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Items: 1 to 20 of 96

1.

A genome-wide association scan implicates DCHS2, RUNX2, GLI3, PAX1 and EDAR in human facial variation.

Adhikari K, Fuentes-Guajardo M, Quinto-Sánchez M, Mendoza-Revilla J, Camilo Chacón-Duque J, Acuña-Alonzo V, Jaramillo C, Arias W, Lozano RB, Pérez GM, Gómez-Valdés J, Villamil-Ramírez H, Hunemeier T, Ramallo V, Silva de Cerqueira CC, Hurtado M, Villegas V, Granja V, Gallo C, Poletti G, Schuler-Faccini L, Salzano FM, Bortolini MC, Canizales-Quinteros S, Cheeseman M, Rosique J, Bedoya G, Rothhammer F, Headon D, González-José R, Balding D, Ruiz-Linares A.

Nat Commun. 2016 May 19;7:11616. doi: 10.1038/ncomms11616.

2.

A genome-wide association study identifies multiple loci for variation in human ear morphology.

Adhikari K, Reales G, Smith AJ, Konka E, Palmen J, Quinto-Sanchez M, Acuña-Alonzo V, Jaramillo C, Arias W, Fuentes M, Pizarro M, Barquera Lozano R, Macín Pérez G, Gómez-Valdés J, Villamil-Ramírez H, Hunemeier T, Ramallo V, Silva de Cerqueira CC, Hurtado M, Villegas V, Granja V, Gallo C, Poletti G, Schuler-Faccini L, Salzano FM, Bortolini MC, Canizales-Quinteros S, Rothhammer F, Bedoya G, Calderón R, Rosique J, Cheeseman M, Bhutta MF, Humphries SE, Gonzalez-José R, Headon D, Balding D, Ruiz-Linares A.

Nat Commun. 2015 Jun 24;6:7500. doi: 10.1038/ncomms8500.

3.

Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology.

Shaffer JR, Orlova E, Lee MK, Leslie EJ, Raffensperger ZD, Heike CL, Cunningham ML, Hecht JT, Kau CH, Nidey NL, Moreno LM, Wehby GL, Murray JC, Laurie CA, Laurie CC, Cole J, Ferrara T, Santorico S, Klein O, Mio W, Feingold E, Hallgrimsson B, Spritz RA, Marazita ML, Weinberg SM.

PLoS Genet. 2016 Aug 25;12(8):e1006149. doi: 10.1371/journal.pgen.1006149. eCollection 2016 Aug.

4.

Genome-wide association study of three-dimensional facial morphology identifies a variant in PAX3 associated with nasion position.

Paternoster L, Zhurov AI, Toma AM, Kemp JP, St Pourcain B, Timpson NJ, McMahon G, McArdle W, Ring SM, Smith GD, Richmond S, Evans DM.

Am J Hum Genet. 2012 Mar 9;90(3):478-85. doi: 10.1016/j.ajhg.2011.12.021. Epub 2012 Feb 16.

5.

A genome-wide association study identifies five loci influencing facial morphology in Europeans.

Liu F, van der Lijn F, Schurmann C, Zhu G, Chakravarty MM, Hysi PG, Wollstein A, Lao O, de Bruijne M, Ikram MA, van der Lugt A, Rivadeneira F, Uitterlinden AG, Hofman A, Niessen WJ, Homuth G, de Zubicaray G, McMahon KL, Thompson PM, Daboul A, Puls R, Hegenscheid K, Bevan L, Pausova Z, Medland SE, Montgomery GW, Wright MJ, Wicking C, Boehringer S, Spector TD, Paus T, Martin NG, Biffar R, Kayser M.

PLoS Genet. 2012 Sep;8(9):e1002932. doi: 10.1371/journal.pgen.1002932. Epub 2012 Sep 13.

6.

[The effect of EDARV370A on facial and ear morphologies in Uyghur population].

Li Y, Zhao WT, Li D, Tao XM, Xiong ZY, Liu J, Zhang W, Liu HB, Ji AQ, Tang K, Liu F, Li CX.

