A citation-based method for searching scientific literature

Marios Lange, Rodiola Begolli, Antonis Giakountis. Noncoding RNA 2021
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Chromosomal rearrangements in Xq and premature ovarian failure: mapping of 25 new cases and review of the literature.
Flavio Rizzolio, Silvia Bione, Cinzia Sala, Mara Goegan, Mattia Gentile, Giuliana Gregato, Elena Rossi, Tiziano Pramparo, Orsetta Zuffardi, Daniela Toniolo. Hum Reprod 2006
76
50

Exome Sequencing of a Primary Ovarian Insufficiency Cohort Reveals Common Molecular Etiologies for a Spectrum of Disease.
Angad Jolly, Yavuz Bayram, Serap Turan, Zehra Aycan, Tulay Tos, Zehra Yavas Abali, Bulent Hacihamdioglu, Zeynep Hande Coban Akdemir, Hadia Hijazi, Serpil Bas,[...]. J Clin Endocrinol Metab 2019
30
50

Targeting the Non-Coding Genome for the Diagnosis of Disorders of Sex Development.
Gabby Atlas, Rajini Sreenivasan, Andrew Sinclair. Sex Dev 2021
3
50

Genetics of premature ovarian insufficiency and the association with X-autosome translocations.
Adriana Di-Battista, Mariana Moysés-Oliveira, Maria Isabel Melaragno. Reproduction 2020
4
50

Identification of variants in pleiotropic genes causing "isolated" premature ovarian insufficiency: implications for medical practice.
Elena J Tucker, Sonia R Grover, Gorjana Robevska, Jocelyn van den Bergen, Chloe Hanna, Andrew H Sinclair. Eur J Hum Genet 2018
21
50

Whole-exome sequencing in patients with premature ovarian insufficiency: early detection and early intervention.
Hongli Liu, Xiaoli Wei, Yanwei Sha, Wensheng Liu, Haijie Gao, Jin Lin, Youzhu Li, Yaling Tang, Yifeng Wang, Yanlong Wang,[...]. J Ovarian Res 2020
15
50

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome.
A J Verkerk, M Pieretti, J S Sutcliffe, Y H Fu, D P Kuhl, A Pizzuti, O Reiner, S Richards, M F Victoria, F P Zhang. Cell 1991
50

Autoimmune primary ovarian insufficiency.
C A Silva, L Y S Yamakami, N E Aikawa, D B Araujo, J F Carvalho, E Bonfá. Autoimmun Rev 2014
86
50

Mutations in NR5A1 associated with ovarian insufficiency.
Diana Lourenço, Raja Brauner, Lin Lin, Arantzazu De Perdigo, Georges Weryha, Mihaela Muresan, Radia Boudjenah, Gil Guerra-Junior, Andréa T Maciel-Guerra, John C Achermann,[...]. N Engl J Med 2009
250
50

Cytogenetics of premature ovarian failure: an investigation on 269 affected women.
Simona Baronchelli, Donatella Conconi, Elena Panzeri, Angela Bentivegna, Serena Redaelli, Sara Lissoni, Fabiana Saccheri, Nicoletta Villa, Francesca Crosti, Elena Sala,[...]. J Biomed Biotechnol 2011
33
50


Alteration of protein function by a silent polymorphism linked to tRNA abundance.
Sebastian Kirchner, Zhiwei Cai, Robert Rauscher, Nicolai Kastelic, Melanie Anding, Andreas Czech, Bertrand Kleizen, Lynda S Ostedgaard, Ineke Braakman, David N Sheppard,[...]. PLoS Biol 2017
69
50

Study of the Genetic Etiology of Primary Ovarian Insufficiency: FMR1 Gene.
Maitane Barasoain, Gorka Barrenetxea, Iratxe Huerta, Mercedes Télez, Begoña Criado, Isabel Arrieta. Genes (Basel) 2016
18
50

Deregulation of key signaling pathways involved in oocyte maturation in FMR1 premutation carriers with Fragile X-associated primary ovarian insufficiency.
M I Alvarez-Mora, L Rodriguez-Revenga, I Madrigal, F Garcia-Garcia, M Duran, J Dopazo, X Estivill, M Milà. Gene 2015
9
50

Disruption of POF1B binding to nonmuscle actin filaments is associated with premature ovarian failure.
Arnaud Lacombe, Hane Lee, Laila Zahed, Mahmoud Choucair, Jean-Marc Muller, Stanley F Nelson, Wael Salameh, Eric Vilain. Am J Hum Genet 2006
75
50


Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndrome.
M V Bell, M C Hirst, Y Nakahori, R N MacKinnon, A Roche, T J Flint, P A Jacobs, N Tommerup, L Tranebjaerg, U Froster-Iskenius. Cell 1991
324
50

