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Items: 1 to 50 of 174

1.

Inferring Transmission Histories of Rare Alleles in Population-Scale Genealogies.

Nelson D, Moreau C, de Vriendt M, Zeng Y, Preuss C, Vézina H, Milot E, Andelfinger G, Labuda D, Gravel S.

Am J Hum Genet. 2018 Dec 6;103(6):893-906. doi: 10.1016/j.ajhg.2018.10.017.

PMID:
30526866
2.

The genomic history of southeastern Europe.

Mathieson I, Alpaslan-Roodenberg S, Posth C, Szécsényi-Nagy A, Rohland N, Mallick S, Olalde I, Broomandkhoshbacht N, Candilio F, Cheronet O, Fernandes D, Ferry M, Gamarra B, Fortes GG, Haak W, Harney E, Jones E, Keating D, Krause-Kyora B, Kucukkalipci I, Michel M, Mittnik A, Nägele K, Novak M, Oppenheimer J, Patterson N, Pfrengle S, Sirak K, Stewardson K, Vai S, Alexandrov S, Alt KW, Andreescu R, Antonović D, Ash A, Atanassova N, Bacvarov K, Gusztáv MB, Bocherens H, Bolus M, Boroneanţ A, Boyadzhiev Y, Budnik A, Burmaz J, Chohadzhiev S, Conard NJ, Cottiaux R, Čuka M, Cupillard C, Drucker DG, Elenski N, Francken M, Galabova B, Ganetsovski G, Gély B, Hajdu T, Handzhyiska V, Harvati K, Higham T, Iliev S, Janković I, Karavanić I, Kennett DJ, Komšo D, Kozak A, Labuda D, Lari M, Lazar C, Leppek M, Leshtakov K, Vetro DL, Los D, Lozanov I, Malina M, Martini F, McSweeney K, Meller H, Menđušić M, Mirea P, Moiseyev V, Petrova V, Price TD, Simalcsik A, Sineo L, Šlaus M, Slavchev V, Stanev P, Starović A, Szeniczey T, Talamo S, Teschler-Nicola M, Thevenet C, Valchev I, Valentin F, Vasilyev S, Veljanovska F, Venelinova S, Veselovskaya E, Viola B, Virag C, Zaninović J, Zäuner S, Stockhammer PW, Catalano G, Krauß R, Caramelli D, Zariņa G, Gaydarska B, Lillie M, Nikitin AG, Potekhina I, Papathanasiou A, Borić D, Bonsall C, Krause J, Pinhasi R, Reich D.

Nature. 2018 Mar 8;555(7695):197-203. doi: 10.1038/nature25778. Epub 2018 Feb 21.

3.

Genome diversity in the Neolithic Globular Amphorae culture and the spread of Indo-European languages.

Tassi F, Vai S, Ghirotto S, Lari M, Modi A, Pilli E, Brunelli A, Susca RR, Budnik A, Labuda D, Alberti F, Lalueza-Fox C, Reich D, Caramelli D, Barbujani G.

Proc Biol Sci. 2017 Nov 29;284(1867). pii: 20171540. doi: 10.1098/rspb.2017.1540.

4.

Mother's curse neutralizes natural selection against a human genetic disease over three centuries.

Milot E, Moreau C, Gagnon A, Cohen AA, Brais B, Labuda D.

Nat Ecol Evol. 2017 Sep;1(9):1400-1406. doi: 10.1038/s41559-017-0276-6. Epub 2017 Aug 21.

PMID:
29046555
5.

Genetic Structure of First Nation Communities in the Pacific Northwest.

Hughes CE, Rogers MP, Owings AC, Petzelt B, Mitchell J, Harry H, Williams T, Goldberg D, Labuda D, Smith DG, Cybulski JS, Malhi RS.

Hum Biol. 2016 Oct;88(4):251-263.

PMID:
28826319
6.

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.

7.

Joubert Syndrome in French Canadians and Identification of Mutations in CEP104.

