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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1978 1
1983 2
1987 2
1989 1
1990 1
1991 2
1992 1
1993 1
1994 2
1997 1
1998 5
1999 1
2000 2
2001 2
2002 3
2003 4
2004 6
2005 2
2006 10
2007 12
2008 3
2009 9
2010 10
2011 6
2012 7
2013 4
2014 10
2015 3
2016 3
2017 5
2018 2
2019 4
2020 1
2021 2
2022 3
2023 1
2024 2

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125 results

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Page 1
Aberrant expression of agouti signaling protein (ASIP) as a cause of monogenic severe childhood obesity.
Kempf E, Landgraf K, Stein R, Hanschkow M, Hilbert A, Abou Jamra R, Boczki P, Herberth G, Kühnapfel A, Tseng YH, Stäubert C, Schöneberg T, Kühnen P, Rayner NW, Zeggini E, Kiess W, Blüher M, Körner A. Kempf E, et al. Nat Metab. 2022 Dec;4(12):1697-1712. doi: 10.1038/s42255-022-00703-9. Epub 2022 Dec 19. Nat Metab. 2022. PMID: 36536132 Free PMC article.
The mutation places ASIP under control of the ubiquitously active itchy E3 ubiquitin protein ligase promoter, driving the generation of ASIP in patient-derived native and induced pluripotent stem cells for all germ layers and hypothalamic-like neurons. The patient's phenotype of …
The mutation places ASIP under control of the ubiquitously active itchy E3 ubiquitin protein ligase promoter, driving the generation of ASIP …
Melanoma risk prediction models.
Nikolić J, Loncar-Turukalo T, Sladojević S, Marinković M, Janjić Z. Nikolić J, et al. Vojnosanit Pregl. 2014 Aug;71(8):757-66. doi: 10.2298/vsp130722045n. Vojnosanit Pregl. 2014. PMID: 25181836
Red hair, phototype I and large congenital naevi were only present in melanoma patients and thus were strongly associated with melanoma. ...CONCLUSION: Application of different models for risk assessment and prediction of melanoma should provide efficient and
Red hair, phototype I and large congenital naevi were only present in melanoma patients and thus were strongly associated with
Pigmented lesions in children: when to worry.
Schaffer JV. Schaffer JV. Curr Opin Pediatr. 2007 Aug;19(4):430-40. doi: 10.1097/MOP.0b013e32825b0788. Curr Opin Pediatr. 2007. PMID: 17630608 Review.
This review summarizes the types of melanocytic nevi that are commonly observed in children, environmental (e.g. sun exposure) and genetic (e.g. the familial atypical mole and melanoma syndrome) factors that can contribute to the development of nevi and future risk of mela …
This review summarizes the types of melanocytic nevi that are commonly observed in children, environmental (e.g. sun exposure) and ge …
Accuracy of Eye and Hair Color Prediction in Mexican Mestizos from Monterrey City Based on ForenSeq(TM) DNA Signature Prep.
Aguilar-Velázquez JA, Llamas-de-Dios BJ, Córdova-Mercado MF, Coronado-Ávila CE, Salas-Salas O, López-Quintero A, Ramos-González B, Rangel-Villalobos H. Aguilar-Velázquez JA, et al. Genes (Basel). 2023 May 22;14(5):1120. doi: 10.3390/genes14051120. Genes (Basel). 2023. PMID: 37239480 Free PMC article.
We observed predominantly brown eyes (96.5%) and black hair (75%) phenotypes, whereas blue eyes, and blond and red hair were not observed. Both UAS and EMC showed high performance in eye color prediction (p 96.6%), but a lower accuracy was ob
We observed predominantly brown eyes (96.5%) and black hair (75%) phenotypes, whereas blue eyes, and blond and red hair
Diversity of human hair pigmentation as studied by chemical analysis of eumelanin and pheomelanin.
Ito S, Wakamatsu K. Ito S, et al. J Eur Acad Dermatol Venereol. 2011 Dec;25(12):1369-80. doi: 10.1111/j.1468-3083.2011.04278.x. J Eur Acad Dermatol Venereol. 2011. PMID: 22077870 Review.
Eumelanin contents decrease in that order, with a trace but constant level of pheomelanin, except for red hair which contains about equal levels of pheomelanin and eumelanin. ...The genotype of melanocortin-1 receptor (MC1R), a gene regulating the red hair
Eumelanin contents decrease in that order, with a trace but constant level of pheomelanin, except for red hair which contains …
What is the connection between red hair and Tourette syndrome?
