A citation-based method for searching scientific literature

Gorazd Rudolf, Luca Lovrečić, Nataša Tul, Nataša Teran, Borut Peterlin. Mol Genet Genomic Med 2019
Times Cited: 3







List of co-cited articles
4 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

Prenatal SNP array testing in 1000 fetuses with ultrasound anomalies: causative, unexpected and susceptibility CNVs.
Malgorzata I Srebniak, Karin Em Diderich, Marieke Joosten, Lutgarde Cp Govaerts, Jeroen Knijnenburg, Femke At de Vries, Marjan Boter, Debora Lont, Maarten Fcm Knapen, Merel C de Wit,[...]. Eur J Hum Genet 2016
38
66


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
66

Ultrasonographically detectable markers of fetal chromosomal abnormalities.
K H Nicolaides, R J Snijders, C M Gosden, C Berry, S Campbell. Lancet 1992
210
33

Interstitial duplication of 2q32.1-q33.3 in a patient with epilepsy, developmental delay, and autistic behavior.
Daisuke Usui, Shino Shimada, Keiko Shimojima, Midori Sugawara, Hajime Kawasaki, Hideo Shigematu, Yukitoshi Takahashi, Yushi Inoue, Katsumi Imai, Toshiyuki Yamamoto. Am J Med Genet A 2013
16
33


Clinical utility of array comparative genomic hybridisation in prenatal setting.
Luca Lovrecic, Ziga Iztok Remec, Marija Volk, Gorazd Rudolf, Karin Writzl, Borut Peterlin. BMC Med Genet 2016
9
33

A common cognitive, psychiatric, and dysmorphic phenotype in carriers of NRXN1 deletion.
Marina Viñas-Jornet, Susanna Esteba-Castillo, Elisabeth Gabau, Núria Ribas-Vidal, Neus Baena, Joan San, Anna Ruiz, Maria Dolors Coll, Ramon Novell, Miriam Guitart. Mol Genet Genomic Med 2014
23
33


Array-Comparative Genomic Hybridization Analysis in Fetuses with Major Congenital Malformations Reveals that 24% of Cases Have Pathogenic Deletions/Duplications.
Eleonora Di Gregorio, Giorgia Gai, Giovanni Botta, Alessandro Calcia, Patrizia Pappi, Flavia Talarico, Elisa Savin, Marisa Ribotta, Andrea Zonta, Cecilia Mancini,[...]. Cytogenet Genome Res 2015
2
50

Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype.
G D'Amours, Z Kibar, G Mathonnet, R Fetni, F Tihy, V Désilets, S Nizard, J L Michaud, E Lemyre. Clin Genet 2012
58
33

A unique case of a discontinuous duplication 3q26.1-3q28 resulting from a segregation error of a maternal complex chromosomal rearrangement involving an insertion and an inversion.
Laura Rodríguez, Samarth S Bhatt, Mónica García-Castro, Ana Plasencia, Joaquín Fernández-Toral, Elena Abarca, Marcelo de Bello Cioffi, Thomas Liehr. Gene 2014
7
33

Partial trisomy 2q: report of a patient with dup (2)(q33.1q35).
Courtney Drake Sebold, Susan Romie, Jadwiga Szymanska, Wilfredo Torres-Martinez, Virginia Thurston, Catherine Muesing, Gail H Vance. Am J Med Genet A 2005
9
33

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
33

Investigation of NRXN1 deletions: clinical and molecular characterization.
Mindy Preston Dabell, Jill A Rosenfeld, Patricia Bader, Luis F Escobar, Dima El-Khechen, Stephanie E Vallee, Mary Beth Palko Dinulos, Cynthia Curry, Jamie Fisher, Raymond Tervo,[...]. Am J Med Genet A 2013
69
33

New genetic testing in prenatal diagnosis.
Natalia Babkina, John M Graham. Semin Fetal Neonatal Med 2014
15
33

1.15 Mb microdeletion in chromosome band 20p13 associated with moderate developmental delay-additional case and data's review.
Aleksandra Jezela-Stanek, Marzena Kucharczyk, Magdalena Pelc, Anna Gutkowska, Małgorzata Krajewska-Walasek. Am J Med Genet A 2013
6
33

Duplication of 20qter and deletion of 20pter due to paternal pericentric inversion: patient report and review of 20qter duplications.
Lois J Starr, Edward J Truemper, Diane L Pickering, Warren G Sanger, Ann Haskins Olney. Am J Med Genet A 2014
1
100

Array comparative genomic hybridization in prenatal diagnosis: another experience.
F Vialard, D Molina Gomes, B Leroy, E Quarello, A Escalona, C Le Sciellour, V Serazin, J Roume, Y Ville, P de Mazancourt,[...]. Fetal Diagn Ther 2009
58
33

Molecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literature.
Frédérique Béna, Damien L Bruno, Mats Eriksson, Conny van Ravenswaaij-Arts, Zornitza Stark, Trijnie Dijkhuizen, Erica Gerkes, Stefania Gimelli, Devika Ganesamoorthy, Ann Charlotte Thuresson,[...]. Am J Med Genet B Neuropsychiatr Genet 2013
68
33

Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformations.
C Le Caignec, M Boceno, P Saugier-Veber, S Jacquemont, M Joubert, A David, T Frebourg, J M Rival. J Med Genet 2005
147
33