Srour M, Hamdan FF, McKnight D, Davis E, Mandel H, Schwartzentruber J, Martin B, Patry L, Nassif C, Dionne-Laporte A, Ospina LH, Lemyre E, Massicotte C, Laframboise R, Maranda B, Labuda D, Décarie JC, Rypens F, Goldsher D, Fallet-Bianco C, Soucy JF, Laberge AM, Maftei C; Care4Rare Canada Consortium, Boycott K, Brais B, Boucher RM, Rouleau GA, Katsanis N, Majewski J, Elpeleg O, Kukolich MK, Shalev S, Michaud JL.

Am J Hum Genet. 2015 Nov 5;97(5):744-53. doi: 10.1016/j.ajhg.2015.09.009. Epub 2015 Oct 17.

8.

Global diversity, population stratification, and selection of human copy-number variation.

Sudmant PH, Mallick S, Nelson BJ, Hormozdiari F, Krumm N, Huddleston J, Coe BP, Baker C, Nordenfelt S, Bamshad M, Jorde LB, Posukh OL, Sahakyan H, Watkins WS, Yepiskoposyan L, Abdullah MS, Bravi CM, Capelli C, Hervig T, Wee JT, Tyler-Smith C, van Driem G, Romero IG, Jha AR, Karachanak-Yankova S, Toncheva D, Comas D, Henn B, Kivisild T, Ruiz-Linares A, Sajantila A, Metspalu E, Parik J, Villems R, Starikovskaya EB, Ayodo G, Beall CM, Di Rienzo A, Hammer MF, Khusainova R, Khusnutdinova E, Klitz W, Winkler C, Labuda D, Metspalu M, Tishkoff SA, Dryomov S, Sukernik R, Patterson N, Reich D, Eichler EE.

Science. 2015 Sep 11;349(6253):aab3761. doi: 10.1126/science.aab3761. Epub 2015 Aug 6.

9.

GENLIB: an R package for the analysis of genealogical data.

Gauvin H, Lefebvre JF, Moreau C, Lavoie EM, Labuda D, Vézina H, Roy-Gagnon MH.

BMC Bioinformatics. 2015 May 15;16:160. doi: 10.1186/s12859-015-0581-5.

10.

A homozygous mutation in SLC1A4 in siblings with severe intellectual disability and microcephaly.

Srour M, Hamdan FF, Gan-Or Z, Labuda D, Nassif C, Oskoui M, Gana-Weisz M, Orr-Urtreger A, Rouleau GA, Michaud JL.

Clin Genet. 2015 Jul;88(1):e1-4. doi: 10.1111/cge.12605. Epub 2015 May 28.

PMID:
25930971
11.

Disruption of CLPB is associated with congenital microcephaly, severe encephalopathy and 3-methylglutaconic aciduria.

Capo-Chichi JM, Boissel S, Brustein E, Pickles S, Fallet-Bianco C, Nassif C, Patry L, Dobrzeniecka S, Liao M, Labuda D, Samuels ME, Hamdan FF, Vande Velde C, Rouleau GA, Drapeau P, Michaud JL.

J Med Genet. 2015 May;52(5):303-11. doi: 10.1136/jmedgenet-2014-102952. Epub 2015 Feb 3.

PMID:
25650066
12.

Nonsense mutations in BAG3 are associated with early-onset dilated cardiomyopathy in French Canadians.

Chami N, Tadros R, Lemarbre F, Lo KS, Beaudoin M, Robb L, Labuda D, Tardif JC, Racine N, Talajic M, Lettre G.

Can J Cardiol. 2014 Dec;30(12):1655-61. doi: 10.1016/j.cjca.2014.09.030. Epub 2014 Oct 2.

PMID:
25448463
13.

Mutations in SGOL1 cause a novel cohesinopathy affecting heart and gut rhythm.

Chetaille P, Preuss C, Burkhard S, Côté JM, Houde C, Castilloux J, Piché J, Gosset N, Leclerc S, Wünnemann F, Thibeault M, Gagnon C, Galli A, Tuck E, Hickson GR, El Amine N, Boufaied I, Lemyre E, de Santa Barbara P, Faure S, Jonzon A, Cameron M, Dietz HC, Gallo-McFarlane E, Benson DW, Moreau C, Labuda D; FORGE Canada Consortium, Zhan SH, Shen Y, Jomphe M, Jones SJ, Bakkers J, Andelfinger G.