Mutant cohesin in premature ovarian failure.
Sandrine Caburet, Valerie A Arboleda, Elena Llano, Paul A Overbeek, Jose Luis Barbero, Kazuhiro Oka, Wilbur Harrison, Daniel Vaiman, Ziva Ben-Neriah, Ignacio García-Tuñón,[...]. N Engl J Med 2014
189
50

Genetics of human female infertility†.
Svetlana A Yatsenko, Aleksandar Rajkovic. Biol Reprod 2019
53
50

Genetics of primary ovarian insufficiency.
R Rossetti, I Ferrari, M Bonomi, L Persani. Clin Genet 2017
110
50

Characterization of a novel mutation V136L in bone morphogenetic protein 15 identified in a woman affected by POI.
Eleonora Ferrarini, Giuseppina De Marco, Francesca Orsolini, Elena Gianetti, Elena Benelli, Franca Fruzzetti, Tommaso Simoncini, Patrizia Agretti, Massimo Tonacchera. J Ovarian Res 2021
5
50

Hearing silence: non-neutral evolution at synonymous sites in mammals.
J V Chamary, Joanna L Parmley, Laurence D Hurst. Nat Rev Genet 2006
571
50

Porcine IGF1 synonymous mutation alter gene expression and protein binding affinity with IGF1R.
Yunyun Cheng, Songcai Liu, Gang Wang, Wenzhen Wei, Shan Huang, Rui Yang, Hongwei Geng, Haoyang Li, Jie Song, Lidan Sun,[...]. Int J Biol Macromol 2018
11
50

The p.G146A and p.P125P polymorphisms in the steroidogenic factor-1 (SF-1) gene do not affect the risk for hypospadias in Caucasians.
T Adamovic, Y Chen, H T T Thai, X Zhang, E Markljung, S Zhao, A Nordenskjöld. Sex Dev 2012
11
50

Investigating the role of X chromosome breakpoints in premature ovarian failure.
Simona Baronchelli, Nicoletta Villa, Serena Redaelli, Sara Lissoni, Fabiana Saccheri, Elena Panzeri, Donatella Conconi, Angela Bentivegna, Francesca Crosti, Elena Sala,[...]. Mol Cytogenet 2012
24
50

Varied phenotypic spectrum presenting of paroxysmal exercise-induced dyskinesia: a Turkish family with SLC2A1 mutation.
Murat Gultekin, Muhammet Ensar Dogan, Gulsah Simsir, Ayse Nazlı Basak. Neurol Sci 2021
1
100

A synonymous coding variant that alters ALAS2 splicing and causes X-linked sideroblastic anemia.
Jamie Heather Oakley, Dean R Campagna, Liang Sun, Shira Rockowitz, Piotr Sliz, Jeanne Boudreaux, Gary Woods, Mark D Fleming. Pediatr Blood Cancer 2022
1
100

Genetic determination of the ovarian reserve: a literature review.
Aleksandra V Moiseeva, Varvara A Kudryavtseva, Vladimir N Nikolenko, Marine M Gevorgyan, Ara L Unanyan, Anastassia A Bakhmet, Mikhail Y Sinelnikov. J Ovarian Res 2021
2
50


Genetic insights into biological mechanisms governing human ovarian ageing.
Katherine S Ruth, Felix R Day, Jazib Hussain, Ana Martínez-Marchal, Catherine E Aiken, Ajuna Azad, Deborah J Thompson, Lucie Knoblochova, Hironori Abe, Jane L Tarry-Adkins,[...]. Nature 2021
49
50


Epigenetic analysis of the critical region I for premature ovarian failure: demonstration of a highly heterochromatic domain on the long arm of the mammalian X chromosome.
F Rizzolio, T Pramparo, C Sala, O Zuffardi, L De Santis, E Rabellotti, F Calzi, F Fusi, R Bellazzi, D Toniolo. J Med Genet 2009
21
50

Molecular Characterization of FMR1 Gene by TP-PCR in Women of Reproductive Age and Women with Premature Ovarian Insufficiency.
Deepika Delsa Dean, Sarita Agarwal, Deepa Kapoor, Kuldeep Singh, Chandra Vati. Mol Diagn Ther 2018
5
50

Unique dominant negative mutation in the N-terminal mitochondrial targeting sequence of StAR, causing a variant form of congenital lipoid adrenal hyperplasia.
María Sonia Baquedano, Gabriela Guercio, Roxana Marino, Esperanza Berensztein, Mariana Costanzo, Marcela Bailez, Elisa Vaiani, Mercedes Maceiras, Pablo Ramirez, Eduardo Chaler,[...]. J Clin Endocrinol Metab 2013
11
50

