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Items: 1 to 50 of 304

1.

Recontacting or not recontacting? A survey of current practices in clinical genetics centres in Europe.

Sirchia F, Carrieri D, Dheensa S, Benjamin C, Kayserili H, Cordier C, van El CG, Turnpenny PD, Melegh B, Mendes Á, Halbersma-Konings TF, van Langen IM, Lucassen AM, Clarke AJ, Forzano F, Kelly SE.

Eur J Hum Genet. 2018 Apr 23. doi: 10.1038/s41431-018-0131-5. [Epub ahead of print]

PMID:
29681620
2.

Survival in patients with spinocerebellar ataxia types 1, 2, 3, and 6 (EUROSCA): a longitudinal cohort study.

Diallo A, Jacobi H, Cook A, Labrum R, Durr A, Brice A, Charles P, Marelli C, Mariotti C, Nanetti L, Panzeri M, Rakowicz M, Sobanska A, Sulek A, Schmitz-Hübsch T, Schöls L, Hengel H, Melegh B, Filla A, Antenora A, Infante J, Berciano J, van de Warrenburg BP, Timmann D, Boesch S, Pandolfo M, Schulz JB, Bauer P, Giunti P, Kang JS, Klockgether T, Tezenas du Montcel S.

Lancet Neurol. 2018 Apr;17(4):327-334. doi: 10.1016/S1474-4422(18)30042-5. Epub 2018 Mar 13.

PMID:
29553382
3.

Role of carnitine and its derivatives in the development and management of type 2 diabetes.

Bene J, Hadzsiev K, Melegh B.

Nutr Diabetes. 2018 Mar 7;8(1):8. doi: 10.1038/s41387-018-0017-1. Review.

4.

Age-Related Hearing Impairment Associated NAT2, GRM7, GRHL2 Susceptibility Gene Polymorphisms and Haplotypes in Roma and Hungarian Populations.

Matyas P, Postyeni E, Komlosi K, Szalai R, Bene J, Magyari L, Melegh B, Hadzsiev K.

Pathol Oncol Res. 2018 Feb 17. doi: 10.1007/s12253-018-0388-6. [Epub ahead of print]

PMID:
29455378
5.

Correction to: Novel phenotypic variant in the MYH7 spectrum due to a stop-loss mutation in the C-terminal region: a case report.

Bánfai Z, Hadzsiev K, Pál E, Komlósi K, Melegh M, Balikó L, Melegh B.

BMC Med Genet. 2017 Dec 16;18(1):150. doi: 10.1186/s12881-017-0510-8.

6.

Small supernumerary marker chromosome 15 and a ring chromosome 15 associated with a 15q26.3 deletion excluding the IGF1R gene.

Szabó A, Czakó M, Hadzsiev K, Duga B, Bánfai Z, Komlósi K, Melegh B.

Am J Med Genet A. 2018 Feb;176(2):443-449. doi: 10.1002/ajmg.a.38566. Epub 2017 Dec 11.

PMID:
29226546
7.

[Rhabdomyolysis - may it be a metabolic myopathy? Case report and diagnostic algorithm].

Sebők Á, Pál E, Molnár GA, Wittmann I, Berenténé Bene J, Melegh B, Komoly S, Hidvégi T, Balogh L, Szabó A, Zsidegh P.

Orv Hetil. 2017 Nov;158(47):1873-1882. doi: 10.1556/650.2017.30923. Hungarian.

PMID:
29153022
8.

Parallel palaeogenomic transects reveal complex genetic history of early European farmers.

Lipson M, Szécsényi-Nagy A, Mallick S, Pósa A, Stégmár B, Keerl V, Rohland N, Stewardson K, Ferry M, Michel M, Oppenheimer J, Broomandkhoshbacht N, Harney E, Nordenfelt S, Llamas B, Gusztáv Mende B, Köhler K, Oross K, Bondár M, Marton T, Osztás A, Jakucs J, Paluch T, Horváth F, Csengeri P, Koós J, Sebők K, Anders A, Raczky P, Regenye J, Barna JP, Fábián S, Serlegi G, Toldi Z, Gyöngyvér Nagy E, Dani J, Molnár E, Pálfi G, Márk L, Melegh B, Bánfai Z, Domboróczki L, Fernández-Eraso J, Antonio Mujika-Alustiza J, Alonso Fernández C, Jiménez Echevarría J, Bollongino R, Orschiedt J, Schierhold K, Meller H, Cooper A, Burger J, Bánffy E, Alt KW, Lalueza-Fox C, Haak W, Reich D.