Nat Genet. 2014 Nov;46(11):1245-9. doi: 10.1038/ng.3113. Epub 2014 Oct 5.

PMID:
25282101
14.

The catalytic function of hormone-sensitive lipase is essential for fertility in male mice.

Wang SP, Wu JW, Bourdages H, Lefebvre JF, Casavant S, Leavitt BR, Labuda D, Trasler J, Smith CE, Hermo L, Mitchell GA.

Endocrinology. 2014 Aug;155(8):3047-53. doi: 10.1210/en.2014-1031. Epub 2014 May 5.

PMID:
24797631
15.

X-linked MTMR8 diversity and evolutionary history of sub-Saharan populations.

Labuda D, Yotova V, Lefebvre JF, Moreau C, Utermann G, Williams SM.

PLoS One. 2013 Nov 25;8(11):e80710. doi: 10.1371/journal.pone.0080710. eCollection 2013.

16.

Genome-wide patterns of identity-by-descent sharing in the French Canadian founder population.

Gauvin H, Moreau C, Lefebvre JF, Laprise C, Vézina H, Labuda D, Roy-Gagnon MH.

Eur J Hum Genet. 2014 Jun;22(6):814-21. doi: 10.1038/ejhg.2013.227. Epub 2013 Oct 16.

17.

Reconciling migration models to the Americas with the variation of North American native mitogenomes.

Achilli A, Perego UA, Lancioni H, Olivieri A, Gandini F, Hooshiar Kashani B, Battaglia V, Grugni V, Angerhofer N, Rogers MP, Herrera RJ, Woodward SR, Labuda D, Smith DG, Cybulski JS, Semino O, Malhi RS, Torroni A.

Proc Natl Acad Sci U S A. 2013 Aug 27;110(35):14308-13. doi: 10.1073/pnas.1306290110. Epub 2013 Aug 12.

18.

Native American admixture in the Quebec founder population.

Moreau C, Lefebvre JF, Jomphe M, Bhérer C, Ruiz-Linares A, Vézina H, Roy-Gagnon MH, Labuda D.

PLoS One. 2013 Jun 12;8(6):e65507. doi: 10.1371/journal.pone.0065507. Print 2013.

19.

Mutations in TMEM231 cause Joubert syndrome in French Canadians.

Srour M, Hamdan FF, Schwartzentruber JA, Patry L, Ospina LH, Shevell MI, Désilets V, Dobrzeniecka S, Mathonnet G, Lemyre E, Massicotte C, Labuda D, Amrom D, Andermann E, Sébire G, Maranda B; FORGE Canada Consortium, Rouleau GA, Majewski J, Michaud JL.

J Med Genet. 2012 Oct;49(10):636-41. doi: 10.1136/jmedgenet-2012-101132. Epub 2012 Sep 25.

PMID:
23012439
20.

Reconstructing Native American population history.

Reich D, Patterson N, Campbell D, Tandon A, Mazieres S, Ray N, Parra MV, Rojas W, Duque C, Mesa N, García LF, Triana O, Blair S, Maestre A, Dib JC, Bravi CM, Bailliet G, Corach D, Hünemeier T, Bortolini MC, Salzano FM, Petzl-Erler ML, Acuña-Alonzo V, Aguilar-Salinas C, Canizales-Quinteros S, Tusié-Luna T, Riba L, Rodríguez-Cruz M, Lopez-Alarcón M, Coral-Vazquez R, Canto-Cetina T, Silva-Zolezzi I, Fernandez-Lopez JC, Contreras AV, Jimenez-Sanchez G, Gómez-Vázquez MJ, Molina J, Carracedo A, Salas A, Gallo C, Poletti G, Witonsky DB, Alkorta-Aranburu G, Sukernik RI, Osipova L, Fedorova SA, Vasquez R, Villena M, Moreau C, Barrantes R, Pauls D, Excoffier L, Bedoya G, Rothhammer F, Dugoujon JM, Larrouy G, Klitz W, Labuda D, Kidd J, Kidd K, Di Rienzo A, Freimer NB, Price AL, Ruiz-Linares A.

