A citation-based method for searching scientific literature

E Zrnová, V Vranová, I Slámová, R Gaillyová, P Kuglík. Folia Biol (Praha) 2011
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Chromosome 8p23.2-pter: a critical region for mental retardation, autism and epilepsy?
A Nucaro, T Pisano, I Chillotti, C Montaldo, D Pruna. Clin Genet 2011
11
50


Ring chromosome 14 mosaicism: an unusual case associated with developmental delay and epilepsy, characterized by genome array-CGH.
Anna Lisa Nucaro, Melania Falchi, Tiziana Pisano, Rossano Rossino, Francesca Boscarelli, Giusi Stoico, Angela Milia, Caterina Montaldo, Carlo Cianchetti, Dario Pruna. Am J Med Genet A 2010
8
50

A novel giant gene CSMD3 encoding a protein with CUB and sushi multiple domains: a candidate gene for benign adult familial myoclonic epilepsy on human chromosome 8q23.3-q24.1.
Atsushi Shimizu, Shuichi Asakawa, Takashi Sasaki, Satoru Yamazaki, Hidehisa Yamagata, Jun Kudoh, Shinsei Minoshima, Ikuko Kondo, Nobuyoshi Shimizu. Biochem Biophys Res Commun 2003
54
50

Two patients with balanced translocations and autistic disorder: CSMD3 as a candidate gene for autism found in their common 8q23 breakpoint area.
Chiara Floris, Stefania Rassu, Loredana Boccone, Daniela Gasperini, Antonio Cao, Laura Crisponi. Eur J Hum Genet 2008
27
50

Molecular karyotyping: array CGH quality criteria for constitutional genetic diagnosis.
Joris R Vermeesch, Cindy Melotte, Guy Froyen, Steven Van Vooren, Binita Dutta, Nicole Maas, Stefan Vermeulen, Björn Menten, Frank Speleman, Bart De Moor,[...]. J Histochem Cytochem 2005
129
50

Array CGH in patients with learning disability (mental retardation) and congenital anomalies: updated systematic review and meta-analysis of 19 studies and 13,926 subjects.
Gurdeep S Sagoo, Adam S Butterworth, Simon Sanderson, Charles Shaw-Smith, Julian P T Higgins, Hilary Burton. Genet Med 2009
149
50


The human SLC8A3 gene and the tissue-specific Na+/Ca2+ exchanger 3 isoforms.
Nadia Gabellini, Stefania Bortoluzzi, Gian A Danieli, Ernesto Carafoli. Gene 2002
18
50

Characterization of Potocki-Lupski syndrome (dup(17)(p11.2p11.2)) and delineation of a dosage-sensitive critical interval that can convey an autism phenotype.
Lorraine Potocki, Weimin Bi, Diane Treadwell-Deering, Claudia M B Carvalho, Anna Eifert, Ellen M Friedman, Daniel Glaze, Kevin Krull, Jennifer A Lee, Richard Alan Lewis,[...]. Am J Hum Genet 2007
254
50



Monozygotic twins discordant for vaginal agenesis and bilateral tibial longitudinal deficiency.
Michael P Steinkampf, Sejal P Dharia, Ryan D Dickerson. Fertil Steril 2003
24
50


Müllerian agenesis: etiology, diagnosis, and management.
M Folch, I Pigem, J C Konje. Obstet Gynecol Surv 2000
78
50

Congenital absence of the vagina. The Mayer-Rokitansky-Kuster-Hauser syndrome.
J E Griffin, C Edwards, J D Madden, M J Harrod, J D Wilson. Ann Intern Med 1976
270
50


Right esophageal lung in a preterm child with VACTERL association and Mayer-Rokitansky-Kuster-Hauser syndrome.
F Linke, W Kraemer, M Ansorge, R Brzezinska, S Berger. Pediatr Surg Int 2005
13
50

A Robertsonian Translocation rob (14;15) (q10:q10) in a Patient with Recurrent Abortions: A Case Report.
Venkateshwari Ananthapur, Srilekha Avvari, Sunitha Tella, Pratibha Nallari, Jyothy Akka. J Reprod Infertil 2010
9
50