Nature. 2017 Nov 16;551(7680):368-372. doi: 10.1038/nature24476. Epub 2017 Nov 8.

PMID:
29144465
9.

CYP2C9 and VKORC1 in therapeutic dosing and safety of acenocoumarol treatment: implication for clinical practice in Hungary.

Varnai R, Sipeky C, Nagy L, Balogh S, Melegh B.

Environ Toxicol Pharmacol. 2017 Dec;56:282-289. doi: 10.1016/j.etap.2017.10.003. Epub 2017 Oct 8.

PMID:
29055218
10.

[Neuroacanthocytosis diagnosis with new generation whole exome sequencing].

Hadzsiev K, Szőts M, Fekete A, Balikó L, Boycott K, Nagy F, Melegh B.

Orv Hetil. 2017 Oct;158(42):1681-1684. doi: 10.1556/650.2017.30880. Hungarian.

PMID:
29037056
11.

Novel phenotypic variant in the MYH7 spectrum due to a stop-loss mutation in the C-terminal region: a case report.

Bánfai Z, Hadzsiev K, Pál E, Komlósi K, Melegh M, Balikó L, Melegh B.

BMC Med Genet. 2017 Sep 19;18(1):105. doi: 10.1186/s12881-017-0463-y. Erratum in: BMC Med Genet. 2017 Dec 16;18(1):150.

12.

Refining the South Asian Origin of the Romani people.

Melegh BI, Banfai Z, Hadzsiev K, Miseta A, Melegh B.

BMC Genet. 2017 Aug 31;18(1):82. doi: 10.1186/s12863-017-0547-x.

13.

[Importance of gross deletions in the diagnosis of tuberous sclerosis complex: the first Hungarian cases].

Kövesdi E, Bene J, Nagy N, Horváth Á, Melegh B, Hadzsiev K.

Orv Hetil. 2017 Jul;158(30):1188-1194. doi: 10.1556/650.2017.30789. Hungarian.

PMID:
28737457
14.

Atypical neurofibromatosis type 1 with unilateral limb hypertrophy mimicking overgrowth syndrome.

Tripolszki K, Farkas K, Sulák A, Szolnoky G, Duga B, Melegh B, Knox RG, Parker VER, Semple RK, Kemény L, Széll M, Nagy N.

Clin Exp Dermatol. 2017 Oct;42(7):763-766. doi: 10.1111/ced.13154. Epub 2017 Jun 8.

PMID:
28598037
15.

Initiating an undiagnosed diseases program in the Western Australian public health system.

Baynam G, Broley S, Bauskis A, Pachter N, McKenzie F, Townshend S, Slee J, Kiraly-Borri C, Vasudevan A, Hawkins A, Schofield L, Helmholz P, Palmer R, Kung S, Walker CE, Molster C, Lewis B, Mina K, Beilby J, Pathak G, Poulton C, Groza T, Zankl A, Roscioli T, Dinger ME, Mattick JS, Gahl W, Groft S, Tifft C, Taruscio D, Lasko P, Kosaki K, Wilhelm H, Melegh B, Carapetis J, Jana S, Chaney G, Johns A, Owen PW, Daly F, Weeramanthri T, Dawkins H, Goldblatt J.

Orphanet J Rare Dis. 2017 May 3;12(1):83. doi: 10.1186/s13023-017-0619-z.

16.

[A8344G mitochondrial DNA mutation observed in two generations].

Fekete A, Hadzsiev K, Bene J, Nászai A, Mátyás P, Till Á, Melegh B.

Orv Hetil. 2017 Mar;158(12):468-471. doi: 10.1556/650.2017.30634. Hungarian.

PMID:
28328248
17.

IL23R single nucleotide polymorphisms could be either beneficial or harmful in ulcerative colitis.

Fischer S, Kövesdi E, Magyari L, Csöngei V, Hadzsiev K, Melegh B, Hegyi P, Sarlós P.

World J Gastroenterol. 2017 Jan 21;23(3):447-454. doi: 10.3748/wjg.v23.i3.447.

18.

Marked Differences of Haplotype Tagging SNP Distribution, Linkage, and Haplotype Profile of APOA5 Gene in Roma Population Samples.

Sumegi K, Duga B, Melegh BI, Banfai Z, Kovesdi E, Maasz A, Melegh B.

