A citation-based method for searching scientific literature

Xiaoqing Wu, Ying Li, Na Lin, Xiaorui Xie, Linjuan Su, Meiying Cai, Yuan Lin, Linshuo Wang, Meiying Wang, Liangpu Xu, Hailong Huang. J Cell Mol Med 2021
Times Cited: 1







List of co-cited articles
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
100

Chromosomal microarray analysis for pregnancies with or without ultrasound abnormalities in women of advanced maternal age.
Xiaoqing Wu, Gang An, Xiaorui Xie, Linjuan Su, Meiying Cai, Xuemei Chen, Ying Li, Na Lin, Deqin He, Meiying Wang,[...]. J Clin Lab Anal 2020
6
100


Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2.
Pauline Chaste, Stephan J Sanders, Kommu N Mohan, Lambertus Klei, Youeun Song, Michael T Murtha, Vanessa Hus, Jennifer K Lowe, A Jeremy Willsey, Daniel Moreno-De-Luca,[...]. Autism Res 2014
44
100

High-resolution chromosomal microarrays in prenatal diagnosis significantly increase diagnostic power.
Beatrice Oneda, Rosa Baldinger, Regina Reissmann, Irina Reshetnikova, Pavel Krejci, Rahim Masood, Nicole Ochsenbein-Kölble, Deborah Bartholdi, Katharina Steindl, Denise Morotti,[...]. Prenat Diagn 2014
29
100

Chromosome microarray analysis should be offered to all invasive prenatal diagnostic testing following a normal rapid aneuploidy test result.
Laia Rodriguez-Revenga, Irene Madrigal, Antoni Borrell, Josep M Martinez, Joan Sabria, Lourdes Martin, Wladimiro Jimenez, Aurea Mira, Celia Badenas, Montserrat Milà. Clin Genet 2020
2
100

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
100

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
100


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
100

Uptake of noninvasive prenatal testing at a large academic referral center.
Sebastian Larion, Steven L Warsof, Letty Romary, Margaret Mlynarczyk, David Peleg, Alfred Z Abuhamad. Am J Obstet Gynecol 2014
61
100

Role of late amniocentesis in the era of modern genomic technologies.
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
7
100


15q11.2 microdeletion (BP1-BP2) and developmental delay, behaviour issues, epilepsy and congenital heart disease: a series of 52 patients.
Clémence Vanlerberghe, Florence Petit, Valérie Malan, Catherine Vincent-Delorme, Sonia Bouquillon, Odile Boute, Muriel Holder-Espinasse, Bruno Delobel, Bénédicte Duban, Louis Vallee,[...]. Eur J Med Genet 2015
49
100

First and second trimester antenatal screening for Down's syndrome: the results of the Serum, Urine and Ultrasound Screening Study (SURUSS).
N J Wald, C Rodeck, A K Hackshaw, J Walters, L Chitty, A M Mackinson. Health Technol Assess 2003
170
100


Fetal soft markers in obstetric ultrasound.
Michiel C Van den Hof, R Douglas Wilson. J Obstet Gynaecol Can 2005
69
100

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
100

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
100

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
100

X-linked ichthyosis: Molecular findings in four pedigrees with inconspicuous clinical manifestations.
Min Zhang, Hailong Huang, Na Lin, Shuqiong He, Gang An, Yan Wang, Meihuan Chen, Lingji Chen, Yuan Lin, Liangpu Xu. J Clin Lab Anal 2020
3
100

Estimates of penetrance for recurrent pathogenic copy-number variations.
Jill A Rosenfeld, Bradley P Coe, Evan E Eichler, Howard Cuckle, Lisa G Shaffer. Genet Med 2013
184
100

Pandora's pregnancy: NIPT, CMA, and genome sequencing-A new era for prenatal genetic testing.
Yael Hashiloni-Dolev, Tamar Nov-Klaiman, Aviad Raz. Prenat Diagn 2019
10
100

Benefits and burdens of using a SNP array in pregnancies at increased risk for the common aneuploidies.
Diane Van Opstal, Femke de Vries, Lutgarde Govaerts, Marjan Boter, Debora Lont, Stefanie van Veen, Marieke Joosten, Karin Diderich, Robert-Jan Galjaard, Malgorzata I Srebniak. Hum Mutat 2015
41
100

Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities.
Malgorzata I Srebniak, Marjan Boter, Gretel O Oudesluijs, Titia Cohen-Overbeek, Lutgarde Cp Govaerts, Karin Em Diderich, Renske Oegema, Maarten Fcm Knapen, Ingrid Mbh van de Laar, Marieke Joosten,[...]. Mol Cytogenet 2012
52
100

X-linked ichthyosis: Clinical and molecular findings in 35 Italian patients.
Andrea Diociaiuti, Adriano Angioni, Elisa Pisaneschi, Viola Alesi, Giovanna Zambruno, Antonio Novelli, May El Hachem. Exp Dermatol 2019
10
100

Should We Report 15q11.2 BP1-BP2 Deletions and Duplications in the Prenatal Setting?
Idit Maya, Sharon Perlman, Mordechai Shohat, Sarit Kahana, Shiri Yacobson, Tamar Tenne, Ifaat Agmon-Fishman, Reut Tomashov Matar, Lina Basel-Salmon, Rivka Sukenik-Halevy. J Clin Med 2020
1
100

Non-Invasive Prenatal Testing (NIPT) in pregnancies with trisomy 21, 18 and 13 performed in a public setting - factors of importance for correct interpretation of results.
Tanja S Hartwig, Louise Ambye, Lene Werge, Martin Kenneth Weiergang, Pernille Nørgaard, Steen Sørensen, Finn Stener Jørgensen. Eur J Obstet Gynecol Reprod Biol 2018
12
100




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.