Yi Chuan. 2018 Nov 20;40(11):1024-1032. doi: 10.16288/j.yczz.18-268. Chinese.

PMID:
30465535
7.

Genome-wide scans reveal variants at EDAR predominantly affecting hair straightness in Han Chinese and Uyghur populations.

Wu S, Tan J, Yang Y, Peng Q, Zhang M, Li J, Lu D, Liu Y, Lou H, Feng Q, Lu Y, Guan Y, Zhang Z, Jiao Y, Sabeti P, Krutmann J, Tang K, Jin L, Xu S, Wang S.

Hum Genet. 2016 Nov;135(11):1279-1286. Epub 2016 Aug 3.

PMID:
27487801
8.

Association between EDAR Polymorphisms and Non-Syndromic Tooth Agenesis in the Chinese Han Population.

Chen YT, Liu HC, Han D, Liu Y, Feng HL.

Chin J Dent Res. 2017;20(3):153-159. doi: 10.3290/j.cjdr.a38770.

9.

The association study of nonsyndromic cleft lip with or without cleft palate identified risk variants of the GLI3 gene in a Chinese population.

Wang Y, Sun Y, Huang Y, Pan Y, Shi B, Ma J, Ma L, Lan F, Zhou Y, Shi J, Zhu J, Jiang H, Zhang L, Xiao X, Jiang M, Yin A, Yu L, Wang L, Cheng J, Yang Y.

J Genet. 2017 Sep;96(4):687-693.

10.

Prevention of premature fusion of calvarial suture in GLI-Kruppel family member 3 (Gli3)-deficient mice by removing one allele of Runt-related transcription factor 2 (Runx2).

Tanimoto Y, Veistinen L, Alakurtti K, Takatalo M, Rice DP.

J Biol Chem. 2012 Jun 15;287(25):21429-38. doi: 10.1074/jbc.M112.362145. Epub 2012 Apr 30.

11.

Calcium Signaling Pathway Genes RUNX2 and CACNA1C Are Associated With Calcific Aortic Valve Disease.

Guauque-Olarte S, Messika-Zeitoun D, Droit A, Lamontagne M, Tremblay-Marchand J, Lavoie-Charland E, Gaudreault N, Arsenault BJ, Dubé MP, Tardif JC, Body SC, Seidman JG, Boileau C, Mathieu P, Pibarot P, Bossé Y.

Circ Cardiovasc Genet. 2015 Dec;8(6):812-22. doi: 10.1161/CIRCGENETICS.115.001145. Epub 2015 Nov 9.

12.

Genetic determination of human facial morphology: links between cleft-lips and normal variation.

Boehringer S, van der Lijn F, Liu F, Günther M, Sinigerova S, Nowak S, Ludwig KU, Herberz R, Klein S, Hofman A, Uitterlinden AG, Niessen WJ, Breteler MM, van der Lugt A, Würtz RP, Nöthen MM, Horsthemke B, Wieczorek D, Mangold E, Kayser M.

Eur J Hum Genet. 2011 Nov;19(11):1192-7. doi: 10.1038/ejhg.2011.110. Epub 2011 Jun 22.

13.

Genomewide Association Study of African Children Identifies Association of SCHIP1 and PDE8A with Facial Size and Shape.

Cole JB, Manyama M, Kimwaga E, Mathayo J, Larson JR, Liberton DK, Lukowiak K, Ferrara TM, Riccardi SL, Li M, Mio W, Prochazkova M, Williams T, Li H, Jones KL, Klein OD, Santorico SA, Hallgrimsson B, Spritz RA.

PLoS Genet. 2016 Aug 25;12(8):e1006174. doi: 10.1371/journal.pgen.1006174. eCollection 2016 Aug.

14.

Genome-wide association study and admixture mapping reveal new loci associated with total IgE levels in Latinos.

