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Items: 1 to 20 of 73

1.

Association of mitochondrial DNA variants with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) symptoms.

Hanson MR, Gu Z, Keinan A, Ye K, Germain A, Billing-Ross P.

J Transl Med. 2016 Dec 20;14(1):342. doi: 10.1186/s12967-016-1104-5.

2.

Association between rs2294020 in X-linked CCDC22 and susceptibility to autoimmune diseases with focus on systemic lupus erythematosus.

D'Amico F, Skarmoutsou E, Lo LJ, Granata M, Trovato C, Rossi GA, Bellocchi C, Marchini M, Scorza R, Mazzarino MC, Keinan A.

Immunol Lett. 2017 Jan;181:58-62. doi: 10.1016/j.imlet.2016.11.011. Epub 2016 Nov 22.

PMID:
27888057
3.

Explosive genetic evidence for explosive human population growth.

Gao F, Keinan A.

Curr Opin Genet Dev. 2016 Dec;41:130-139. doi: 10.1016/j.gde.2016.09.002. Epub 2016 Oct 4. Review.

4.

The genetic history of Cochin Jews from India.

Waldman YY, Biddanda A, Dubrovsky M, Campbell CL, Oddoux C, Friedman E, Atzmon G, Halperin E, Ostrer H, Keinan A.

Hum Genet. 2016 Oct;135(10):1127-43. doi: 10.1007/s00439-016-1698-y. Epub 2016 Jul 4.

5.

Positive Selection on a Regulatory Insertion-Deletion Polymorphism in FADS2 Influences Apparent Endogenous Synthesis of Arachidonic Acid.

Kothapalli KS, Ye K, Gadgil MS, Carlson SE, O'Brien KO, Zhang JY, Park HG, Ojukwu K, Zou J, Hyon SS, Joshi KS, Gu Z, Keinan A, Brenna JT.

Mol Biol Evol. 2016 Jul;33(7):1726-39. doi: 10.1093/molbev/msw049. Epub 2016 Mar 29.

6.

Clustered mutations in hominid genome evolution are consistent with APOBEC3G enzymatic activity.

Pinto Y, Gabay O, Arbiza L, Sams AJ, Keinan A, Levanon EY.

Genome Res. 2016 May;26(5):579-87. doi: 10.1101/gr.199240.115. Epub 2016 Apr 7.

7.

The Genetics of Bene Israel from India Reveals Both Substantial Jewish and Indian Ancestry.

Waldman YY, Biddanda A, Davidson NR, Billing-Ross P, Dubrovsky M, Campbell CL, Oddoux C, Friedman E, Atzmon G, Halperin E, Ostrer H, Keinan A.

PLoS One. 2016 Mar 24;11(3):e0152056. doi: 10.1371/journal.pone.0152056. eCollection 2016.

8.

Mitochondrial DNA variants correlate with symptoms in myalgic encephalomyelitis/chronic fatigue syndrome.

Billing-Ross P, Germain A, Ye K, Keinan A, Gu Z, Hanson MR.

J Transl Med. 2016 Jan 20;14:19. doi: 10.1186/s12967-016-0771-6.

9.

Non-hemorrhagic adrenal infarct in pregnancy - a rare clinical condition diagnosed by non-contrast magnetic resonance image.

Reichman O, Keinan A, Weiss Y, Applbaum Y, Samueloff A.

Eur J Obstet Gynecol Reprod Biol. 2016 Mar;198:173-4. doi: 10.1016/j.ejogrb.2015.12.021. Epub 2015 Dec 31. No abstract available.

PMID:
26777628
10.

Indigenous Arabs are descendants of the earliest split from ancient Eurasian populations.

Rodriguez-Flores JL, Fakhro K, Agosto-Perez F, Ramstetter MD, Arbiza L, Vincent TL, Robay A, Malek JA, Suhre K, Chouchane L, Badii R, Al-Nabet Al-Marri A, Abi Khalil C, Zirie M, Jayyousi A, Salit J, Keinan A, Clark AG, Crystal RG, Mezey JG.

Genome Res. 2016 Feb;26(2):151-62. doi: 10.1101/gr.191478.115. Epub 2016 Jan 4.

11.

