A citation-based method for searching scientific literature

Yanling Dong, Shu Liu, Junnan Li, Jian Li, Qian Chen, Jianyun Luo, Chunlei Li, Huifan Li, Hongbo Qi, Rong Li. Mol Med Rep 2019
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.
K Buiting, S Saitoh, S Gross, B Dittrich, S Schwartz, R D Nicholls, B Horsthemke. Nat Genet 1995
465
50

Maternally inherited Birk Barel mental retardation dysmorphism syndrome caused by a mutation in the genomically imprinted potassium channel KCNK9.
Ortal Barel, Stavit A Shalev, Rivka Ofir, Asi Cohen, Joel Zlotogora, Zamir Shorer, Galia Mazor, Gal Finer, Shareef Khateeb, Noam Zilberberg,[...]. Am J Hum Genet 2008
103
25

Temple syndrome: improving the recognition of an underdiagnosed chromosome 14 imprinting disorder: an analysis of 51 published cases.
Yiannis Ioannides, Kemi Lokulo-Sodipe, Deborah J G Mackay, Justin H Davies, I Karen Temple. J Med Genet 2014
102
25

Novel fetal and maternal sonographic findings in confirmed cases of Beckwith-Wiedemann syndrome.
Karl Oliver Kagan, Christoph Berg, Andreas Dufke, Annegret Geipel, Markus Hoopmann, Harald Abele. Prenat Diagn 2015
22
25


Biallelic PADI6 variants linking infertility, miscarriages, and hydatidiform moles.
JianHua Qian, Ngoc Minh Phuong Nguyen, Maryam Rezaei, Bo Huang, YongLing Tao, XiaoFei Zhang, Qi Cheng, HanJin Yang, Ao Asangla, Jacek Majewski,[...]. Eur J Hum Genet 2018
30
25

Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci.
Salah Azzi, Sylvie Rossignol, Virginie Steunou, Theo Sas, Nathalie Thibaud, Fabienne Danton, Maryline Le Jule, Claudine Heinrichs, Sylvie Cabrol, Christine Gicquel,[...]. Hum Mol Genet 2009
153
25

Molecular and clinical studies in 8 patients with Temple syndrome.
G Gillessen-Kaesbach, B Albrecht, T Eggermann, M Elbracht, D Mitter, S Morlot, C M A van Ravenswaaij-Arts, S Schulz, G Strobl-Wildemann, K Buiting,[...]. Clin Genet 2018
11
25

Genomic imprinting disorders: lessons on how genome, epigenome and environment interact.
David Monk, Deborah J G Mackay, Thomas Eggermann, Eamonn R Maher, Andrea Riccio. Nat Rev Genet 2019
88
25

Cannabinoid exposure and altered DNA methylation in rat and human sperm.
Susan K Murphy, Nilda Itchon-Ramos, Zachary Visco, Zhiqing Huang, Carole Grenier, Rose Schrott, Kelly Acharya, Marie-Helene Boudreau, Thomas M Price, Douglas J Raburn,[...]. Epigenetics 2018
63
25

Diagnosis and management of Silver-Russell syndrome: first international consensus statement.
Emma L Wakeling, Frédéric Brioude, Oluwakemi Lokulo-Sodipe, Susan M O'Connell, Jennifer Salem, Jet Bliek, Ana P M Canton, Krystyna H Chrzanowska, Justin H Davies, Renuka P Dias,[...]. Nat Rev Endocrinol 2017
174
25

Trim28 is required for epigenetic stability during mouse oocyte to embryo transition.
Daniel M Messerschmidt, Wilhelmine de Vries, Mitsuteru Ito, Davor Solter, Anne Ferguson-Smith, Barbara B Knowles. Science 2012
211
25

The subcortical maternal complex: multiple functions for one biological structure?
D Bebbere, L Masala, D F Albertini, S Ledda. J Assist Reprod Genet 2016
31
25

Syndromic Disorders Caused by Disturbed Human Imprinting
Diana Carli, Evelise Riberi, Giovanni Battista Ferrero, Alessandro Mussa. J Clin Res Pediatr Endocrinol 2020
4
25

Clinical characterisation of the multiple maternal hypomethylation syndrome in siblings.
Susanne E Boonen, Sven Pörksen, Deborah Jg Mackay, Elsebet Oestergaard, Birthe Olsen, Karen Brondum-Nielsen, I Karen Temple, Johanne Md Hahnemann. Eur J Hum Genet 2008
36
25



Complex tissue-specific epigenotypes in Russell-Silver Syndrome associated with 11p15 ICR1 hypomethylation.
Salah Azzi, Annick Blaise, Virginie Steunou, Madeleine D Harbison, Jennifer Salem, Frédéric Brioude, Sylvie Rossignol, Walid Abi Habib, Nathalie Thibaud, Cristina Das Neves,[...]. Hum Mutat 2014
28
25