Pino-Yanes M, Gignoux CR, Galanter JM, Levin AM, Campbell CD, Eng C, Huntsman S, Nishimura KK, Gourraud PA, Mohajeri K, O'Roak BJ, Hu D, Mathias RA, Nguyen EA, Roth LA, Padhukasahasram B, Moreno-Estrada A, Sandoval K, Winkler CA, Lurmann F, Davis A, Farber HJ, Meade K, Avila PC, Serebrisky D, Chapela R, Ford JG, Lenoir MA, Thyne SM, Brigino-Buenaventura E, Borrell LN, Rodriguez-Cintron W, Sen S, Kumar R, Rodriguez-Santana JR, Bustamante CD, Martinez FD, Raby BA, Weiss ST, Nicolae DL, Ober C, Meyers DA, Bleecker ER, Mack SJ, Hernandez RD, Eichler EE, Barnes KC, Williams LK, Torgerson DG, Burchard EG.

J Allergy Clin Immunol. 2015 Jun;135(6):1502-10. doi: 10.1016/j.jaci.2014.10.033. Epub 2014 Dec 6.

15.

A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females.

Sharma S, Londono D, Eckalbar WL, Gao X, Zhang D, Mauldin K, Kou I, Takahashi A, Matsumoto M, Kamiya N, Murphy KK, Cornelia R; TSRHC Scoliosis Clinical Group; Japan Scoliosis Clinical Research Group, Herring JA, Burns D, Ahituv N, Ikegawa S, Gordon D, Wise CA.

Nat Commun. 2015 Mar 18;6:6452. doi: 10.1038/ncomms7452.

16.

Effects of an Asian-specific nonsynonymous EDAR variant on multiple dental traits.

Park JH, Yamaguchi T, Watanabe C, Kawaguchi A, Haneji K, Takeda M, Kim YI, Tomoyasu Y, Watanabe M, Oota H, Hanihara T, Ishida H, Maki K, Park SB, Kimura R.

J Hum Genet. 2012 Aug;57(8):508-14. doi: 10.1038/jhg.2012.60. Epub 2012 May 31.

PMID:
22648185
17.

Evolutionary significance of selected EDAR variants in Tibetan high-altitude adaptations.

Shao J, Raza MS, Zhuoma B, Zeng C.

Sci China Life Sci. 2018 Jan;61(1):68-78. doi: 10.1007/s11427-016-9045-7. Epub 2017 Aug 8.

PMID:
28795375
18.

Developmental pathways inferred from modularity, morphological integration and fluctuating asymmetry patterns in the human face.

Quinto-Sánchez M, Muñoz-Muñoz F, Gomez-Valdes J, Cintas C, Navarro P, Cerqueira CCS, Paschetta C, de Azevedo S, Ramallo V, Acuña-Alonzo V, Adhikari K, Fuentes-Guajardo M, Hünemeier T, Everardo P, de Avila F, Jaramillo C, Arias W, Gallo C, Poletti G, Bedoya G, Bortolini MC, Canizales-Quinteros S, Rothhammer F, Rosique J, Ruiz-Linares A, Gonzalez-Jose R.

Sci Rep. 2018 Jan 17;8(1):963. doi: 10.1038/s41598-018-19324-y.

19.

Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2.

Lee MK, Shaffer JR, Leslie EJ, Orlova E, Carlson JC, Feingold E, Marazita ML, Weinberg SM.

PLoS One. 2017 Apr 25;12(4):e0176566. doi: 10.1371/journal.pone.0176566. eCollection 2017.

20.

A genome-wide association scan for acute insulin response to glucose in Hispanic-Americans: the Insulin Resistance Atherosclerosis Family Study (IRAS FS).

Rich SS, Goodarzi MO, Palmer ND, Langefeld CD, Ziegler J, Haffner SM, Bryer-Ash M, Norris JM, Taylor KD, Haritunians T, Rotter JI, Chen YD, Wagenknecht LE, Bowden DW, Bergman RN.

Diabetologia. 2009 Jul;52(7):1326-33. doi: 10.1007/s00125-009-1373-0. Epub 2009 May 9.

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