A citation-based method for searching scientific literature

Samuel W Baker, Kelly A Duffy, Jennifer Richards-Yutz, Matthew A Deardorff, Jennifer M Kalish, Arupa Ganguly. J Med Genet 2021
Times Cited: 5







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



Times Cited
  Times     Co-cited
Similarity


Characterization of the Beckwith-Wiedemann spectrum: Diagnosis and management.
Kelly A Duffy, Christopher M Cielo, Jennifer L Cohen, Christina X Gonzalez-Gandolfi, Jessica R Griff, Evan R Hathaway, Jonida Kupa, Jesse A Taylor, Kathleen H Wang, Arupa Ganguly,[...]. Am J Med Genet C Semin Med Genet 2019
21
80

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
60

Epigenetics and imprinting in human disease.
Jennifer M Kalish, Connie Jiang, Marisa S Bartolomei. Int J Dev Biol 2014
50
40

Human-ovine comparative sequencing of a 250-kb imprinted domain encompassing the callipyge (clpg) locus and identification of six imprinted transcripts: DLK1, DAT, GTL2, PEG11, antiPEG11, and MEG8.
C Charlier, K Segers, D Wagenaar, L Karim, S Berghmans, O Jaillon, T Shay, J Weissenbach, N Cockett, G Gyapay,[...]. Genome Res 2001
141
20

Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders.
Erfan Aref-Eshghi, Jennifer Kerkhof, Victor P Pedro, Mouna Barat-Houari, Nathalie Ruiz-Pallares, Jean-Christophe Andrau, Didier Lacombe, Julien Van-Gils, Patricia Fergelot, Christèle Dubourg,[...]. Am J Hum Genet 2020
29
20

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
20

Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes.
R D Nicholls, J L Knepper. Annu Rev Genomics Hum Genet 2001
410
20

Genomic imprinting in mammals.
Denise P Barlow, Marisa S Bartolomei. Cold Spring Harb Perspect Biol 2014
318
20

A large imprinted microRNA gene cluster at the mouse Dlk1-Gtl2 domain.
Hervé Seitz, Hélène Royo, Marie-Line Bortolin, Shau-Ping Lin, Anne C Ferguson-Smith, Jérôme Cavaillé. Genome Res 2004
388
20

Pref-1 interacts with fibronectin to inhibit adipocyte differentiation.
Yuhui Wang, Ling Zhao, Cynthia Smas, Hei Sook Sul. Mol Cell Biol 2010
94
20

Differential regulation of imprinting in the murine embryo and placenta by the Dlk1-Dio3 imprinting control region.
Shau-Ping Lin, Phil Coan, Simao Teixeira da Rocha, Herve Seitz, Jerome Cavaille, Pi-Wen Teng, Shuji Takada, Anne C Ferguson-Smith. Development 2007
82
20

The Dlk1 and Gtl2 genes are linked and reciprocally imprinted.
J V Schmidt, P G Matteson, B K Jones, X J Guan, S M Tilghman. Genes Dev 2000
255
20


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
20

Recommendations for the investigation of animal models of Prader-Willi syndrome.
James L Resnick, Robert D Nicholls, Rachel Wevrick. Mamm Genome 2013
28
20


Delta-like and gtl2 are reciprocally expressed, differentially methylated linked imprinted genes on mouse chromosome 12.
S Takada, M Tevendale, J Baker, P Georgiades, E Campbell, T Freeman, M H Johnson, M Paulsen, A C Ferguson-Smith. Curr Biol 2000
174
20

Parental origin-specific developmental defects in mice with uniparental disomy for chromosome 12.
P Georgiades, M Watkins, M A Surani, A C Ferguson-Smith. Development 2000
143
20

Establishment of paternal allele-specific DNA methylation at the imprinted mouse Gtl2 locus.
Kamila Nowak, Geneva Stein, Elizabeth Powell, Lu Mei He, Snehal Naik, Jane Morris, Sara Marlow, Tamara L Davis. Epigenetics 2011
21
20

Comprehensive clinical studies in 34 patients with molecularly defined UPD(14)pat and related conditions (Kagami-Ogata syndrome).
Masayo Kagami, Kenji Kurosawa, Osamu Miyazaki, Fumitoshi Ishino, Kentaro Matsuoka, Tsutomu Ogata. Eur J Hum Genet 2015
46
20

Overexpression of microRNAs from the Gtl2-Rian locus contributes to postnatal death in mice.
Soichiro Kumamoto, Nozomi Takahashi, Kayo Nomura, Makoto Fujiwara, Megumi Kijioka, Yoshinobu Uno, Yoichi Matsuda, Yusuke Sotomaru, Tomohiro Kono. Hum Mol Genet 2017
6
20

