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Genetic Syndromes and Imprinting

TopicLeading institutions, researchers & key papers

Genetic Syndromes and Imprinting is a topic indexed in ScholarIQ from OpenAlex.

What is known about Genetic Syndromes and Imprinting?

ScholarIQrecord summary

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.

How many works does Genetic Syndromes and Imprinting have?

ScholarIQindexed works

Genetic Syndromes and Imprinting has 226 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

What is the OpenAlex record for Genetic Syndromes and Imprinting?

ScholarIQopenalex

The OpenAlex for Genetic Syndromes and Imprinting is on the source record.

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
Nature Genetics. 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
Nature Genetics. 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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