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Items: 1 to 20 of 328

1.

The role of phylogenetically conserved elements in shaping patterns of human genomic diversity.

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

Mol Biol Evol. 2018 Aug 3. doi: 10.1093/molbev/msy145. [Epub ahead of print]

PMID:
30113695
2.

Modeling SNP array ascertainment with Approximate Bayesian Computation for demographic inference.

Quinto-Cortés CD, Woerner AE, Watkins JC, Hammer MF.

Sci Rep. 2018 Jul 5;8(1):10209. doi: 10.1038/s41598-018-28539-y.

3.

Ectopic Fetal Hepatic Tissue in the Placenta.

Stonko DP, Liang J, Weeks AG, Redline RW, Boyd TK, Watkins JC, Kovach AE.

Int J Gynecol Pathol. 2018 Jun 12. doi: 10.1097/PGP.0000000000000531. [Epub ahead of print]

PMID:
29901524
4.

Classic Vulvar Intraepithelial Neoplasia With Superimposed Lichen Simplex Chronicus: A Unique Variant Mimicking Differentiated Vulvar Intraepithelial Neoplasia.

Watkins JC, Yang E, Crum CP, Herfs M, Gheit T, Tommasino M, Nucci MR.

Int J Gynecol Pathol. 2018 May 10. doi: 10.1097/PGP.0000000000000509. [Epub ahead of print]

PMID:
29750709
5.

Extramammary Paget Disease of the Vulva: A Case Series Examining Treatment, Recurrence, and Malignant Transformation.

Nitecki R, Davis M, Watkins JC, Wu YE, Vitonis AF, Muto MG, Berkowitz RS, Horowitz NS, Feltmate CM.

Int J Gynecol Cancer. 2018 Mar;28(3):632-638. doi: 10.1097/IGC.0000000000001189.

PMID:
29324542
6.

Neurotransmitters and Sodium Channelopathies; Possible Link?

Hammer MF, Encinas ADC.

Pediatr Neurol Briefs. 2017 Nov;31(3):7. doi: 10.15844/pedneurbriefs-31-3-1.

7.

Exome Sequencing Provides Evidence of Polygenic Adaptation to a Fat-Rich Animal Diet in Indigenous Siberian Populations.

Hsieh P, Hallmark B, Watkins J, Karafet TM, Osipova LP, Gutenkunst RN, Hammer MF.

Mol Biol Evol. 2017 Nov 1;34(11):2913-2926. doi: 10.1093/molbev/msx226.

PMID:
28962010
8.

Complex Patterns of Admixture across the Indonesian Archipelago.

Hudjashov G, Karafet TM, Lawson DJ, Downey S, Savina O, Sudoyo H, Lansing JS, Hammer MF, Cox MP.

Mol Biol Evol. 2017 Oct 1;34(10):2439-2452. doi: 10.1093/molbev/msx196.

9.

Identification of ALK Rearrangements in Malignant Peritoneal Mesothelioma.

Hung YP, Dong F, Watkins JC, Nardi V, Bueno R, Dal Cin P, Godleski JJ, Crum CP, Chirieac LR.

JAMA Oncol. 2018 Feb 1;4(2):235-238. doi: 10.1001/jamaoncol.2017.2918.

PMID:
28910456
10.

Rare variants of small effect size in neuronal excitability genes influence clinical outcome in Japanese cases of SCN1A truncation-positive Dravet syndrome.

Hammer MF, Ishii A, Johnstone L, Tchourbanov A, Lau B, Sprissler R, Hallmark B, Zhang M, Zhou J, Watkins J, Hirose S.

PLoS One. 2017 Jul 7;12(7):e0180485. doi: 10.1371/journal.pone.0180485. eCollection 2017.

11.

Clinical implications of SCN1A missense and truncation variants in a large Japanese cohort with Dravet syndrome.

Ishii A, Watkins JC, Chen D, Hirose S, Hammer MF.

Epilepsia. 2017 Feb;58(2):282-290. doi: 10.1111/epi.13639. Epub 2016 Dec 24.

12.

Altered gene expression profile in a mouse model of SCN8A encephalopathy.

Sprissler RS, Wagnon JL, Bunton-Stasyshyn RK, Meisler MH, Hammer MF.

Exp Neurol. 2017 Feb;288:134-141. doi: 10.1016/j.expneurol.2016.11.002. Epub 2016 Nov 9.

13.

Differentiated exophytic vulvar intraepithelial lesions are genetically distinct from keratinizing squamous cell carcinomas and contain mutations in PIK3CA.

