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Items: 1 to 50 of 124

1.

A Lesion on the Eye.

Cann H, Luehrs E.

Am Fam Physician. 2018 Mar 1;97(5):337-338. No abstract available.

2.

Distance from sub-Saharan Africa predicts mutational load in diverse human genomes.

Henn BM, Botigué LR, Peischl S, Dupanloup I, Lipatov M, Maples BK, Martin AR, Musharoff S, Cann H, Snyder MP, Excoffier L, Kidd JM, Bustamante CD.

Proc Natl Acad Sci U S A. 2016 Jan 26;113(4):E440-9. doi: 10.1073/pnas.1510805112. Epub 2015 Dec 28.

3.

Transcriptome sequencing from diverse human populations reveals differentiated regulatory architecture.

Martin AR, Costa HA, Lappalainen T, Henn BM, Kidd JM, Yee MC, Grubert F, Cann HM, Snyder M, Montgomery SB, Bustamante CD.

PLoS Genet. 2014 Aug 14;10(8):e1004549. doi: 10.1371/journal.pgen.1004549. eCollection 2014 Aug.

4.

The complete genome sequence of a Neanderthal from the Altai Mountains.

Prüfer K, Racimo F, Patterson N, Jay F, Sankararaman S, Sawyer S, Heinze A, Renaud G, Sudmant PH, de Filippo C, Li H, Mallick S, Dannemann M, Fu Q, Kircher M, Kuhlwilm M, Lachmann M, Meyer M, Ongyerth M, Siebauer M, Theunert C, Tandon A, Moorjani P, Pickrell J, Mullikin JC, Vohr SH, Green RE, Hellmann I, Johnson PL, Blanche H, Cann H, Kitzman JO, Shendure J, Eichler EE, Lein ES, Bakken TE, Golovanova LV, Doronichev VB, Shunkov MV, Derevianko AP, Viola B, Slatkin M, Reich D, Kelso J, Pääbo S.

Nature. 2014 Jan 2;505(7481):43-9. doi: 10.1038/nature12886. Epub 2013 Dec 18.

5.

Abrupt onset of abdominal pain. Duodenal perforation caused by indomethacin.

Singh M, Reichert P, Cann H.

J Fam Pract. 2013 Dec;62(12):749-51. No abstract available.

PMID:
24340337
6.

Positive selection in the chromosome 16 VKORC1 genomic region has contributed to the variability of anticoagulant response in humans.

Patillon B, Luisi P, Blanché H, Patin E, Cann HM, Génin E, Sabbagh A.

PLoS One. 2012;7(12):e53049. doi: 10.1371/journal.pone.0053049. Epub 2012 Dec 28.

7.

Similarity in recombination rate and linkage disequilibrium at CYP2C and CYP2D cytochrome P450 gene regions among Europeans indicates signs of selection and no advantage of using tagSNPs in population isolates.

Pimenoff VN, Laval G, Comas D, Palo JU, Gut I, Cann H, Excoffier L, Sajantila A.

Pharmacogenet Genomics. 2012 Dec;22(12):846-57. doi: 10.1097/FPC.0b013e32835a3a6d.

PMID:
23089684
8.

Consanguinity around the world: what do the genomic data of the HGDP-CEPH diversity panel tell us?

Leutenegger AL, Sahbatou M, Gazal S, Cann H, Génin E.

Eur J Hum Genet. 2011 May;19(5):583-7. doi: 10.1038/ejhg.2010.205. Epub 2011 Mar 2.

9.

Building the sequence map of the human pan-genome.

Li R, Li Y, Zheng H, Luo R, Zhu H, Li Q, Qian W, Ren Y, Tian G, Li J, Zhou G, Zhu X, Wu H, Qin J, Jin X, Li D, Cao H, Hu X, Blanche H, Cann H, Zhang X, Li S, Bolund L, Kristiansen K, Yang H, Wang J, Wang J.

Nat Biotechnol. 2010 Jan;28(1):57-63. doi: 10.1038/nbt.1596. Epub 2009 Dec 7.

PMID:
19997067
10.

Jean B Dausset, 19 October 1916-6 June 2009.

Mandel JL, Lathrop M, Cann HM.

Eur J Hum Genet. 2009 Nov;17(11):1365-6. doi: 10.1038/ejhg.2009.150. No abstract available.

11.

Worldwide human relationships inferred from genome-wide patterns of variation.

Li JZ, Absher DM, Tang H, Southwick AM, Casto AM, Ramachandran S, Cann HM, Barsh GS, Feldman M, Cavalli-Sforza LL, Myers RM.

Science. 2008 Feb 22;319(5866):1100-4. doi: 10.1126/science.1153717.

12.

Genotype, haplotype and copy-number variation in worldwide human populations.

