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Results: 1 to 20 of 106

1.

Improved phylogenetic resolution and rapid diversification of Y-chromosome haplogroup K-M526 in Southeast Asia.

Karafet TM, Mendez FL, Sudoyo H, Lansing JS, Hammer MF.

Eur J Hum Genet. 2014 Jun 4. doi: 10.1038/ejhg.2014.106. [Epub ahead of print]

PMID:
24896152
[PubMed - as supplied by publisher]
2.

A novel de novo mutation of SCN8A (Nav1.6) with enhanced channel activation in a child with epileptic encephalopathy.

Estacion M, O'Brien JE, Conravey A, Hammer MF, Waxman SG, Dib-Hajj SD, Meisler MH.

Neurobiol Dis. 2014 Sep;69:117-23. doi: 10.1016/j.nbd.2014.05.017. Epub 2014 May 27.

PMID:
24874546
[PubMed - in process]
Free Article
3.

Evidence for Increased Levels of Positive and Negative Selection on the X Chromosome versus Autosomes in Humans.

Veeramah KR, Gutenkunst RN, Woerner AE, Watkins JC, Hammer MF.

Mol Biol Evol. 2014 May 15. pii: msu166. [Epub ahead of print]

PMID:
24830675
[PubMed - as supplied by publisher]
4.

The impact of whole-genome sequencing on the reconstruction of human population history.

Veeramah KR, Hammer MF.

Nat Rev Genet. 2014 Mar;15(3):149-62. doi: 10.1038/nrg3625. Epub 2014 Feb 4. Review.

PMID:
24492235
[PubMed - indexed for MEDLINE]
5.

Multistate structural modeling and voltage-clamp analysis of epilepsy/autism mutation Kv10.2-R327H demonstrate the role of this residue in stabilizing the channel closed state.

Yang Y, Vasylyev DV, Dib-Hajj F, Veeramah KR, Hammer MF, Dib-Hajj SD, Waxman SG.

J Neurosci. 2013 Oct 16;33(42):16586-93. doi: 10.1523/JNEUROSCI.2307-13.2013.

PMID:
24133262
[PubMed - indexed for MEDLINE]
Free Article
6.

Great ape genetic diversity and population history.

Prado-Martinez J, Sudmant PH, Kidd JM, Li H, Kelley JL, Lorente-Galdos B, Veeramah KR, Woerner AE, O'Connor TD, Santpere G, Cagan A, Theunert C, Casals F, Laayouni H, Munch K, Hobolth A, Halager AE, Malig M, Hernandez-Rodriguez J, Hernando-Herraez I, Prüfer K, Pybus M, Johnstone L, Lachmann M, Alkan C, Twigg D, Petit N, Baker C, Hormozdiari F, Fernandez-Callejo M, Dabad M, Wilson ML, Stevison L, Camprubí C, Carvalho T, Ruiz-Herrera A, Vives L, Mele M, Abello T, Kondova I, Bontrop RE, Pusey A, Lankester F, Kiyang JA, Bergl RA, Lonsdorf E, Myers S, Ventura M, Gagneux P, Comas D, Siegismund H, Blanc J, Agueda-Calpena L, Gut M, Fulton L, Tishkoff SA, Mullikin JC, Wilson RK, Gut IG, Gonder MK, Ryder OA, Hahn BH, Navarro A, Akey JM, Bertranpetit J, Reich D, Mailund T, Schierup MH, Hvilsom C, Andrés AM, Wall JD, Bustamante CD, Hammer MF, Eichler EE, Marques-Bonet T.

Nature. 2013 Jul 25;499(7459):471-5. doi: 10.1038/nature12228. Epub 2013 Jul 3.

PMID:
23823723
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Exome sequencing reveals new causal mutations in children with epileptic encephalopathies.

Veeramah KR, Johnstone L, Karafet TM, Wolf D, Sprissler R, Salogiannis J, Barth-Maron A, Greenberg ME, Stuhlmann T, Weinert S, Jentsch TJ, Pazzi M, Restifo LL, Talwar D, Erickson RP, Hammer MF.

Epilepsia. 2013 Jul;54(7):1270-81. doi: 10.1111/epi.12201. Epub 2013 May 3.

PMID:
23647072
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

The KCNJ8-S422L variant previously associated with J-wave syndromes is found at an increased frequency in Ashkenazi Jews.

Veeramah KR, Karafet TM, Wolf D, Samson RA, Hammer MF.

Eur J Hum Genet. 2014 Jan;22(1):94-8. doi: 10.1038/ejhg.2013.78. Epub 2013 May 1.

PMID:
23632791
[PubMed - in process]
9.

Human hybrids.

Hammer MF.

Sci Am. 2013 May;308(5):66-71. No abstract available.

PMID:
23627222
[PubMed - indexed for MEDLINE]
10.

An African American paternal lineage adds an extremely ancient root to the human Y chromosome phylogenetic tree.

