrations in pregnancies without increased risk for structural chromosomal aberrations: systematic review and meta-analysis.
M I Srebniak, M Joosten, M F C M Knapen, L R Arends, M Polak, S van Veen, A T J I Go, D Van Opstal. Ultrasound Obstet Gynecol 2018
40
14

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
14

Prenatal diagnostic testing of the Noonan syndrome genes in fetuses with abnormal ultrasound findings.
Ellen A Croonen, Willy M Nillesen, Kyra E Stuurman, Gretel Oudesluijs, Ingrid M B M van de Laar, Liesbeth Martens, Charlotte Ockeloen, Inge B Mathijssen, Marga Schepens, Martina Ruiterkamp-Versteeg,[...]. Eur J Hum Genet 2013
47
14

Overview of the impact of noninvasive prenatal testing on diagnostic procedures.
Steven L Warsof, Sebastian Larion, Alfred Z Abuhamad. Prenat Diagn 2015
75
14

Utilization of noninvasive prenatal testing: impact on referrals for diagnostic testing.
John Williams, Steve Rad, Sarah Beauchamp, Dalar Ratousi, Vaishnavi Subramaniam, Sayeh Farivar, Margareta D Pisarska. Am J Obstet Gynecol 2015
50
14

Polyhydramnios, fetal overgrowth, and macrocephaly: prenatal ultrasound findings of Costello syndrome.
Laura P Smith, John Podraza, Virginia K Proud. Am J Med Genet A 2009
29
14

Respiratory system involvement in Costello syndrome.
Natalia Gomez-Ospina, Christin Kuo, Amitha Lakshmi Ananth, Angela Myers, Marie-Luise Brennan, David A Stevenson, Jonathan A Bernstein, Louanne Hudgins. Am J Med Genet A 2016
5
20


Idiopathic polyhydramnios and postnatal findings.
Desirée M J Dorleijn, Titia E Cohen-Overbeek, Floris Groenendaal, Hein W Bruinse, Philip Stoutenbeek. J Matern Fetal Neonatal Med 2009
27
14

Prenatal ultrasound factors and genetic disorders in pregnancies complicated by polyhydramnios.
Simona Boito, Francesca Crovetto, Benedetta Ischia, Beatrice Letizia Crippa, Isabella Fabietti, Maria Francesca Bedeschi, Faustina Lalatta, Lorenzo Colombo, Fabio Mosca, Luigi Fedele,[...]. Prenat Diagn 2016
6
16

Retrospective study of prenatal ultrasound findings in newborns with a Noonan spectrum disorder.
Fahad Hakami, Mitchell W Dillon, Matthew Lebo, Heather Mason-Suares. Prenat Diagn 2016
13
14

Risk of chromosomal abnormalities in patients with idiopathic polyhydramnios.
K Brady, W J Polzin, J N Kopelman, J A Read. Obstet Gynecol 1992
48
14

Maximal amniotic fluid index as a prognostic factor in pregnancies complicated by polyhydramnios.
S Pri-Paz, N Khalek, K M Fuchs, L L Simpson. Ultrasound Obstet Gynecol 2012
40
14

Polyhydramnios: a review.
M S Cardwell. Obstet Gynecol Surv 1987
29
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

Perinatal features of the RASopathies: Noonan syndrome, cardiofaciocutaneous syndrome and Costello syndrome.
Angela Myers, Jonathan A Bernstein, Marie-Luise Brennan, Cynthia Curry, Edward D Esplin, Jamie Fisher, Margaret Homeyer, Melanie A Manning, Eric A Muller, Anna-Kaisa Niemi,[...]. Am J Med Genet A 2014
40
14

Spontaneous mutation and parental age in humans.
N Risch, E W Reich, M M Wishnick, J G McCarthy. Am J Hum Genet 1987
170
14

Polyhydramnios: ultrasonically detected prevalence and neonatal outcome.
L M Hill, R Breckle, M L Thomas, J K Fries. Obstet Gynecol 1987
111
14

The RASopathies.
Katherine A Rauen. Annu Rev Genomics Hum Genet 2013
392
14


Maternal and fetal capillary malformation-arteriovenous malformation (CM-AVM) due to a novel RASA1 mutation presenting with prenatal non-immune hydrops fetalis.
Rachael T Overcash, Christopher K Gibu, Marilyn C Jones, Gladys A Ramos, Tara S Andreasen. Am J Med Genet A 2015
9
14


Idiopathic polyhydramnios and postnatal abnormalities.
Harald Abele, Sandra Starz, Markus Hoopmann, Britta Yazdi, Katharina Rall, Karl Oliver Kagan. Fetal Diagn Ther 2012
30
14

Perinatal outcomes of polyhydramnios without associated congenital fetal anomalies after the gestational age of 20 weeks.
Kuang-Chao Chen, Jui-Der Liou, Tai-Ho Hung, Dong-Ming Kuo, Jenn-Jeih Hsu, Ching-Chang Hsieh, Tsang-Tang Hsieh. Chang Gung Med J 2005
19
14

Performance of prenatal diagnosis in esophageal atresia.
Emmanuel Spaggiari, Giuliana Faure, Veronique Rousseau, Pascale Sonigo, Anne-Elodie Millischer-Bellaiche, Elsa Kermorvant-Duchemin, Francoise Muller, Isabelle Czerkiewicz, Yves Ville, Laurent J Salomon. Prenat Diagn 2015
26
14


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.