Jakobsson M, Scholz SW, Scheet P, Gibbs JR, VanLiere JM, Fung HC, Szpiech ZA, Degnan JH, Wang K, Guerreiro R, Bras JM, Schymick JC, Hernandez DG, Traynor BJ, Simon-Sanchez J, Matarin M, Britton A, van de Leemput J, Rafferty I, Bucan M, Cann HM, Hardy JA, Rosenberg NA, Singleton AB.

Nature. 2008 Feb 21;451(7181):998-1003. doi: 10.1038/nature06742.

13.

Sequence variants of estrogen receptor beta and risk of prostate cancer in the National Cancer Institute Breast and Prostate Cancer Cohort Consortium.

Chen YC, Kraft P, Bretsky P, Ketkar S, Hunter DJ, Albanes D, Altshuler D, Andriole G, Berg CD, Boeing H, Burtt N, Bueno-de-Mesquita B, Cann H, Canzian F, Chanock S, Dunning A, Feigelson HS, Freedman M, Gaziano JM, Giovannucci E, Sánchez MJ, Haiman CA, Hallmans G, Hayes RB, Henderson BE, Hirschhorn J, Kaaks R, Key TJ, Kolonel LN, LeMarchand L, Ma J, Overvad K, Palli D, Pharaoh P, Pike M, Riboli E, Rodriguez C, Setiawan VW, Stampfer M, Stram DO, Thomas G, Thun MJ, Travis RC, Virtamo J, Trichopoulou A, Wacholder S, Weinstein SJ.

Cancer Epidemiol Biomarkers Prev. 2007 Oct;16(10):1973-81.

14.

Haplotype analysis of the HSD17B1 gene and risk of breast cancer: a comprehensive approach to multicenter analyses of prospective cohort studies.

Feigelson HS, Cox DG, Cann HM, Wacholder S, Kaaks R, Henderson BE, Albanes D, Altshuler D, Berglund G, Berrino F, Bingham S, Buring JE, Burtt NP, Calle EE, Chanock SJ, Clavel-Chapelon F, Colditz G, Diver WR, Freedman ML, Haiman CA, Hankinson SE, Hayes RB, Hirschhorn JN, Hunter D, Kolonel LN, Kraft P, LeMarchand L, Linseisen J, Modi W, Navarro C, Peeters PH, Pike MC, Riboli E, Setiawan VW, Stram DO, Thomas G, Thun MJ, Tjonneland A, Trichopoulos D.

Cancer Res. 2006 Feb 15;66(4):2468-75. Erratum in: Cancer Res. 2008 May 1;68(9):3550.

15.

The portability of tagSNPs across populations: a worldwide survey.

González-Neira A, Ke X, Lao O, Calafell F, Navarro A, Comas D, Cann H, Bumpstead S, Ghori J, Hunt S, Deloukas P, Dunham I, Cardon LR, Bertranpetit J.

Genome Res. 2006 Mar;16(3):323-30. Epub 2006 Feb 8.

16.

A candidate gene approach to searching for low-penetrance breast and prostate cancer genes.

Hunter DJ, Riboli E, Haiman CA, Albanes D, Altshuler D, Chanock SJ, Haynes RB, Henderson BE, Kaaks R, Stram DO, Thomas G, Thun MJ, Blanché H, Buring JE, Burtt NP, Calle EE, Cann H, Canzian F, Chen YC, Colditz GA, Cox DG, Dunning AM, Feigelson HS, Freedman ML, Gaziano JM, Giovannucci E, Hankinson SE, Hirschhorn JN, Hoover RN, Key T, Kolonel LN, Kraft P, Le Marchand L, Liu S, Ma J, Melnick S, Pharaoh P, Pike MC, Rodriguez C, Setiawan VW, Stampfer MJ, Trapido E, Travis R, Virtamo J, Wacholder S, Willett WC; National Cancer Institute Breast and Prostate Cancer Cohort Consortium.

Nat Rev Cancer. 2005 Dec;5(12):977-85. doi: 10.1038/nrc1754. Review.

PMID:
16341085
17.

Genetic variation in the HSD17B1 gene and risk of prostate cancer.

Kraft P, Pharoah P, Chanock SJ, Albanes D, Kolonel LN, Hayes RB, Altshuler D, Andriole G, Berg C, Boeing H, Burtt NP, Bueno-de-Mesquita B, Calle EE, Cann H, Canzian F, Chen YC, Crawford DE, Dunning AM, Feigelson HS, Freedman ML, Gaziano JM, Giovannucci E, Gonzalez CA, Haiman CA, Hallmans G, Henderson BE, Hirschhorn JN, Hunter DJ, Kaaks R, Key T, Le Marchand L, Ma J, Overvad K, Palli D, Pike MC, Riboli E, Rodriguez C, Setiawan WV, Stampfer MJ, Stram DO, Thomas G, Thun MJ, Travis R, Trichopoulou A, Virtamo J, Wacholder S.