Mutations in LARS2, encoding mitochondrial leucyl-tRNA synthetase, lead to premature ovarian failure and hearing loss in Perrault syndrome.
Sarah B Pierce, Ksenija Gersak, Rachel Michaelson-Cohen, Tom Walsh, Ming K Lee, Daniel Malach, Rachel E Klevit, Mary-Claire King, Ephrat Levy-Lahad. Am J Hum Genet 2013
142
50

Evaluation of the autoimmune regulator (AIRE) gene mutations in a cohort of Italian patients with autoimmune-polyendocrinopathy-candidiasis-ectodermal-dystrophy (APECED) and in their relatives.
Sara Cervato, Barbara Mariniello, Francesca Lazzarotto, Luca Morlin, Renato Zanchetta, Giorgio Radetti, Filippo De Luca, Mariella Valenzise, Roberta Giordano, Daniela Rizzo,[...]. Clin Endocrinol (Oxf) 2009
59
50

Molecular Genetics of Premature Ovarian Insufficiency.
Xue Jiao, Hanni Ke, Yingying Qin, Zi-Jiang Chen. Trends Endocrinol Metab 2018
95
50

Primary Ovarian Insufficiency.
Joop S E Laven. Semin Reprod Med 2016
40
50

New NOBOX mutations identified in a large cohort of women with primary ovarian insufficiency decrease KIT-L expression.
Justine Bouilly, Florence Roucher-Boulez, Anne Gompel, Hélène Bry-Gauillard, Kemal Azibi, Cherif Beldjord, Catherine Dodé, Jérôme Bouligand, Anne Guiochon Mantel, Annie-Claude Hécart,[...]. J Clin Endocrinol Metab 2015
34
50

Chromosomal abnormalities & oxidative stress in women with premature ovarian failure (POF).
Manoj Kumar, Dhananjay Pathak, Sundararajan Venkatesh, Alka Kriplani, A C Ammini, Rima Dada. Indian J Med Res 2012
22
50

Novel FOXL2 mutations cause blepharophimosis-ptosis-epicanthus inversus syndrome with premature ovarian insufficiency.
Xiao-Wen Yang, Wen-Bin He, Fei Gong, Wen Li, Xiu-Rong Li, Chang-Gao Zhong, Guang-Xiu Lu, Ge Lin, Juan Du, Yue-Qiu Tan. Mol Genet Genomic Med 2018
11
50

Molecular genetic and cytogenetic characterization of a partial Xp duplication and Xq deletion in a patient with premature ovarian failure.
Mi Kyoung Kim, Hyun Ha Seok, You Shin Kim, Mi Uk Chin, Se Ra Sung, Woo Sik Lee, Sung Han Shim, Tae Ki Yoon. Gene 2014
12
50

Genetics of primary ovarian insufficiency: new developments and opportunities.
Yingying Qin, Xue Jiao, Joe Leigh Simpson, Zi-Jiang Chen. Hum Reprod Update 2015
245
50

Exposing synonymous mutations.
Ryan C Hunt, Vijaya L Simhadri, Matthew Iandoli, Zuben E Sauna, Chava Kimchi-Sarfaty. Trends Genet 2014
195
50

Isolation of sequences that span the fragile X and identification of a fragile X-related CpG island.
D Heitz, F Rousseau, D Devys, S Saccone, H Abderrahim, D Le Paslier, D Cohen, A Vincent, D Toniolo, G Della Valle. Science 1991
174
50

BoxPlotR: a web tool for generation of box plots.
Michaela Spitzer, Jan Wildenhain, Juri Rappsilber, Mike Tyers. Nat Methods 2014
397
50

miR-15/107 microRNA Gene Group: Characteristics and Functional Implications in Cancer.
Chiara Turco, Sara Donzelli, Giulia Fontemaggi. Front Cell Dev Biol 2020
15
50

Identification of miR-508-3p and miR-509-3p that are associated with cell invasion and migration and involved in the apoptosis of renal cell carcinoma.
Qingna Zhai, Liang Zhou, Chunjuan Zhao, Jun Wan, Zhendong Yu, Xin Guo, Jie Qin, Jing Chen, Ruijing Lu. Biochem Biophys Res Commun 2012
84
50


P53-induced microRNA-107 inhibits HIF-1 and tumor angiogenesis.
Munekazu Yamakuchi, Craig D Lotterman, Clare Bao, Ralph H Hruban, Baktiar Karim, Joshua T Mendell, David Huso, Charles J Lowenstein. Proc Natl Acad Sci U S A 2010
306
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.