Epimutation (hypomethylation) affecting the chromosome 14q32.2 imprinted region in a girl with upd(14)mat-like phenotype.
Kana Hosoki, Tsutomu Ogata, Masayo Kagami, Touju Tanaka, Shinji Saitoh. Eur J Hum Genet 2008
30
20


Asymmetric regulation of imprinting on the maternal and paternal chromosomes at the Dlk1-Gtl2 imprinted cluster on mouse chromosome 12.
Shau-Ping Lin, Neil Youngson, Shuji Takada, Hervé Seitz, Wolf Reik, Martina Paulsen, Jerome Cavaille, Anne C Ferguson-Smith. Nat Genet 2003
363
20

Skeletal defects in paternal uniparental disomy for chromosome 14 are re-capitulated in the mouse model (paternal uniparental disomy 12).
V Reid Sutton, William H McAlister, Terry K Bertin, Sara Kaffe, Jin-Chen C Wang, Shoji Yano, Lisa G Shaffer, Brendan Lee, Charles J Epstein, Angela J Villar. Hum Genet 2003
25
20

Gtl2lacZ, an insertional mutation on mouse chromosome 12 with parental origin-dependent phenotype.
K Schuster-Gossler, D Simon-Chazottes, J L Guenet, J Zachgo, A Gossler. Mamm Genome 1996
63
20

DNA Methylation in the Diagnosis of Monogenic Diseases.
Flavia Cerrato, Angela Sparago, Francesca Ariani, Fulvia Brugnoletti, Luciano Calzari, Fabio Coppedè, Alessandro De Luca, Cristina Gervasini, Emiliano Giardina, Fiorella Gurrieri,[...]. Genes (Basel) 2020
12
20

Human imprinting disorders: Principles, practice, problems and progress.
Deborah J G Mackay, I Karen Temple. Eur J Med Genet 2017
22
20

Temple syndrome in a patient with variably methylated CpGs at the primary MEG3/DLK1:IG-DMR and severely hypomethylated CpGs at the secondary MEG3:TSS-DMR.
Masayo Kagami, Atsuhiro Yanagisawa, Miyuki Ota, Kentaro Matsuoka, Akie Nakamura, Keiko Matsubara, Kazuhiko Nakabayashi, Shuji Takada, Maki Fukami, Tsutomu Ogata. Clin Epigenetics 2019
7
20

Trisomy rescue mechanism: the case of concomitant mosaic trisomy 14 and maternal uniparental disomy 14 in a 15-year-old girl.
Samuel Balbeur, Bernard Grisart, Benoit Parmentier, Daniel Sartenaer, Pierre-Emmanuel Leonard, Urielle Ullmann, Sébastien Boulanger, Luc Leroy, Placide Ngendahayo, Constantin Lungu-Silviu,[...]. Clin Case Rep 2016
12
20

Mice lacking paternally expressed Pref-1/Dlk1 display growth retardation and accelerated adiposity.
Yang Soo Moon, Cynthia M Smas, Kichoon Lee, Josep A Villena, Kee-Hong Kim, Eun Jun Yun, Hei Sook Sul. Mol Cell Biol 2002
326
20

Epigenetic analysis of the Dlk1-Gtl2 imprinted domain on mouse chromosome 12: implications for imprinting control from comparison with Igf2-H19.
Shuji Takada, Martina Paulsen, Maxine Tevendale, Chen-En Tsai, Gavin Kelsey, Bruce M Cattanach, Anne C Ferguson-Smith. Hum Mol Genet 2002
191
20

Identification of an imprinted gene, Meg3/Gtl2 and its human homologue MEG3, first mapped on mouse distal chromosome 12 and human chromosome 14q.
N Miyoshi, H Wagatsuma, S Wakana, T Shiroishi, M Nomura, K Aisaka, T Kohda, M A Surani, T Kaneko-Ishino, F Ishino. Genes Cells 2000
281
20

Maternal uniparental disomy for chromosome 14.
I K Temple, A Cockwell, T Hassold, D Pettay, P Jacobs. J Med Genet 1991
143
20

Temple syndrome as a differential diagnosis to Prader-Willi syndrome: Identifying three new patients.
Asgeir Lande, Mette Kroken, Kai Rabben, Lars Retterstøl. Am J Med Genet A 2018
5
20

Mosaic upd(14)pat in a patient with mild features of Kagami-Ogata syndrome.
Marte G Haug, Atle Brendehaug, Gunnar Houge, Masayo Kagami, Tsutomu Ogata. Clin Case Rep 2017
6
20

Methylation analysis of the intergenic differentially methylated region of DLK1-GTL2 in human.
Elke Geuns, Nele De Temmerman, Pierre Hilven, André Van Steirteghem, Inge Liebaers, Martine De Rycke. Eur J Hum Genet 2007
45
20