Pathol Oncol Res. 2017 Oct;23(4):853-861. doi: 10.1007/s12253-017-0197-3. Epub 2017 Jan 19.

PMID:
28102463
19.

Cytochrome P450 Drug Metabolizing Enzymes in Roma Population Samples: Systematic Review of the Literature.

Szalai R, Hadzsiev K, Melegh B.

Curr Med Chem. 2016;23(31):3632-3652. Review.

PMID:
27516201
20.

[DISEASE BURDEN OP DUCHENNE MUSCULAR DYSTROPHY PATIENTS AND THEIR CAREGIVERS].

Péntek M, Herczegfalvi Á, Molnár MJ, Szőnyi LP, Kosztolányi G, Pfliegler G, Melegh B, Boncz I, Brodszky V, Baji P, Szegedi M, Pogány G, Gulácsi L.

Ideggyogy Sz. 2016 Mar 30;69(5-6):183-93. Hungarian.

PMID:
27468608
21.

On the distribution of intranuclear and cytoplasmic aggregates in the brainstem of patients with spinocerebellar ataxia type 2 and 3.

Seidel K, Siswanto S, Fredrich M, Bouzrou M, den Dunnen WFA, Özerden I, Korf HW, Melegh B, de Vries JJ, Brunt ER, Auburger G, Rüb U.

Brain Pathol. 2017 May;27(3):345-355. doi: 10.1111/bpa.12412. Epub 2016 Aug 2.

PMID:
27377427
22.

Evidence for Genetic Overlap Between Schizophrenia and Age at First Birth in Women.

Mehta D, Tropf FC, Gratten J, Bakshi A, Zhu Z, Bacanu SA, Hemani G, Magnusson PK, Barban N, Esko T, Metspalu A, Snieder H, Mowry BJ, Kendler KS, Yang J, Visscher PM, McGrath JJ, Mills MC, Wray NR, Lee SH; Schizophrenia Working Group of the Psychiatric Genomics Consortium, LifeLines Cohort Study, and TwinsUK, Andreassen OA, Bramon E, Bruggeman R, Buxbaum JD, Cairns MJ, Cantor RM, Cloninger CR, Cohen D, Crespo-Facorro B, Darvasi A, DeLisi LE, Dinan T, Djurovic S, Donohoe G, Drapeau E, Escott-Price V, Freimer NB, Georgieva L, de Haan L, Henskens FA, Joa I, Julià A, Khrunin A, Lerer B, Limborska S, Loughland CM, Macek M Jr, Magnusson PK, Marsal S, McCarley RW, McIntosh AM, McQuillin A, Melegh B, Michie PT, Morris DW, Murphy KC, Myin-Germeys I, Olincy A, Van Os J, Pantelis C, Posthuma D, Quested D, Schall U, Scott RJ, Seidman LJ, Toncheva D, Tooney PA, Waddington J, Weinberger DR, Weiser M, Wu JQ.

JAMA Psychiatry. 2016 May 1;73(5):497-505. doi: 10.1001/jamapsychiatry.2016.0129.

23.

Kleefstra syndrome in Hungarian patients: additional symptoms besides the classic phenotype.

Hadzsiev K, Komlosi K, Czako M, Duga B, Szalai R, Szabo A, Postyeni E, Szabo T, Kosztolanyi G, Melegh B.

Mol Cytogenet. 2016 Feb 25;9:22. doi: 10.1186/s13039-016-0231-2. eCollection 2016.

24.

[De novo SCN1A gene deletion in therapy-resistant Dravet syndrome].

Bene J, Hadzsiev K, Komlósi K, Kövesdi E, Mátyás P, Melegh B.

Orv Hetil. 2015 Dec 6;156(49):2009-12. doi: 10.1556/650.2015.30308. Hungarian.

PMID:
26614543
25.

Undiagnosed Diseases Network International (UDNI): White paper for global actions to meet patient needs.

Taruscio D, Groft SC, Cederroth H, Melegh B, Lasko P, Kosaki K, Baynam G, McCray A, Gahl WA.

Mol Genet Metab. 2015 Dec;116(4):223-5. doi: 10.1016/j.ymgme.2015.11.003. Epub 2015 Nov 5.

PMID:
26596705
26.

Genome Sequences of Three Turkey Orthoreovirus Strains Isolated in Hungary.

