A citation-based method for searching scientific literature

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
Times Cited: 2







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
50

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
50


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
50

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
50

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
50

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
50


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
50

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
50

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
50


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
50

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
50


Fetal soft markers in obstetric ultrasound.
Michiel C Van den Hof, R Douglas Wilson. J Obstet Gynaecol Can 2005
69
50

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
50

Chromosomal microarray analysis for pregnancies with abnormal maternal serum screening who undergo invasive prenatal testing.
Xiaoqing Wu, Ying Li, Na Lin, Xiaorui Xie, Linjuan Su, Meiying Cai, Yuan Lin, Linshuo Wang, Meiying Wang, Liangpu Xu,[...]. J Cell Mol Med 2021
1
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
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
50

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
50

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
50

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
50

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
50

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
50

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
50

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
50



Parental age and risk of childhood cancers: a population-based cohort study from Sweden.
Benjamin H Yip, Yudi Pawitan, Kamila Czene. Int J Epidemiol 2006
101
50


Paternal age and schizophrenia: a population based cohort study.
Attila Sipos, Finn Rasmussen, Glynn Harrison, Per Tynelius, Glyn Lewis, David A Leon, David Gunnell. BMJ 2004
186
50

Parental and chromosomal origins of microdeletion and duplication syndromes involving 7q11.23, 15q11-q13 and 22q11.
N Simon Thomas, Miranda Durkie, Gemma Potts, Richard Sandford, Berendine Van Zyl, Sheila Youings, Nicholas R Dennis, Patricia A Jacobs. Eur J Hum Genet 2006
36
50

Increased paternal age and the influence on burden of genomic copy number variation in the general population.
Jacobine E Buizer-Voskamp, Hylke M Blauw, Marco P M Boks, Kristel R van Eijk, Jan H Veldink, Eric A M Hennekam, Jacob A S Vorstman, Flip Mulder, Henning Tiemeier, André G Uitterlinden,[...]. Hum Genet 2013
21
50

Incidence of sperm aneuploidy in relation to semen characteristics and assisted reproductive outcome.
L T Colombero, J J Hariprashad, M C Tsai, Z Rosenwaks, G D Palermo. Fertil Steril 1999
74
50

De novo copy number variants and parental age: Is there an association?
Isha Wadhawan, Yang Hai, Nastaran Foyouzi Yousefi, Xiuqing Guo, John M Graham, Jill A Rosenfeld. Eur J Med Genet 2020
1
100

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
50

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
50

Paternal age and the risk of birth defects in Norway.
Method Kazaura, Rolv T Lie, Rolv Skjaerven. Ann Epidemiol 2004
40
50

The effect of paternal age on fetal birth outcomes.
Amina P Alio, Hamisu M Salihu, Cheri McIntosh, Euna M August, Hanna Weldeselasse, Emanny Sanchez, Alfred K Mbah. Am J Mens Health 2012
56
50

De novo copy number variants associated with intellectual disability have a paternal origin and age bias.
Jayne Y Hehir-Kwa, Benjamín Rodríguez-Santiago, Lisenka E Vissers, Nicole de Leeuw, Rolph Pfundt, Jan K Buitelaar, Luis A Pérez-Jurado, Joris A Veltman. J Med Genet 2011
75
50

Paternal age as a risk factor for low birthweight.
Nancy E Reichman, Julien O Teitler. Am J Public Health 2006
64
50

An unexpected finding: younger fathers have a higher risk for offspring with chromosomal aneuploidies.
Bernhard Steiner, Rahim Masood, Kaspar Rufibach, Dunja Niedrist, Oliver Kundert, Mariluce Riegel, Albert Schinzel. Eur J Hum Genet 2015
18
50

The observed human sperm mutation frequency cannot explain the achondroplasia paternal age effect.
Irene Tiemann-Boege, William Navidi, Raji Grewal, Dan Cohn, Brenda Eskenazi, Andrew J Wyrobek, Norman Arnheim. Proc Natl Acad Sci U S A 2002
100
50

Prenatal diagnosis by chromosomal microarray analysis.
Brynn Levy, Ronald Wapner. Fertil Steril 2018
89
50

Paternal age and congenital malformations.
Jin Liang Zhu, Kreesten M Madsen, Mogens Vestergaard, Anne V Olesen, Olga Basso, Jørn Olsen. Hum Reprod 2005
71
50

Genomic microarray in fetuses with increased nuchal translucency and normal karyotype: a systematic review and meta-analysis.
M Grande, F A R Jansen, Y J Blumenfeld, A Fisher, A O Odibo, M C Haak, A Borrell. Ultrasound Obstet Gynecol 2015
80
50

Paternal Age Explains a Major Portion of De Novo Germline Mutation Rate Variability in Healthy Individuals.
Simon L Girard, Cynthia V Bourassa, Louis-Philippe Lemieux Perreault, Marc-André Legault, Amina Barhdadi, Amirthagowri Ambalavanan, Mara Brendgen, Frank Vitaro, Anne Noreau, Ginette Dionne,[...]. PLoS One 2016
20
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.