Report of a del22q11 in a patient with Mayer-Rokitansky-Küster-Hauser (MRKH) anomaly and exclusion of WNT-4, RAR-gamma, and RXR-alpha as major genes determining MRKH anomaly in a study of 25 affected women.
Carola Cheroki, Ana Cristina Krepischi-Santos, Carla Rosenberg, Fernanda Sarquis Jehee, Regina Célia Mingroni-Netto, Ivo Pavanello Filho, Sebastião Zanforlin Filho, Chong Ae Kim, Vicente R Bagnoli, Berenice B Mendonça,[...]. Am J Med Genet A 2006
48
50

A de novo sSMC(22) Characterized by High-Resolution Arrays in a Girl with Cat-Eye Syndrome without Coloboma.
C Córdova-Fletes, M G Domínguez, A Vázquez-Cárdenas, L E Figuera, V A Neira, A Rojas-Martínez, R Ortiz-López. Mol Syndromol 2012
3
50

Chromosomal segregation in spermatozoa of 14 Robertsonian translocation carriers.
Gonul Ogur, Elvire Van Assche, Walter Vegetti, Greta Verheyen, Herman Tournaye, Maryse Bonduelle, André Van Steirteghem, Inge Liebaers. Mol Hum Reprod 2006
57
50

Distinct effects of allelic NFIX mutations on nonsense-mediated mRNA decay engender either a Sotos-like or a Marshall-Smith syndrome.
Valérie Malan, Diana Rajan, Sophie Thomas, Adam C Shaw, Hélène Louis Dit Picard, Valérie Layet, Marianne Till, Arie van Haeringen, Geert Mortier, Sheela Nampoothiri,[...]. Am J Hum Genet 2010
89
50

Mayer-Rokitansky-Küester-Hauser (MRKH) syndrome with rectovestibular fistula and imperforate anus.
Shu Wang, Jing He Lang, Lan Zhu. Eur J Obstet Gynecol Reprod Biol 2010
9
50


WNT4 deficiency--a clinical phenotype distinct from the classic Mayer-Rokitansky-Kuster-Hauser syndrome: a case report.
A Biason-Lauber, G De Filippo, D Konrad, G Scarano, A Nazzaro, E J Schoenle. Hum Reprod 2007
115
50

Congenital genitourinary abnormalities in children with Williams-Beuren syndrome.
Zein M Sammour, Cristiano M Gomes, Jose de Bessa, Marcello S Pinheiro, Chong A E Kim, Marcelo Hisano, Homero Bruschini, Miguel Srougi. J Pediatr Urol 2014
17
50


Report of a girl with Klippel-feil syndrome and Poland anomaly.
M Erol, H Caksen, O Tan, B Atik, O Unal, D Odabaş. Genet Couns 2004
12
50

Higher incidence of linked malformations in siblings of Mayer-Rokitansky-Küster-Hauser-syndrome patients.
M Wottgen, S Brucker, S P Renner, P L Strissel, R Strick, A Kellermann, D Wallwiener, M W Beckmann, P Oppelt. Hum Reprod 2008
18
50

Role of TBX1 in human del22q11.2 syndrome.
Hisato Yagi, Yoshiyuki Furutani, Hiromichi Hamada, Takashi Sasaki, Shuichi Asakawa, Shinsei Minoshima, Fukiko Ichida, Kunitaka Joo, Misa Kimura, Shin-ichiro Imamura,[...]. Lancet 2003
526
50

Hereditary renal adysplasia, pulmonary hypoplasia and Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: a case report.
Pedro Acién, Francisco Galán, Irene Manchón, Eva Ruiz, Maribel Acién, Luis A Alcaraz. Orphanet J Rare Dis 2010
15
50


High incidence of recurrent copy number variants in patients with isolated and syndromic Müllerian aplasia.
Serena Nik-Zainal, Reiner Strick, Mekayla Storer, Ni Huang, Roland Rad, Lionel Willatt, Tomas Fitzgerald, Vicki Martin, Richard Sandford, Nigel P Carter,[...]. J Med Genet 2011
69
50