Nature. 2012 Aug 16;488(7411):370-4. doi: 10.1038/nature11258. Erratum in: Nature. 2012 Nov 8;491(7423):288.

21.

Genotype-based test in mapping cis-regulatory variants from allele-specific expression data.

Lefebvre JF, Vello E, Ge B, Montgomery SB, Dermitzakis ET, Pastinen T, Labuda D.

PLoS One. 2012;7(6):e38667. doi: 10.1371/journal.pone.0038667. Epub 2012 Jun 7.

22.

Mutations in C5ORF42 cause Joubert syndrome in the French Canadian population.

Srour M, Schwartzentruber J, Hamdan FF, Ospina LH, Patry L, Labuda D, Massicotte C, Dobrzeniecka S, Capo-Chichi JM, Papillon-Cavanagh S, Samuels ME, Boycott KM, Shevell MI, Laframboise R, Désilets V; FORGE Canada Consortium, Maranda B, Rouleau GA, Majewski J, Michaud JL.

Am J Hum Genet. 2012 Apr 6;90(4):693-700. doi: 10.1016/j.ajhg.2012.02.011. Epub 2012 Mar 15.

23.

Deep human genealogies reveal a selective advantage to be on an expanding wave front.

Moreau C, Bhérer C, Vézina H, Jomphe M, Labuda D, Excoffier L.

Science. 2011 Nov 25;334(6059):1148-50. doi: 10.1126/science.1212880. Epub 2011 Nov 3.

24.

Admixed ancestry and stratification of Quebec regional populations.

Bherer C, Labuda D, Roy-Gagnon MH, Houde L, Tremblay M, Vézina H.

Am J Phys Anthropol. 2011 Mar;144(3):432-41. doi: 10.1002/ajpa.21424. Epub 2010 Nov 10.

PMID:
21302269
25.

An X-linked haplotype of Neandertal origin is present among all non-African populations.

Yotova V, Lefebvre JF, Moreau C, Gbeha E, Hovhannesyan K, Bourgeois S, Bédarida S, Azevedo L, Amorim A, Sarkisian T, Avogbe PH, Chabi N, Dicko MH, Kou' Santa Amouzou ES, Sanni A, Roberts-Thomson J, Boettcher B, Scott RJ, Labuda D.

Mol Biol Evol. 2011 Jul;28(7):1957-62. doi: 10.1093/molbev/msr024. Epub 2011 Jan 25.

PMID:
21266489
26.

Genomic and genealogical investigation of the French Canadian founder population structure.

Roy-Gagnon MH, Moreau C, Bherer C, St-Onge P, Sinnett D, Laprise C, Vézina H, Labuda D.

Hum Genet. 2011 May;129(5):521-31. doi: 10.1007/s00439-010-0945-x. Epub 2011 Jan 15.

PMID:
21234765
27.

When genetics and genealogies tell different stories-maternal lineages in Gaspesia.

Moreau C, Vézina H, Jomphe M, Lavoie EM, Roy-Gagnon MH, Labuda D.

Ann Hum Genet. 2011 Mar;75(2):247-54. doi: 10.1111/j.1469-1809.2010.00617.x. Epub 2010 Nov 8.

28.

Contrasting patterns of nuclear and mtDNA diversity in Native American populations.

Yang NN, Mazières S, Bravi C, Ray N, Wang S, Burley MW, Bedoya G, Rojas W, Parra MV, Molina JA, Gallo C, Poletti G, Hill K, Hurtado AM, Petzl-Erler ML, Tsuneto LT, Klitz W, Barrantes R, Llop E, Rothhammer F, Labuda D, Salzano FM, Bortolini MC, Excoffier L, Dugoujon JM, Ruiz-Linares A.

Ann Hum Genet. 2010 Nov;74(6):525-38. doi: 10.1111/j.1469-1809.2010.00608.x. Epub 2010 Sep 30.

29.

Mutability of Y-chromosomal microsatellites: rates, characteristics, molecular bases, and forensic implications.