Watkins JC, Howitt BE, Horowitz NS, Ritterhouse LL, Dong F, MacConaill LE, Garcia E, Lindeman NI, Lee LJ, Berkowitz RS, Nucci MR, Crum CP.

Mod Pathol. 2017 Mar;30(3):448-458. doi: 10.1038/modpathol.2016.187. Epub 2016 Nov 11.

14.

A de novo missense mutation of GABRB2 causes early myoclonic encephalopathy.

Ishii A, Kang JQ, Schornak CC, Hernandez CC, Shen W, Watkins JC, Macdonald RL, Hirose S.

J Med Genet. 2017 Mar;54(3):202-211. doi: 10.1136/jmedgenet-2016-104083. Epub 2016 Oct 27.

15.

Evaluating IPMN and pancreatic carcinoma utilizing quantitative histopathology.

Glazer ES, Zhang HH, Hill KA, Patel C, Kha ST, Yozwiak ML, Bartels H, Nafissi NN, Watkins JC, Alberts DS, Krouse RS.

Cancer Med. 2016 Oct;5(10):2841-2847. doi: 10.1002/cam4.923. Epub 2016 Sep 26.

16.

The Simons Genome Diversity Project: 300 genomes from 142 diverse populations.

Mallick S, Li H, Lipson M, Mathieson I, Gymrek M, Racimo F, Zhao M, Chennagiri N, Nordenfelt S, Tandon A, Skoglund P, Lazaridis I, Sankararaman S, Fu Q, Rohland N, Renaud G, Erlich Y, Willems T, Gallo C, Spence JP, Song YS, Poletti G, Balloux F, van Driem G, de Knijff P, Romero IG, Jha AR, Behar DM, Bravi CM, Capelli C, Hervig T, Moreno-Estrada A, Posukh OL, Balanovska E, Balanovsky O, Karachanak-Yankova S, Sahakyan H, Toncheva D, Yepiskoposyan L, Tyler-Smith C, Xue Y, Abdullah MS, Ruiz-Linares A, Beall CM, Di Rienzo A, Jeong C, Starikovskaya EB, Metspalu E, Parik J, Villems R, Henn BM, Hodoglugil U, Mahley R, Sajantila A, Stamatoyannopoulos G, Wee JT, Khusainova R, Khusnutdinova E, Litvinov S, Ayodo G, Comas D, Hammer MF, Kivisild T, Klitz W, Winkler CA, Labuda D, Bamshad M, Jorde LB, Tishkoff SA, Watkins WS, Metspalu M, Dryomov S, Sukernik R, Singh L, Thangaraj K, Pääbo S, Kelso J, Patterson N, Reich D.

Nature. 2016 Oct 13;538(7624):201-206. doi: 10.1038/nature18964. Epub 2016 Sep 21.

17.

SCN8A-Related Epilepsy with Encephalopathy.

Hammer MF, Wagnon JL, Mefford HC, Meisler MH.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2018.
2016 Aug 25.

18.

Universal Screening for Mismatch-Repair Deficiency in Endometrial Cancers to Identify Patients With Lynch Syndrome and Lynch-like Syndrome.

Watkins JC, Yang EJ, Muto MG, Feltmate CM, Berkowitz RS, Horowitz NS, Syngal S, Yurgelun MB, Chittenden A, Hornick JL, Crum CP, Sholl LM, Howitt BE.

Int J Gynecol Pathol. 2017 Mar;36(2):115-127. doi: 10.1097/PGP.0000000000000312.

PMID:
27556954
19.

Small Traditional Human Communities Sustain Genomic Diversity over Microgeographic Scales despite Linguistic Isolation.

Cox MP, Hudjashov G, Sim A, Savina O, Karafet TM, Sudoyo H, Lansing JS.

Mol Biol Evol. 2016 Sep;33(9):2273-84. doi: 10.1093/molbev/msw099. Epub 2016 Jun 7.

20.

SCN8A encephalopathy: Research progress and prospects.

Meisler MH, Helman G, Hammer MF, Fureman BE, Gaillard WD, Goldin AL, Hirose S, Ishii A, Kroner BL, Lossin C, Mefford HC, Parent JM, Patel M, Schreiber J, Stewart R, Whittemore V, Wilcox K, Wagnon JL, Pearl PL, Vanderver A, Scheffer IE.

Epilepsia. 2016 Jul;57(7):1027-35. doi: 10.1111/epi.13422. Epub 2016 Jun 8.

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