Clinical aspects of Mayer-Rokitansky-Kuester-Hauser syndrome: recommendations for clinical diagnosis and staging.
Peter Oppelt, Stefan P Renner, Anja Kellermann, Sara Brucker, Georges A Hauser, Kurt S Ludwig, Pamela L Strissel, Reiner Strick, Diethelm Wallwiener, Matthias W Beckmann. Hum Reprod 2006
168
50

A combination of transcriptome and methylation analyses reveals embryologically-relevant candidate genes in MRKH patients.
Katharina Rall, Gianmaria Barresi, Michael Walter, Sven Poths, Karina Haebig, Karin Schaeferhoff, Birgitt Schoenfisch, Olaf Riess, Diethelm Wallwiener, Michael Bonin,[...]. Orphanet J Rare Dis 2011
36
50

Recurrent aberrations identified by array-CGH in patients with Mayer-Rokitansky-Küster-Hauser syndrome.
Susanne Ledig, Cordula Schippert, Reiner Strick, Matthias W Beckmann, Patricia G Oppelt, Peter Wieacker. Fertil Steril 2011
86
50

Malformations in a cohort of 284 women with Mayer-Rokitansky-Küster-Hauser syndrome (MRKH).
Patricia G Oppelt, Johannes Lermann, Reiner Strick, Ralf Dittrich, Pamela Strissel, Ingo Rettig, Christine Schulze, Stefan P Renner, Matthias W Beckmann, Sara Brucker,[...]. Reprod Biol Endocrinol 2012
57
50

Mayer-Rokitansky-Kuster-Hauser syndrome with H-type anovestibular fistula.
Jai Kumar Mahajan, M A Venkatesh, Monika Bawa, Katargadda L N Rao. J Pediatr Surg 2009
9
50


MURCS and VACTERL association in a 27 year old female.
S L Balusamy, D Kumar, S R Subrahmanian. J Obstet Gynaecol 2009
3
50

Utero-vaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome) associated with deletions in known DiGeorge or DiGeorge-like loci.
Karine Morcel, Tanguy Watrin, Laurent Pasquier, Lucie Rochard, Cédric Le Caignec, Christèle Dubourg, Philippe Loget, Bernard-Jean Paniel, Sylvie Odent, Véronique David,[...]. Orphanet J Rare Dis 2011
34
50

Acquired inv(9): what is its significance?
Jaime L Betz, Ahmed S Behairy, Pedro Rabionet, Budi Tirtorahardjo, Mathew W Moore, Philip D Cotter. Cancer Genet Cytogenet 2005
18
50


Bilateral ovarian agenesis and the presence of the testis-specific protein 1-Y-linked gene: two new features of Mayer-Rokitansky-Küster-Hauser syndrome.
Eirini Plevraki, Marina Kita, Dimitrios G Goulis, Hariklia Hatzisevastou-Loukidou, Alexandros F Lambropoulos, Avraam Avramides. Fertil Steril 2004
21
50

Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome.
Karine Morcel, Laure Camborieux, Daniel Guerrier. Orphanet J Rare Dis 2007
199
50

Prevalence of Angelman syndrome and Prader-Willi syndrome in Estonian children: sister syndromes not equally represented.
Eve Oiglane-Shlik, Tiina Talvik, Riina Zordania, Haide Põder, Tiina Kahre, Elve Raukas, Tiiu Ilus, Gunnar Tasa, Oliver Bartsch, Marja-Leena Väisänen,[...]. Am J Med Genet A 2006
19
50

Acquired Robertsonian translocations in two leukemia patients.
D Chinnappan, A Philip, X Wu, A Pan, H E Wyandt. Cancer Genet Cytogenet 2001
6
50

VACTERL/VATER Association.
Benjamin D Solomon. Orphanet J Rare Dis 2011
194
50

Thrombocytopenia-absent radius syndrome.
Helga V Toriello. Semin Thromb Hemost 2011
37
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.