Dandár E, Fehér E, Bálint Á, Kisfali P, Melegh B, Mató T, Kecskeméti S, Palya V, Bányai K, Farkas SL.

Genome Announc. 2015 Nov 19;3(6). pii: e01333-15. doi: 10.1128/genomeA.01333-15.

27.

[Catch-22? Wide variety of phenotypes associated with the chromosome 22q11 deletion syndrome in two patients].

Till Á, Hadzsiev K, Lőcsei-Fekete A, Czakó M, Duga B, Melegh B.

Orv Hetil. 2015 Nov 8;156(45):1834-8. doi: 10.1556/650.2015.30283. Hungarian.

PMID:
26522857
28.

Interethnic differences of cytochrome P450 gene polymorphisms may influence outcome of taxane therapy in Roma and Hungarian populations.

Szalai R, Ganczer A, Magyari L, Matyas P, Bene J, Melegh B.

Drug Metab Pharmacokinet. 2015 Dec;30(6):453-6. doi: 10.1016/j.dmpk.2015.08.001. Epub 2015 Aug 10.

PMID:
26507668
29.

Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study.

Jacobi H, du Montcel ST, Bauer P, Giunti P, Cook A, Labrum R, Parkinson MH, Durr A, Brice A, Charles P, Marelli C, Mariotti C, Nanetti L, Panzeri M, Rakowicz M, Sulek A, Sobanska A, Schmitz-Hübsch T, Schöls L, Hengel H, Baliko L, Melegh B, Filla A, Antenora A, Infante J, Berciano J, van de Warrenburg BP, Timmann D, Szymanski S, Boesch S, Kang JS, Pandolfo M, Schulz JB, Molho S, Diallo A, Klockgether T.

Lancet Neurol. 2015 Nov;14(11):1101-8. doi: 10.1016/S1474-4422(15)00202-1. Epub 2015 Sep 13.

PMID:
26377379
30.

Marked differences in frequencies of statin therapy relevant SLCO1B1 variants and haplotypes between Roma and Hungarian populations.

Nagy A, Sipeky C, Szalai R, Melegh BI, Matyas P, Ganczer A, Toth K, Melegh B.

BMC Genet. 2015 Sep 3;16:108. doi: 10.1186/s12863-015-0262-4.

31.

Interethnic variability of CYP4F2 (V433M) in admixed population of Roma and Hungarians.

Sipeky C, Weber A, Melegh BI, Matyas P, Janicsek I, Szalai R, Szabo I, Varnai R, Tarlos G, Ganczer A, Melegh B.

Environ Toxicol Pharmacol. 2015 Jul;40(1):280-3. doi: 10.1016/j.etap.2015.05.008. Epub 2015 May 22.

PMID:
26176903
32.

Partial tetrasomy of the proximal long arm of chromosome 15 in two patients: the significance of the gene dosage in terms of phenotype.

Szabo A, Czako M, Hadzsiev K, Duga B, Komlosi K, Melegh B.

Mol Cytogenet. 2015 Jun 25;8:41. doi: 10.1186/s13039-015-0137-4. eCollection 2015.

33.

Identification of SLC22A5 Gene Mutation in a Family with Carnitine Uptake Defect.

Mutlu-Albayrak H, Bene J, Oflaz MB, Tanyalçın T, Çaksen H, Melegh B.

Case Rep Genet. 2015;2015:259627. doi: 10.1155/2015/259627. Epub 2015 May 5.

34.

Towards a European consensus for reporting incidental findings during clinical NGS testing.

Hehir-Kwa JY, Claustres M, Hastings RJ, van Ravenswaaij-Arts C, Christenhusz G, Genuardi M, Melegh B, Cambon-Thomsen A, Patsalis P, Vermeesch J, Cornel MC, Searle B, Palotie A, Capoluongo E, Peterlin B, Estivill X, Robinson PN.

Eur J Hum Genet. 2015 Dec;23(12):1601-6. doi: 10.1038/ejhg.2015.111. Epub 2015 Jun 3.

35.

Extreme differences in SLCO1B3 functional polymorphisms in Roma and Hungarian populations.

Nagy A, Szalai R, Magyari L, Bene J, Toth K, Melegh B.

Environ Toxicol Pharmacol. 2015 May;39(3):1246-51. doi: 10.1016/j.etap.2015.04.019. Epub 2015 May 8.

PMID:
26005078
36.

Increased prevalence of functional minor allele variants of drug metabolizing CYP2B6 and CYP2D6 genes in Roma population samples.