Update of the EMQN/ACGS best practice guidelines for molecular analysis of Prader-Willi and Angelman syndromes.
Jasmin Beygo, Karin Buiting, Simon C Ramsden, Rachael Ellis, Jill Clayton-Smith, Deniz Kanber. Eur J Hum Genet 2019
11
25

Developmental expression and subcellular localization of mouse MATER, an oocyte-specific protein essential for early development.
Zhi-Bin Tong, Lyn Gold, Anto De Pol, Konstantina Vanevski, Heidi Dorward, Paola Sena, Carla Palumbo, Carolyn A Bondy, Lawrence M Nelson. Endocrinology 2004
67
25

In embryonic stem cells, ZFP57/KAP1 recognize a methylated hexanucleotide to affect chromatin and DNA methylation of imprinting control regions.
Simon Quenneville, Gaetano Verde, Andrea Corsinotti, Adamandia Kapopoulou, Johan Jakobsson, Sandra Offner, Ilaria Baglivo, Paolo V Pedone, Giovanna Grimaldi, Andrea Riccio,[...]. Mol Cell 2011
345
25

The hydatidiform mole.
Jean-Jacques Candelier. Cell Adh Migr 2016
24
25

A novel IGF2/H19 domain triplication in the 11p15.5 imprinting region causing either Beckwith-Wiedemann or Silver-Russell syndrome in a single family.
Dorota Jurkiewicz, Monika Kugaudo, Agata Skórka, Robert Śmigiel, Marta Smyk, Elżbieta Ciara, Krystyna Chrzanowska, Małgorzata Krajewska-Walasek. Am J Med Genet A 2017
5
25

The human knockout phenotype of PADI6 is female sterility caused by cleavage failure of their fertilized eggs.
S Maddirevula, S Coskun, K Awartani, H Alsaif, F M Abdulwahab, F S Alkuraya. Clin Genet 2017
15
25

Mater, a maternal effect gene required for early embryonic development in mice.
Z B Tong, L Gold, K E Pfeifer, H Dorward, E Lee, C A Bondy, J Dean, L M Nelson. Nat Genet 2000
365
25

Cdkn1c Boosts the Development of Brown Adipose Tissue in a Murine Model of Silver Russell Syndrome.
Matthew Van De Pette, Simon J Tunster, Grainne I McNamara, Tatyana Shelkovnikova, Steven Millership, Lindsay Benson, Stuart Peirson, Mark Christian, Antonio Vidal-Puig, Rosalind M John. PLoS Genet 2016
17
25

Discrepant molecular and clinical diagnoses in Beckwith-Wiedemann and Silver-Russell syndromes.
Deborah J G Mackay, Jet Bliek, Maria Paola Lombardi, Silvia Russo, Luciano Calzari, Sara Guzzetti, Claudia Izzi, Angelo Selicorni, Daniela Melis, Karen Temple,[...]. Genet Res (Camb) 2019
6
25

A maternal hypomethylation syndrome presenting as transient neonatal diabetes mellitus.
D J G Mackay, S E Boonen, J Clayton-Smith, J Goodship, J M D Hahnemann, S G Kant, P R Njølstad, N H Robin, D O Robinson, R Siebert,[...]. Hum Genet 2006
108
25

6q24 transient neonatal diabetes.
I Karen Temple, Julian P H Shield. Rev Endocr Metab Disord 2010
45
25

NLRP5 mediates mitochondrial function in mouse oocytes and embryos.
Roxanne Fernandes, Chiharu Tsuda, Alagammal L Perumalsamy, Taline Naranian, Jasmine Chong, Beth M Acton, Zhi-Bin Tong, Lawrence M Nelson, Andrea Jurisicova. Biol Reprod 2012
40
25

Detection of fetal epigenetic biomarkers through genome-wide DNA methylation study for non-invasive prenatal diagnosis.
Hong-Dan Wang, Lin Liu, Hui-Ru Zhao, Qiao-Fang Hou, Jing-Bin Yan, Wei-Li Shi, Qian-Nan Guo, Li Wang, Shi-Xiu Liao, Bo-Feng Zhu. Mol Med Rep 2017
8
25

Regulatory links between imprinted genes: evolutionary predictions and consequences.
Manus M Patten, Michael Cowley, Rebecca J Oakey, Robert Feil. Proc Biol Sci 2016
25
25

Genomic imprinting in the human placenta.
David Monk. Am J Obstet Gynecol 2015
57
25

Paternally Inherited IGF2 Mutation and Growth Restriction.
Matthias Begemann, Birgit Zirn, Gijs Santen, Elisa Wirthgen, Lukas Soellner, Hans-Martin Büttel, Roland Schweizer, Wilbert van Workum, Gerhard Binder, Thomas Eggermann. N Engl J Med 2015
119
25

