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- Nature Genetics is a peer-reviewed scientific journal published by Nature Portfolio. It was established in 1992. It covers research in genetics. The chief...3 KB (150 words) - 10:48, 24 June 2024
- cause growth failure in idiopathic short stature and Turner syndrome". Nature Genetics. 16 (1): 54–63. doi:10.1038/ng0597-54. PMID 9140395. S2CID 26248561...11 KB (1,240 words) - 08:49, 4 January 2024
MC4R is associated with waist circumference and insulin resistance". Nature Genetics. 40 (6): 716–8. doi:10.1038/ng.156. PMID 18454146. S2CID 12331736....33 KB (3,164 words) - 08:06, 10 March 2024
"Many sequence variants affecting diversity of adult human height". Nature Genetics. 40 (5): 609–15. doi:10.1038/ng.122. PMID 18391951. S2CID 3005450....15 KB (1,572 words) - 02:00, 3 December 2023
" Nature Genetics (subscription required), Volume 31, pp 241–247, 10 June 2002 A Kong et al., "Reproduction rate and reproductive success," Nature Genetics...103 KB (12,457 words) - 23:46, 12 June 2024- Genome Research ranks 2nd in the category 'Genetics and Genomics' after Nature Genetics. The focus of the journal is on research that provides novel insights...3 KB (190 words) - 10:49, 24 June 2024
required for primary cilia formation and left-right axis specification". Nature Genetics. 38 (1): 112–117. doi:10.1038/ng1684. PMID 16311594. S2CID 2441702...12 KB (1,204 words) - 14:44, 23 August 2023
"Loss-of-function mutations in SLC30A8 protect against type 2 diabetes". Nature Genetics. 46 (4): 357–363. doi:10.1038/ng.2915. PMC 4051628. PMID 24584071....7 KB (920 words) - 16:23, 26 November 2023- cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome". Nature Genetics. 39 (7): 875–81. doi:10.1038/ng2039. PMID 17558409. S2CID 6982566....9 KB (952 words) - 03:31, 10 May 2024
[corrected] cause limb and cardiac malformation in Holt-Oram syndrome". Nature Genetics. 15 (1): 30–35. doi:10.1038/ng0197-30. PMID 8988165. S2CID 30763654...21 KB (2,467 words) - 22:17, 30 March 2024
1992). "The human PAX6 gene is mutated in two patients with aniridia". Nature Genetics. 1 (5): 328–32. doi:10.1038/ng0892-328. PMID 1302030. S2CID 13736351...22 KB (2,710 words) - 15:03, 21 December 2023
caused by mutations in a putative sulphate transporter gene (PDS)". Nature Genetics. 17 (4): 411–422. doi:10.1038/ng1297-411. PMID 9398842. S2CID 39359838...20 KB (2,317 words) - 03:49, 30 June 2024
alpha-subunit of the cone photoreceptor cGMP-gated cation channel". Nature Genetics. 19 (3): 257–9. doi:10.1038/935. PMID 9662398. S2CID 12040233. Lam...9 KB (971 words) - 16:44, 27 December 2023
in NBEAL2, encoding a BEACH protein, cause gray platelet syndrome". Nature Genetics. 43 (8): 738–40. doi:10.1038/ng.884. PMC 6050511. PMID 21765413. "OMIM...11 KB (1,052 words) - 08:24, 25 September 2022
in genome-wide mutation rates within and between human families". Nature Genetics. 43 (7): 712–4. doi:10.1038/ng.862. PMC 3322360. PMID 21666693. Ackermann...102 KB (11,019 words) - 01:56, 17 June 2024
that are associated with susceptibility to myocardial infarction". Nature Genetics. 32 (4): 650–4. doi:10.1038/ng1047. PMID 12426569. S2CID 21414260....69 KB (6,790 words) - 03:14, 15 July 2024
localization of seven PAX genes and cloning of a novel family member, PAX-9". Nature Genetics. 3 (4): 292–8. doi:10.1038/ng0493-292. PMID 7981748. S2CID 21338655...12 KB (1,473 words) - 23:39, 5 June 2024
the function of primary cilia and left-right axis determination". Nature Genetics. 34 (4): 413–20. doi:10.1038/ng1217. PMC 3732175. PMID 12872123. Konrad...10 KB (1,198 words) - 23:32, 11 April 2024
with isolated vitamin E deficiency with Michel Koenig (Ouahchi et al, Nature Genetics, 1995), Coffin-Lowry syndrome (mental retardation linked to chromosome...15 KB (1,981 words) - 21:02, 28 January 2024
the CRX homeobox gene associated with Leber congenital amaurosis". Nature Genetics. 18 (4): 311–2. doi:10.1038/ng0498-311. PMID 9537410. S2CID 22131800...12 KB (1,411 words) - 01:59, 19 July 2024
- of the expression constitutes the recognition of its metaphorical nature. (genetics) A process wherein RNA transcription is increased by a coactivator
- Genetics, and Health at the Dawn of the Genome Era" (November 2004), Nature Genetics Supplement, vol. 36, no. 11 Vibrant human diversity is now commonplace
- 2009. Repeatability of published microarray gene expression analyses. Nature Genetics 41(2): 149–155 DOI 10.1038/ng.295 Mooney H, Newton MP. 2012. The anatomy
- Kurotaki et al., Haploinsufficiency of NSD1 causes Sotos syndrome (2002) Nature Genetics, 30: 365-366 Management of Genetic Syndromes. Edited by S.B. Cassidy