Weber A, Szalai R, Sipeky C, Magyari L, Melegh M, Jaromi L, Matyas P, Duga B, Kovesdi E, Hadzsiev K, Melegh B.

Pharmacol Rep. 2015 Jun;67(3):460-4. doi: 10.1016/j.pharep.2014.11.006. Epub 2014 Nov 27.

PMID:
25933954
37.

MARVELD2 (DFNB49) mutations in the hearing impaired Central European Roma population--prevalence, clinical impact and the common origin.

Mašindová I, Šoltýsová A, Varga L, Mátyás P, Ficek A, Hučková M, Sůrová M, Šafka-Brožková D, Anwar S, Bene J, Straka S, Janicsek I, Ahmed ZM, Seeman P, Melegh B, Profant M, Klimeš I, Riazuddin S, Kádasi Ľ, Gašperíková D.

PLoS One. 2015 Apr 17;10(4):e0124232. doi: 10.1371/journal.pone.0124232. eCollection 2015.

38.

Epilepsy in Rett syndrome--lessons from the Rett networked database.

Nissenkorn A, Levy-Drummer RS, Bondi O, Renieri A, Villard L, Mari F, Mencarelli MA, Lo Rizzo C, Meloni I, Pineda M, Armstrong J, Clarke A, Bahi-Buisson N, Mejaski BV, Djuric M, Craiu D, Djukic A, Pini G, Bisgaard AM, Melegh B, Vignoli A, Russo S, Anghelescu C, Veneselli E, Hayek J, Ben-Zeev B.

Epilepsia. 2015 Apr;56(4):569-76. doi: 10.1111/epi.12941. Epub 2015 Mar 19.

39.

Phenotypic variability in a Hungarian patient with the 4q21 microdeletion syndrome.

Komlósi K, Duga B, Hadzsiev K, Czakó M, Kosztolányi G, Fogarasi A, Melegh B.

Mol Cytogenet. 2015 Mar 3;8:16. doi: 10.1186/s13039-015-0118-7. eCollection 2015.

40.

[Genetic testing in hereditary spastic paraplegia].

Hadzsiev K, Balikó L, Komlósi K, Lőcsei-Fekete A, Csábi G, Bene J, Kisfali P, Melegh B.

Orv Hetil. 2015 Jan 18;156(3):113-7. doi: 10.1556/OH.2015.30014. Hungarian.

PMID:
25577683
41.

Functional variants of lipid level modifier MLXIPL, GCKR, GALNT2, CILP2, ANGPTL3 and TRIB1 genes in healthy Roma and Hungarian populations.

Sumegi K, Jaromi L, Magyari L, Kovesdi E, Duga B, Szalai R, Maasz A, Matyas P, Janicsek I, Melegh B.

Pathol Oncol Res. 2015 Jul;21(3):743-9. doi: 10.1007/s12253-014-9884-5. Epub 2015 Jan 9.

PMID:
25573592
42.

Partial trisomy of the pericentromeric region of chromosome 5 in a girl with binder phenotype.

Hadzsiev K, Dávid D, Szabó G, Czakó M, Melegh B, Kosztolányi G.

Cytogenet Genome Res. 2014;144(3):190-5. doi: 10.1159/000369653. Epub 2014 Dec 20.

PMID:
25531548
43.

Genetic polymorphisms in promoter and intronic regions of CYP1A2 gene in Roma and Hungarian population samples.

Szalai R, Magyari L, Matyas P, Duga B, Banfai Z, Szabo A, Kovesdi E, Melegh B.

Environ Toxicol Pharmacol. 2014 Nov;38(3):814-20. doi: 10.1016/j.etap.2014.09.012. Epub 2014 Sep 28.

PMID:
25461540
44.

Erratum to: Significant interethnic differences in functional variants of PON1 and P2RY12 genes in Roma and Hungarian population samples.

Janicsek I, Sipeky C, Bene J, Duga B, Melegh BI, Sümegi K, Jaromi L, Magyari L, Melegh B.

Mol Biol Rep. 2015 Jan;42(1):317. doi: 10.1007/s11033-014-3798-x. No abstract available.

PMID:
25366175
45.

[Cystic fibrosis -- disease burden and health-related quality of life of patients and their caregivers: results of the European BURQOL-RD survey in Hungary].