Expert consensus document: Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: an international consensus statement.
Frédéric Brioude, Jennifer M Kalish, Alessandro Mussa, Alison C Foster, Jet Bliek, Giovanni Battista Ferrero, Susanne E Boonen, Trevor Cole, Robert Baker, Monica Bertoletti,[...]. Nat Rev Endocrinol 2018
156
25

TLE6 mutation causes the earliest known human embryonic lethality.
Anas M Alazami, Salma M Awad, Serdar Coskun, Saad Al-Hassan, Hadia Hijazi, Firdous M Abdulwahab, Coralie Poizat, Fowzan S Alkuraya. Genome Biol 2015
81
25

Maternally expressed NLRP2 links the subcortical maternal complex (SCMC) to fertility, embryogenesis and epigenetic reprogramming.
Sangeetha Mahadevan, Varsha Sathappan, Budi Utama, Isabel Lorenzo, Khalied Kaskar, Ignatia B Van den Veyver. Sci Rep 2017
35
25

Segmental maternal uniparental disomy 7q associated with DLK1/GTL2 (14q32) hypomethylation.
Matthias Begemann, Sabrina Spengler, Ulrike Kordass, Carmen Schröder, Thomas Eggermann. Am J Med Genet A 2012
18
25

Differences in expression rather than methylation at placenta-specific imprinted loci is associated with intrauterine growth restriction.
Ana Monteagudo-Sánchez, Marta Sánchez-Delgado, Jose Ramon Hernandez Mora, Nuria Tubío Santamaría, Eduard Gratacós, Manel Esteller, Miguel López de Heredia, Virgina Nunes, Cecile Choux, Patricia Fauque,[...]. Clin Epigenetics 2019
9
25

Phenotypic spectrum and extent of DNA methylation defects associated with multilocus imprinting disturbances.
Susanne Bens, Julia Kolarova, Jasmin Beygo, Karin Buiting, Almuth Caliebe, Thomas Eggermann, Gabriele Gillessen-Kaesbach, Dirk Prawitt, Susanne Thiele-Schmitz, Matthias Begemann,[...]. Epigenomics 2016
12
25

Epigenetic regulation in development: is the mouse a good model for the human?
Courtney W Hanna, Hannah Demond, Gavin Kelsey. Hum Reprod Update 2018
33
25

Search for cis-acting factors and maternal effect variants in Silver-Russell patients with ICR1 hypomethylation and their mothers.
Lukas Soellner, Florian Kraft, Sabrina Sauer, Matthias Begemann, Ingo Kurth, Miriam Elbracht, Thomas Eggermann. Eur J Hum Genet 2019
7
25

Placenta-specific epimutation at H19-DMR among common pregnancy complications: its frequency and effect on the expression patterns of H19 and IGF2.
Yuko Yamaguchi, Chiharu Tayama, Junko Tomikawa, Rina Akaishi, Hiromi Kamura, Kentaro Matsuoka, Norio Wake, Hisanori Minakami, Kiyoko Kato, Takahiro Yamada,[...]. Clin Epigenetics 2019
5
25

Transgenerational Effects of Bisphenol A on Gene Expression and DNA Methylation of Imprinted Genes in Brain.
Zuzana Drobná, Anne D Henriksen, Jennifer T Wolstenholme, Catalina Montiel, Philip S Lambeth, Stephen Shang, Erin P Harris, Changqing Zhou, Jodi A Flaws, Mazhar Adli,[...]. Endocrinology 2018
42
25

Recurrent complete hydatidiform mole: where we are, is there a safe gestational horizon? Opinion and mini-review.
Ioannis Kalogiannidis, Kallirhoe Kalinderi, Michail Kalinderis, Dimosthenis Miliaras, Basil Tarlatzis, Apostolos Athanasiadis. J Assist Reprod Genet 2018
10
25

The genetics of recurrent hydatidiform moles in China: correlations between NLRP7 mutations, molar genotypes and reproductive outcomes.
Jianhua Qian, Qi Cheng, Sharlene Murdoch, Chengming Xu, Fan Jin, Wafaa Chebaro, Xiaofei Zhang, Huijuan Gao, Yimin Zhu, Rima Slim,[...]. Mol Hum Reprod 2011
32
25


Is ZFP57 binding to H19/IGF2:IG-DMR affected in Silver-Russell syndrome?
Angela Sparago, Flavia Cerrato, Andrea Riccio. Clin Epigenetics 2018
17
25

A mouse model of Angelman syndrome imprinting defects.
Michael W Lewis, Dorianmarie Vargas-Franco, Deborah A Morse, James L Resnick. Hum Mol Genet 2019
10
25



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.