Sterling-Levis K, Williams K. Sterling-Levis K, et al. Med Hypotheses. 2009 Nov;73(5):849-53. doi: 10.1016/j.mehy.2009.03.052. Epub 2009 May 30. Med Hypotheses. 2009. PMID: 19482440
Tourette syndrome occurs worldwide and the clinical features are similar irrespective of the country of origin, with genetic causes suspected, but to date not proven. A link between red hair colour and Tourette syndrome has been hypothesised as a result of an obs
Tourette syndrome occurs worldwide and the clinical features are similar irrespective of the country of origin, with genetic causes suspecte …
DNA-based predictive models for the presence of freckles.
Kukla-Bartoszek M, Pośpiech E, Woźniak A, Boroń M, Karłowska-Pik J, Teisseyre P, Zubańska M, Bronikowska A, Grzybowski T, Płoski R, Spólnicka M, Branicki W. Kukla-Bartoszek M, et al. Forensic Sci Int Genet. 2019 Sep;42:252-259. doi: 10.1016/j.fsigen.2019.07.012. Epub 2019 Jul 30. Forensic Sci Int Genet. 2019. PMID: 31400656 Free article.
Freckles are especially common in people with pale skin and red hair and therefore it is expected that predisposition to freckles may partially share the genetic background with other pigmentation traits. ...Prediction accuracy of the intermediate category wa …
Freckles are especially common in people with pale skin and red hair and therefore it is expected that predisposition to freck …
Genome-Wide Association Shows that Pigmentation Genes Play a Role in Skin Aging.
Law MH, Medland SE, Zhu G, Yazar S, Viñuela A, Wallace L, Shekar SN, Duffy DL, Bataille V, Glass D, Spector TD, Wood D; MuTHER Consortium; Gordon SD, Barbour JM, Henders AK, Hewitt AW, Montgomery GW, Sturm RA, Mackey DA, Green AC, Martin NG, MacGregor S. Law MH, et al. J Invest Dermatol. 2017 Sep;137(9):1887-1894. doi: 10.1016/j.jid.2017.04.026. Epub 2017 May 11. J Invest Dermatol. 2017. PMID: 28502801 Free article. Review.
At all three loci we highlight putative functionally relevant SNPs. There are a number of red hair/low pigmentation alleles of MC1R; we found that together these MC1R alleles explained 4.1% of variance in skin pattern damage. We also show that skin aging and reporte …
At all three loci we highlight putative functionally relevant SNPs. There are a number of red hair/low pigmentation alleles of …
Influence of germline genetic variants on dermoscopic features of melanoma.
Pozzobon FC, Tell-Marti G, Calbet-Llopart N, Barreiro A, Espinosa N, Potrony M, Alejo B, Podlipnik S, Combalia M, Puig-Butillé JA, Carrera C, Malvehy J, Puig S. Pozzobon FC, et al. Pigment Cell Melanoma Res. 2021 May;34(3):618-628. doi: 10.1111/pcmr.12954. Epub 2021 Jan 31. Pigment Cell Melanoma Res. 2021. PMID: 33342058
SNPs of PLA2G6 (rs132985), PAX3 (rs7600206), and IRF4 (rs12203592) genes were also associated with either shiny white structures or mixed regression (all corrected p-values .06). Melanomas from red hair color MC1R variants carriers showed lower total dermoscopy s
SNPs of PLA2G6 (rs132985), PAX3 (rs7600206), and IRF4 (rs12203592) genes were also associated with either shiny white structures or mixed re …
Estimating the attributable fraction for melanoma: a meta-analysis of pigmentary characteristics and freckling.
Olsen CM, Carroll HJ, Whiteman DC. Olsen CM, et al. Int J Cancer. 2010 Nov 15;127(10):2430-45. doi: 10.1002/ijc.25243. Int J Cancer. 2010. PMID: 20143394 Free article. Review.
IV); and 1.99 for presence of freckling. The highest PAFs were observed for skin phototypes 1/II (0.27), presence of freckling (0.23), and blond hair colour (0.23). For eye colour, the PAF for blue/blue-grey eye colour was higher than for green/grey/hazel eye colour (0.18 …
IV); and 1.99 for presence of freckling. The highest PAFs were observed for skin phototypes 1/II (0.27), presence of freckling (0.23) …
125 results