Ballantyne KN, Goedbloed M, Fang R, Schaap O, Lao O, Wollstein A, Choi Y, van Duijn K, Vermeulen M, Brauer S, Decorte R, Poetsch M, von Wurmb-Schwark N, de Knijff P, Labuda D, Vézina H, Knoblauch H, Lessig R, Roewer L, Ploski R, Dobosz T, Henke L, Henke J, Furtado MR, Kayser M.

Am J Hum Genet. 2010 Sep 10;87(3):341-53. doi: 10.1016/j.ajhg.2010.08.006.

30.

Female-to-male breeding ratio in modern humans-an analysis based on historical recombinations.

Labuda D, Lefebvre JF, Nadeau P, Roy-Gagnon MH.

Am J Hum Genet. 2010 Mar 12;86(3):353-63. doi: 10.1016/j.ajhg.2010.01.029. Epub 2010 Feb 25. Erratum in: Am J Hum Genet. 2010 Jun 11;86(6):982.

31.

Haplotype allelic classes for detecting ongoing positive selection.

Hussin J, Nadeau P, Lefebvre JF, Labuda D.

BMC Bioinformatics. 2010 Jan 28;11:65. doi: 10.1186/1471-2105-11-65.

32.

Brief communication: patterns of linkage disequilibrium and haplotype diversity at Xq13 in six Native American populations.

Wang S, Bedoya G, Labuda D, Ruiz-Linares A.

Am J Phys Anthropol. 2010 Jul;142(3):476-80. doi: 10.1002/ajpa.21234.

PMID:
20034009
33.

Functional impact of sequence variation in the promoter region of TGFB1.

Healy J, Dionne J, Bélanger H, Larivière M, Beaulieu P, Labuda D, Sinnett D.

Int J Cancer. 2009 Sep 15;125(6):1483-9. doi: 10.1002/ijc.24526.

34.

X-chromosome lineages and the settlement of the Americas.

Bourgeois S, Yotova V, Wang S, Bourtoumieu S, Moreau C, Michalski R, Moisan JP, Hill K, Hurtado AM, Ruiz-Linares A, Labuda D.

Am J Phys Anthropol. 2009 Nov;140(3):417-28. doi: 10.1002/ajpa.21084.

PMID:
19425105
35.

Genetic heterogeneity in regional populations of Quebec--parental lineages in the Gaspe Peninsula.

Moreau C, Vézina H, Yotova V, Hamon R, de Knijff P, Sinnett D, Labuda D.

Am J Phys Anthropol. 2009 Aug;139(4):512-22. doi: 10.1002/ajpa.21012.

PMID:
19226649
36.

Ethnic differences in the frequency of the cardioprotective C679X PCSK9 mutation in a West African population.

Sirois F, Gbeha E, Sanni A, Chretien M, Labuda D, Mbikay M.

Genet Test. 2008 Sep;12(3):377-80. doi: 10.1089/gte.2008.0013.

PMID:
18652535
37.

Genetic diversity patterns at the human clock gene period 2 are suggestive of population-specific positive selection.

Cruciani F, Trombetta B, Labuda D, Modiano D, Torroni A, Costa R, Scozzari R.

Eur J Hum Genet. 2008 Dec;16(12):1526-34. doi: 10.1038/ejhg.2008.105. Epub 2008 Jun 25.

38.

Fraction of informative recombinations: a heuristic approach to analyze recombination rates.

Lefebvre JF, Labuda D.

Genetics. 2008 Apr;178(4):2069-79. doi: 10.1534/genetics.107.082255.

39.

Genetic variation in the enigmatic Altaian Kazakhs of South-Central Russia: insights into Turkic population history.

Gokcumen O, Dulik MC, Pai AA, Zhadanov SI, Rubinstein S, Osipova LP, Andreenkov OV, Tabikhanova LE, Gubina MA, Labuda D, Schurr TG.

Am J Phys Anthropol. 2008 Jul;136(3):278-93. doi: 10.1002/ajpa.20802.

PMID:
18322915
40.

DNA variants in the dihydrofolate reductase gene and outcome in childhood ALL.