Péntek M, Kosztolányi G, Melegh B, Halász A, Pogány G, Baji P, Brodszky V, Vártokné Hevér N, Boncz I, Gulácsi L.

Orv Hetil. 2014 Oct 19;155(42):1673-84. doi: 10.1556/OH.2014.30016. Hungarian.

PMID:
25305725
46.

Significant interethnic differencies in functional variants of PON1 and P2RY12 genes in Roma and Hungarian population samples.

Janicsek I, Sipeky C, Bene J, Duga B, Melegh BI, Sümegi K, Jaromi L, Magyari L, Melegh B.

Mol Biol Rep. 2015 Jan;42(1):227-32. doi: 10.1007/s11033-014-3762-9. Epub 2014 Oct 9. Erratum in: Mol Biol Rep. 2015 Jan;42(1):317. Melegh, Bela [corrected to Melegh, Bela I].

PMID:
25297118
47.

[Attention deficit hyperactivity disorder analyzed with array comparative genome hybridization method. Case report].

Duga B, Czakó M, Komlósi K, Hadzsiev K, Sümegi K, Kisfali P, Melegh M, Melegh B.

Orv Hetil. 2014 Oct 5;155(40):1598-601. doi: 10.1556/OH.2014.30006. Hungarian.

PMID:
25261991
48.

Large-scale whole genome sequencing identifies country-wide spread of an emerging G9P[8] rotavirus strain in Hungary, 2012.

Dóró R, Mihalov-Kovács E, Marton S, László B, Deák J, Jakab F, Juhász Á, Kisfali P, Martella V, Melegh B, Molnár P, Sántha I, Schneider F, Bányai K.

Infect Genet Evol. 2014 Dec;28:495-512. doi: 10.1016/j.meegid.2014.09.016. Epub 2014 Sep 17.

PMID:
25239526
49.

Interleukins and interleukin receptors in rheumatoid arthritis: Research, diagnostics and clinical implications.

Magyari L, Varszegi D, Kovesdi E, Sarlos P, Farago B, Javorhazy A, Sumegi K, Banfai Z, Melegh B.

World J Orthop. 2014 Sep 18;5(4):516-36. doi: 10.5312/wjo.v5.i4.516. eCollection 2014 Sep 18. Review.

50.

Ancient human genomes suggest three ancestral populations for present-day Europeans.

Lazaridis I, Patterson N, Mittnik A, Renaud G, Mallick S, Kirsanow K, Sudmant PH, Schraiber JG, Castellano S, Lipson M, Berger B, Economou C, Bollongino R, Fu Q, Bos KI, Nordenfelt S, Li H, de Filippo C, Prüfer K, Sawyer S, Posth C, Haak W, Hallgren F, Fornander E, Rohland N, Delsate D, Francken M, Guinet JM, Wahl J, Ayodo G, Babiker HA, Bailliet G, Balanovska E, Balanovsky O, Barrantes R, Bedoya G, Ben-Ami H, Bene J, Berrada F, Bravi CM, Brisighelli F, Busby GB, Cali F, Churnosov M, Cole DE, Corach D, Damba L, van Driem G, Dryomov S, Dugoujon JM, Fedorova SA, Gallego Romero I, Gubina M, Hammer M, Henn BM, Hervig T, Hodoglugil U, Jha AR, Karachanak-Yankova S, Khusainova R, Khusnutdinova E, Kittles R, Kivisild T, Klitz W, Kučinskas V, Kushniarevich A, Laredj L, Litvinov S, Loukidis T, Mahley RW, Melegh B, Metspalu E, Molina J, Mountain J, Näkkäläjärvi K, Nesheva D, Nyambo T, Osipova L, Parik J, Platonov F, Posukh O, Romano V, Rothhammer F, Rudan I, Ruizbakiev R, Sahakyan H, Sajantila A, Salas A, Starikovskaya EB, Tarekegn A, Toncheva D, Turdikulova S, Uktveryte I, Utevska O, Vasquez R, Villena M, Voevoda M, Winkler CA, Yepiskoposyan L, Zalloua P, Zemunik T, Cooper A, Capelli C, Thomas MG, Ruiz-Linares A, Tishkoff SA, Singh L, Thangaraj K, Villems R, Comas D, Sukernik R, Metspalu M, Meyer M, Eichler EE, Burger J, Slatkin M, Pääbo S, Kelso J, Reich D, Krause J.

Nature. 2014 Sep 18;513(7518):409-13. doi: 10.1038/nature13673.

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