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Genetic Syndromes and Imprinting
TopicLeading institutions, researchers & key papers
This cluster of papers explores the phenomenon of genomic imprinting, where certain genes are expressed in a parent-of-origin-specific manner. It covers topics such as parental influence on gene expression, epigenetic regulation through DNA methylation, and the role of imprinted genes in syndromes like Prader-Willi and Angelman. Additionally, it delves into the mechanisms of imprint control regions and the involvement of non-coding RNA in regulating imprinted gene networks.
226
Works
IDs:OpenAlex
How has Genetic Syndromes and Imprinting's publication output changed over time?
ScholarIQpublication output · 2002–2018
Output declined50% over the shown period — from 2 works in 2002 to 1 in 2018.
2
2
1
2
1
1
1
1
1
1
2002200320062007200820092010201520162018
What are the most-cited papers on Genetic Syndromes and Imprinting?
ScholarIQmost cited works
Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour
Osamu Ogawa, Michael R. Eccles, Jenny Szeto, Leslie A. McNoe, Kankatsu Yun, Marion A. Maw, Peter J. Smith, A E Reeve
Nature. 1993709 Citations
Haploinsufficiency of NSD1 causes Sotos syndrome
Naohiro Kurotaki, Kiyoshi Imaizumi, Naoki Harada, Mitsuo Masuno, Tatsuro Kondoh, Toshiro Nagai, Hirofumi Ohashi, Kenji Naritomi, Masato Tsukahara, Yoshio Makita, Tateo Sugimoto, Tohru Sonoda, Tomoko Hasegawa, Yasuaki Chinen, Hiroaki Tomita, Akira Kinoshita, Tsuyoshi Mizuguchi, Koh-ichiro Yoshiura, Tohru Ohta, Tatsuya Kishino, Yoshimitsu Fukushima, Norio Niikawa, Naomichi Matsumoto
S137905309. 2002660 Citations
A Pituitary-Derived MEG3 Isoform Functions as a Growth Suppressor in Tumor Cells
Xun Zhang, Yunli Zhou, Kshama Mehta, Daniel C. Danila, Staci Scolavino, Stacey R. Johnson, Anne Klibanski
The Journal of Clinical Endocrinology & Metabolism. 2003449 CitationsOPEN ACCESS
CTCF Mediates Interchromosomal Colocalization Between <i>Igf2/H19</i> and <i>Wsb1/Nf1</i>
Jian Qun Ling, Tao Li, Ji‐Fan Hu, Thanh Vu, Huiling Chen, Xin Wen Qiu, Athena M. Cherry, Andrew R. Hoffman
Science. 2006432 Citations
An imprinted gene p57KIP2 is mutated in Beckwith–Wiedemann syndrome
Izuho Hatada, Hirofumi Ohashi, Yoshimitsu Fukushima, Yasuhiko Kaneko, Masahiro Inoue, Yosuke Komoto, Akira Okada, Sachiko Oh‐ishi, Akira Nabetani, Hiroko Morisaki, Masahiro Nakayama, Norio Niikawa, Tsunehiro Mukai
S137905309. 1996385 Citations
Where is Genetic Syndromes and Imprinting research published, and who funds it?
ScholarIQvenues & funding sources
TOP FUNDERS
National Science Foundation—
NIH—
Wellcome Trust—
European Research Council—
Funder breakdown is a member featureSign up free to unlock
How much of the research on Genetic Syndromes and Imprinting is open access?
ScholarIQopen access share
67%OPEN ACCESS
Gold
0%
Green
7%
Hybrid
13%
Bronze
47%
Closed
33%
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