Dulucq S, St-Onge G, Gagné V, Ansari M, Sinnett D, Labuda D, Moghrabi A, Krajinovic M.

Blood. 2008 Apr 1;111(7):3692-700. Epub 2007 Dec 20.

41.

Genetic variation and population structure in native Americans.

Wang S, Lewis CM, Jakobsson M, Ramachandran S, Ray N, Bedoya G, Rojas W, Parra MV, Molina JA, Gallo C, Mazzotti G, Poletti G, Hill K, Hurtado AM, Labuda D, Klitz W, Barrantes R, Bortolini MC, Salzano FM, Petzl-Erler ML, Tsuneto LT, Llop E, Rothhammer F, Excoffier L, Feldman MW, Rosenberg NA, Ruiz-Linares A.

PLoS Genet. 2007 Nov;3(11):e185.

42.

[Founder effects and genetic variability in Quebec].

Moreau C, Vézina H, Labuda D.

Med Sci (Paris). 2007 Nov;23(11):1008-13. French.

43.

A protocol for the in vitro selection of specific oligonucleotide probes for high-resolution DNA typing.

Brukner I, Krajinovic M, Dascal A, Labuda D.

Nat Protoc. 2007;2(11):2807-14.

PMID:
18007616
44.

Age and origin of major Smith-Lemli-Opitz syndrome (SLOS) mutations in European populations.

Witsch-Baumgartner M, Schwentner I, Gruber M, Benlian P, Bertranpetit J, Bieth E, Chevy F, Clusellas N, Estivill X, Gasparini G, Giros M, Kelley RI, Krajewska-Walasek M, Menzel J, Miettinen T, Ogorelkova M, Rossi M, Scala I, Schinzel A, Schmidt K, Schönitzer D, Seemanova E, Sperling K, Syrrou M, Talmud PJ, Wollnik B, Krawczak M, Labuda D, Utermann G.

J Med Genet. 2008 Apr;45(4):200-9. Epub 2007 Oct 26.

PMID:
17965227
45.

Newly-isolated HPV97, related to HPV18 and 45 is frequently detected in HIV-positive men from the Montreal area.

Gorska-Flipot I, Sawick J, Gaboury LA, Krajinovic M, Labuda D, Brukner I, Rouleau D, Ghattas G, Franco EL, Coutlée F.

Int J Cancer. 2008 Mar 1;122(5):1195-7. No abstract available.

46.

Tracing genetic history of modern humans using X-chromosome lineages.

Yotova V, Lefebvre JF, Kohany O, Jurka J, Michalski R, Modiano D, Utermann G, Williams SM, Labuda D.

Hum Genet. 2007 Dec;122(5):431-43. Epub 2007 Aug 7.

PMID:
17680273
47.

Subcellular proteomics of cell differentiation: quantitative analysis of the plasma membrane proteome of Caco-2 cells.

Pshezhetsky AV, Fedjaev M, Ashmarina L, Mazur A, Budman L, Sinnett D, Labuda D, Beaulieu JF, Ménard D, Nifant'ev I, Levy E.

Proteomics. 2007 Jun;7(13):2201-15.

PMID:
17549793
48.

Hybridization assay performed at ambient temperature for typing high-risk human papillomaviruses.

Brukner I, El-Ramahi R, Sawicki J, Gorska-Flipot I, Krajinovic M, Labuda D.

J Clin Virol. 2007 Jun;39(2):113-8. Epub 2007 May 7. Erratum in: J Clin Virol. 2007 Aug;39(4):328.

PMID:
17482870
49.

An in vitro selection scheme for oligonucleotide probes to discriminate between closely related DNA sequences.

Brukner I, El-Ramahi R, Gorska-Flipot I, Krajinovic M, Labuda D.

Nucleic Acids Res. 2007;35(9):e66. Epub 2007 Apr 10.

50.

Patterns of variation in DNA segments upstream of transcription start sites.

Labuda D, Labbé C, Langlois S, Lefebvre JF, Freytag V, Moreau C, Sawicki J, Beaulieu P, Pastinen T, Hudson TJ, Sinnett D.

Hum Mutat. 2007 May;28(5):441-50.

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