Maternal Uniparental Disomy 14 (Temple Syndrome) as a Result of a Robertsonian Translocation.
Veronica Bertini, Antonella Fogli, Rossella Bruno, Alessia Azzarà, Angela Michelucci, Teresa Mattina, Silvano Bertelloni, Angelo Valetto. Mol Syndromol 2017
7
20

Kagami-Ogata syndrome in a fetus presenting with polyhydramnios, malformations, and preterm delivery: a case report.
Haipeng Huang, Yukiko Mikami, Kosuke Shigematsu, Nozomi Uemura, Mamiko Shinsaka, Ayaka Iwatani, Fumihito Miyake, Kazuhiko Kabe, Yasushi Takai, Masahiro Saitoh,[...]. J Med Case Rep 2019
2
50

Activation of paternally expressed genes and perinatal death caused by deletion of the Gtl2 gene.
Yunli Zhou, Pornsuk Cheunsuchon, Yuki Nakayama, Michael W Lawlor, Ying Zhong, Kimberley A Rice, Li Zhang, Xun Zhang, Francesca E Gordon, Hart G W Lidov,[...]. Development 2010
96
20

miRMap: Profiling 14q32 microRNA Expression and DNA Methylation Throughout the Human Vasculature.
Eveline A C Goossens, Margreet R de Vries, Karin H Simons, Hein Putter, Paul H A Quax, A Yaël Nossent. Front Cardiovasc Med 2019
8
20

The IG-DMR and the MEG3-DMR at human chromosome 14q32.2: hierarchical interaction and distinct functional properties as imprinting control centers.
Masayo Kagami, Maureen J O'Sullivan, Andrew J Green, Yoshiyuki Watabe, Osamu Arisaka, Nobuhide Masawa, Kentarou Matsuoka, Maki Fukami, Keiko Matsubara, Fumiko Kato,[...]. PLoS Genet 2010
152
20

The differentially methylated region of MEG8 is hypermethylated in patients with Temple syndrome.
Susanne Bens, Julia Kolarova, Gabriele Gillessen-Kaesbach, Karin Buiting, Jasmin Beygo, Almuth Caliebe, Ole Ammerpohl, Reiner Siebert. Epigenomics 2015
12
20

A Male Case of Kagami-Ogata Syndrome Caused by Paternal Unipaternal Disomy 14 as a Result of a Robertsonian Translocation.
Xiaoxue Wang, Hui Pang, Birju A Shah, Hongcang Gu, Lijun Zhang, Hua Wang. Front Pediatr 2020
2
50

Deletion of Gtl2, imprinted non-coding RNA, with its differentially methylated region induces lethal parent-origin-dependent defects in mice.
Nozomi Takahashi, Akira Okamoto, Ryota Kobayashi, Motomu Shirai, Yayoi Obata, Hidehiko Ogawa, Yusuke Sotomaru, Tomohiro Kono. Hum Mol Genet 2009
79
20

A tandem repeat array in IG-DMR is essential for imprinting of paternal allele at the Dlk1-Dio3 domain during embryonic development.
Takeshi Saito, Satoshi Hara, Tomoko Kato, Moe Tamano, Akari Muramatsu, Hiroshi Asahara, Shuji Takada. Hum Mol Genet 2018
9
20

New insights into the imprinted MEG8-DMR in 14q32 and clinical and molecular description of novel patients with Temple syndrome.
Jasmin Beygo, Alma Küchler, Gabriele Gillessen-Kaesbach, Beate Albrecht, Jonas Eckle, Thomas Eggermann, Alexandra Gellhaus, Deniz Kanber, Ulrike Kordaß, Hermann-Josef Lüdecke,[...]. Eur J Hum Genet 2017
18
20

Role of retrotransposon-derived imprinted gene, Rtl1, in the feto-maternal interface of mouse placenta.
Yoichi Sekita, Hirotaka Wagatsuma, Kenji Nakamura, Ryuichi Ono, Masayo Kagami, Noriko Wakisaka, Toshiaki Hino, Rika Suzuki-Migishima, Takashi Kohda, Atsuo Ogura,[...]. Nat Genet 2008
203
20

Familial Kagami-Ogata syndrome in Chinese.
Ho-Ming Luk. Clin Dysmorphol 2017
3
33

The microRNAs within the DLK1-DIO3 genomic region: involvement in disease pathogenesis.
Leonidas Benetatos, Eleftheria Hatzimichael, Eric Londin, George Vartholomatos, Phillipe Loher, Isidore Rigoutsos, Evangelos Briasoulis. Cell Mol Life Sci 2013
177
20


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.