Mendez FL, Krahn T, Schrack B, Krahn AM, Veeramah KR, Woerner AE, Fomine FL, Bradman N, Thomas MG, Karafet TM, Hammer MF.

Am J Hum Genet. 2013 Mar 7;92(3):454-9. doi: 10.1016/j.ajhg.2013.02.002. Epub 2013 Feb 28. Erratum in: Am J Hum Genet. 2013 Apr 4;92(4):637.

PMID:
23453668
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Higher levels of neanderthal ancestry in East Asians than in Europeans.

Wall JD, Yang MA, Jay F, Kim SK, Durand EY, Stevison LS, Gignoux C, Woerner A, Hammer MF, Slatkin M.

Genetics. 2013 May;194(1):199-209. doi: 10.1534/genetics.112.148213. Epub 2013 Feb 14.

PMID:
23410836
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

The Indonesian archipelago: an ancient genetic highway linking Asia and the Pacific.

Tumonggor MK, Karafet TM, Hallmark B, Lansing JS, Sudoyo H, Hammer MF, Cox MP.

J Hum Genet. 2013 Mar;58(3):165-73. doi: 10.1038/jhg.2012.154. Epub 2013 Jan 24.

PMID:
23344321
[PubMed - indexed for MEDLINE]
13.

Neandertal origin of genetic variation at the cluster of OAS immunity genes.

Mendez FL, Watkins JC, Hammer MF.

Mol Biol Evol. 2013 Apr;30(4):798-801. doi: 10.1093/molbev/mst004. Epub 2013 Jan 12.

PMID:
23315957
[PubMed - indexed for MEDLINE]
Free Article
14.

A high-coverage genome sequence from an archaic Denisovan individual.

Meyer M, Kircher M, Gansauge MT, Li H, Racimo F, Mallick S, Schraiber JG, Jay F, Prüfer K, de Filippo C, Sudmant PH, Alkan C, Fu Q, Do R, Rohland N, Tandon A, Siebauer M, Green RE, Bryc K, Briggs AW, Stenzel U, Dabney J, Shendure J, Kitzman J, Hammer MF, Shunkov MV, Derevianko AP, Patterson N, Andrés AM, Eichler EE, Slatkin M, Reich D, Kelso J, Pääbo S.

Science. 2012 Oct 12;338(6104):222-6. doi: 10.1126/science.1224344. Epub 2012 Aug 30.

PMID:
22936568
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

A haplotype at STAT2 Introgressed from neanderthals and serves as a candidate of positive selection in Papua New Guinea.

Mendez FL, Watkins JC, Hammer MF.

Am J Hum Genet. 2012 Aug 10;91(2):265-74. doi: 10.1016/j.ajhg.2012.06.015.

PMID:
22883142
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Religion as a means to assure paternity.

Strassmann BI, Kurapati NT, Hug BF, Burke EE, Gillespie BW, Karafet TM, Hammer MF.

Proc Natl Acad Sci U S A. 2012 Jun 19;109(25):9781-5. doi: 10.1073/pnas.1110442109. Epub 2012 Jun 4.

PMID:
22665788
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

De novo pathogenic SCN8A mutation identified by whole-genome sequencing of a family quartet affected by infantile epileptic encephalopathy and SUDEP.

Veeramah KR, O'Brien JE, Meisler MH, Cheng X, Dib-Hajj SD, Waxman SG, Talwar D, Girirajan S, Eichler EE, Restifo LL, Erickson RP, Hammer MF.

Am J Hum Genet. 2012 Mar 9;90(3):502-10. doi: 10.1016/j.ajhg.2012.01.006. Epub 2012 Feb 23.

PMID:
22365152
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Global genetic variation at OAS1 provides evidence of archaic admixture in Melanesian populations.

Mendez FL, Watkins JC, Hammer MF.

Mol Biol Evol. 2012 Jun;29(6):1513-20. doi: 10.1093/molbev/msr301. Epub 2012 Jan 16.

PMID:
22319157
[PubMed - indexed for MEDLINE]
Free Article
19.

Genetic evidence for archaic admixture in Africa.

Hammer MF, Woerner AE, Mendez FL, Watkins JC, Wall JD.

Proc Natl Acad Sci U S A. 2011 Sep 13;108(37):15123-8. doi: 10.1073/pnas.1109300108. Epub 2011 Sep 6.

PMID:
21896735
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

An early divergence of KhoeSan ancestors from those of other modern humans is supported by an ABC-based analysis of autosomal resequencing data.

Veeramah KR, Wegmann D, Woerner A, Mendez FL, Watkins JC, Destro-Bisol G, Soodyall H, Louie L, Hammer MF.

Mol Biol Evol. 2012 Feb;29(2):617-30. doi: 10.1093/molbev/msr212. Epub 2011 Sep 1.

PMID:
21890477
[PubMed - indexed for MEDLINE]
Free PMC Article

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