The prevalence of congenital anomalies in Europe.
Helen Dolk, Maria Loane, Ester Garne. Adv Exp Med Biol 2010
259
33

Application of Array Comparative Genomic Hybridization in Newborns with Multiple Congenital Anomalies.
Krzysztof Szczałuba, Beata Nowakowska, Katarzyna Sobecka, Marta Smyk, Jennifer Castaneda, Jakub Klapecki, Anna Kutkowska-Kaźmierczak, Robert Śmigiel, Ewa Bocian, Marek Radkowski,[...]. Adv Exp Med Biol 2016
3
33

The human clinical phenotypes of altered CHRNA7 copy number.
Madelyn A Gillentine, Christian P Schaaf. Biochem Pharmacol 2015
55
33

Should determination of the karyotype be systematic for all malformations detected by obstetrical ultrasound?
M Staebler, C Donner, N Van Regemorter, L Duprez, V De Maertelaer, F Devreker, F Avni. Prenat Diagn 2005
31
33

6p subtelomere deletion with congenital glaucoma, severe mental retardation, and growth impairment.
Takaya Nakane, Nakamura Kousuke, Hata Sonoko, Kamiya Yuko, Hidenori Sato, Takeo Kubota, Kanji Sugita. Pediatr Int 2013
12
33

A retrospective study by oligonucleotide array-CGH analysis in 50 fetuses with multiple malformations.
M Valduga, C Philippe, P Bach Segura, O Thiebaugeorges, A Miton, M Beri, C Bonnet, C Nemos, B Foliguet, P Jonveaux. Prenat Diagn 2010
54
33

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
33

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
33


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
33

Quality aspects of prenatal cytogenetic diagnosis: determining the effect of various factors involved in handling amniotic fluid and chorionic villus material for cytogenetic diagnosis.
Birgit Sikkema-Raddatz, Ron Suijkerbuijk, Katelijne Bouman, Bauke de Jong, Charles H C M Buys, Gerard J te Meerman. Prenat Diagn 2006
7
33


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
33

Whole Exome Sequencing: Applications in Prenatal Genetics.
Angie C Jelin, Neeta Vora. Obstet Gynecol Clin North Am 2018
23
33

Comprehensive genetic analysis of pregnancy loss by chromosomal microarrays: outcomes, benefits, and challenges.
Trilochan Sahoo, Natasa Dzidic, Michelle N Strecker, Sara Commander, Mary K Travis, Charles Doherty, R Weslie Tyson, Arturo E Mendoza, Mary Stephenson, Craig A Dise,[...]. Genet Med 2017
60
33

Chromosomal microarray analysis as a first-line test in pregnancies with a priori low risk for the detection of submicroscopic chromosomal abnormalities.
Francesco Fiorentino, Stefania Napoletano, Fiorina Caiazzo, Mariateresa Sessa, Sara Bono, Letizia Spizzichino, Anthony Gordon, Andrea Nuccitelli, Giuseppe Rizzo, Marina Baldi. Eur J Hum Genet 2013
61
33

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
33

Amniotic fluid culture failure: clinical significance and association with aneuploidy.
R Reid, W Sepulveda, P M Kyle, G Davies. Obstet Gynecol 1996
9
33

Prenatal diagnosis by chromosomal microarray analysis.
Brynn Levy, Ronald Wapner. Fertil Steril 2018
89
33

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
33

Chromosomal Microarray Analysis Results From Pregnancies With Various Ultrasonographic Anomalies.
Lena Sagi-Dain, Idit Maya, Adi Reches, Ayala Frumkin, Julia Grinshpun-Cohen, Reeval Segel, Esther Manor, Morad Khayat, Tamar Tenne, Ehud Banne,[...]. Obstet Gynecol 2018
14
33

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
33

Whole-exome sequencing on deceased fetuses with ultrasound anomalies: expanding our knowledge of genetic disease during fetal development.
Carin L Yates, Kristin G Monaghan, Deborah Copenheaver, Kyle Retterer, Julie Scuffins, Cathlin R Kucera, Bethany Friedman, Gabriele Richard, Jane Juusola. Genet Med 2017
59
33

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
33

Triploidy - variability of sonographic phenotypes.
Diana Massalska, Julia Bijok, Alicja Ilnicka, Grzegorz Jakiel, Tomasz Roszkowski. Prenat Diagn 2017
12
33

Tissue sampling technique affects accuracy of karyotype from missed abortions.
Ruth B Lathi, Amin A Milki. J Assist Reprod Genet 2002
44
33

Karyotype versus microarray testing for genetic abnormalities after stillbirth.
Uma M Reddy, Grier P Page, George R Saade, Robert M Silver, Vanessa R Thorsten, Corette B Parker, Halit Pinar, Marian Willinger, Barbara J Stoll, Josefine Heim-Hall,[...]. N Engl J Med 2012
140
33

Comparison of cytogenetics and molecular karyotyping for chromosome testing of miscarriage specimens.
Meera Sridhar Shah, Cengiz Cinnioglu, Melissa Maisenbacher, Ioanna Comstock, Jonathan Kort, Ruth Bunker Lathi. Fertil Steril 2017
24
33


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.