Strong Constraint on Human Genes Escaping X-Inactivation Is Modulated by their Expression Level and Breadth in Both Sexes.

Slavney A, Arbiza L, Clark AG, Keinan A.

Mol Biol Evol. 2016 Feb;33(2):384-93. doi: 10.1093/molbev/msv225. Epub 2015 Oct 22.

12.

Inference of Super-exponential Human Population Growth via Efficient Computation of the Site Frequency Spectrum for Generalized Models.

Gao F, Keinan A.

Genetics. 2016 Jan;202(1):235-45. doi: 10.1534/genetics.115.180570. Epub 2015 Oct 8.

13.

A global reference for human genetic variation.

1000 Genomes Project Consortium, Auton A, Brooks LD, Durbin RM, Garrison EP, Kang HM, Korbel JO, Marchini JL, McCarthy S, McVean GA, Abecasis GR.

Nature. 2015 Oct 1;526(7571):68-74. doi: 10.1038/nature15393.

14.

Host genetic variation impacts microbiome composition across human body sites.

Blekhman R, Goodrich JK, Huang K, Sun Q, Bukowski R, Bell JT, Spector TD, Keinan A, Ley RE, Gevers D, Clark AG.

Genome Biol. 2015 Sep 15;16:191. doi: 10.1186/s13059-015-0759-1.

15.

Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases.

Li YR, Li J, Zhao SD, Bradfield JP, Mentch FD, Maggadottir SM, Hou C, Abrams DJ, Chang D, Gao F, Guo Y, Wei Z, Connolly JJ, Cardinale CJ, Bakay M, Glessner JT, Li D, Kao C, Thomas KA, Qiu H, Chiavacci RM, Kim CE, Wang F, Snyder J, Richie MD, Flatø B, Førre Ø, Denson LA, Thompson SD, Becker ML, Guthery SL, Latiano A, Perez E, Resnick E, Russell RK, Wilson DC, Silverberg MS, Annese V, Lie BA, Punaro M, Dubinsky MC, Monos DS, Strisciuglio C, Staiano A, Miele E, Kugathasan S, Ellis JA, Munro JE, Sullivan KE, Wise CA, Chapel H, Cunningham-Rundles C, Grant SF, Orange JS, Sleiman PM, Behrens EM, Griffiths AM, Satsangi J, Finkel TH, Keinan A, Prak ET, Polychronakos C, Baldassano RN, Li H, Keating BJ, Hakonarson H.

Nat Med. 2015 Sep;21(9):1018-27. doi: 10.1038/nm.3933. Epub 2015 Aug 24.

16.

XWAS: A Software Toolset for Genetic Data Analysis and Association Studies of the X Chromosome.

Gao F, Chang D, Biddanda A, Ma L, Guo Y, Zhou Z, Keinan A.

J Hered. 2015 Sep-Oct;106(5):666-71. doi: 10.1093/jhered/esv059. Epub 2015 Aug 12.

17.

X-inactivation informs variance-based testing for X-linked association of a quantitative trait.

Ma L, Hoffman G, Keinan A.

BMC Genomics. 2015 Mar 25;16:241. doi: 10.1186/s12864-015-1463-y.

18.

Population genomic analysis of 962 whole genome sequences of humans reveals natural selection in non-coding regions.

Yu F, Lu J, Liu X, Gazave E, Chang D, Raj S, Hunter-Zinck H, Blekhman R, Arbiza L, Van Hout C, Morrison A, Johnson AD, Bis J, Cupples LA, Psaty BM, Muzny D, Yu J, Gibbs RA, Keinan A, Clark AG, Boerwinkle E.

PLoS One. 2015 Mar 25;10(3):e0121644. doi: 10.1371/journal.pone.0121644. eCollection 2015.

19.

[Laparoscopic adrenalectomy of large adrenal lesions].

Keinan A, Halfteck G, Reissman P.

Harefuah. 2014 Dec;153(12):727-30, 752. Hebrew.

PMID:
25654914
20.

Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel.

Delaneau O, Marchini J; 1000 Genomes Project Consortium; 1000 Genomes Project Consortium.

Nat Commun. 2014 Jun 13;5:3934. doi: 10.1038/ncomms4934.

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