PLoS Genet. 2005 Nov;1(5):e68. Epub 2005 Nov 25.

18.

The heritage of pathogen pressures and ancient demography in the human innate-immunity CD209/CD209L region.

Barreiro LB, Patin E, Neyrolles O, Cann HM, Gicquel B, Quintana-Murci L.

Am J Hum Genet. 2005 Nov;77(5):869-86. Epub 2005 Sep 29.

19.

Geographic stratification of linkage disequilibrium: a worldwide population study in a region of chromosome 22.

González-Neira A, Calafell F, Navarro A, Lao O, Cann H, Comas D, Bertranpetit J.

Hum Genomics. 2004 Nov;1(6):399-409.

20.

The 3' UTR elements of P. gallinaceum protein Pgs28 are functionally distinct from those of human cells.

Shue P, Brown SV, Cann H, Singer EF, Appleby S, Golightly LM.

Mol Biochem Parasitol. 2004 Oct;137(2):355-9. No abstract available.

PMID:
15383307
21.
22.

A national DNA bank in The Gambia, West Africa, and genomic research in developing countries.

Sirugo G, Schim van der Loeff M, Sam O, Nyan O, Pinder M, Hill AV, Kwiatkowski D, Prentice A, de Toma C, Cann HM, Diatta M, Jallow M, Morgan G, Clarke M, Corrah T, Whittle H, McAdam K.

Nat Genet. 2004 Aug;36(8):785-6. No abstract available.

PMID:
15284842
23.

Read all about it: The Lancet's Paper of the Year, 2003.

Horton R, Rosenberg NA, Pritchard JK, Weber JL, Cann HM, Kidd KK, Zhivotovsky LA, Feldman MW.

Lancet. 2003 Dec 20;362(9401):2101-3. No abstract available.

PMID:
14697815
24.

A 3.9-centimorgan-resolution human single-nucleotide polymorphism linkage map and screening set.

Matise TC, Sachidanandam R, Clark AG, Kruglyak L, Wijsman E, Kakol J, Buyske S, Chui B, Cohen P, de Toma C, Ehm M, Glanowski S, He C, Heil J, Markianos K, McMullen I, Pericak-Vance MA, Silbergleit A, Stein L, Wagner M, Wilson AF, Winick JD, Winn-Deen ES, Yamashiro CT, Cann HM, Lai E, Holden AL.

Am J Hum Genet. 2003 Aug;73(2):271-84. Epub 2003 Jul 3.

25.

Irruption of genomics in the search for disease related genes.

Thomas G, Cann H.

Gut. 2003 May;52 Suppl 2:ii1-5. Review.

26.

Genetic structure of human populations.

Rosenberg NA, Pritchard JK, Weber JL, Cann HM, Kidd KK, Zhivotovsky LA, Feldman MW.

Science. 2002 Dec 20;298(5602):2381-5.

27.

A human genome diversity cell line panel.

Cann HM, de Toma C, Cazes L, Legrand MF, Morel V, Piouffre L, Bodmer J, Bodmer WF, Bonne-Tamir B, Cambon-Thomsen A, Chen Z, Chu J, Carcassi C, Contu L, Du R, Excoffier L, Ferrara GB, Friedlaender JS, Groot H, Gurwitz D, Jenkins T, Herrera RJ, Huang X, Kidd J, Kidd KK, Langaney A, Lin AA, Mehdi SQ, Parham P, Piazza A, Pistillo MP, Qian Y, Shu Q, Xu J, Zhu S, Weber JL, Greely HT, Feldman MW, Thomas G, Dausset J, Cavalli-Sforza LL.

Science. 2002 Apr 12;296(5566):261-2. No abstract available.

PMID:
11954565
28.

Report of the Fourth International Chromosome 6 Workshop 1999. 10-12 June 1999. Cambridge, UK. Abstracts.

Mungall AJ, Beck S, Cann HM, Dunham I, Trowsdale J, Ziegler A.

Cytogenet Cell Genet. 2000;88(3-4):173-96. No abstract available.

PMID:
10828583
29.

Human genome diversity.

Cann HM.

C R Acad Sci III. 1998 Jun;321(6):443-6.

PMID:
9769857
30.

Anticipation in schizophrenia: no evidence of expanded CAG/CTG repeat sequences in French families and sporadic cases.

Laurent C, Zander C, Thibaut F, Bonnet-Brilhault F, Chavand O, Jay M, Samolyk D, Petit M, Martinez M, Campion D, Néri C, Mallet J, Cann H.

Am J Med Genet. 1998 Jul 10;81(4):342-6.

PMID:
9674982
31.

CAG repeat sequences in bipolar affective disorder: no evidence for association in a French population.

Zander C, Schürhoff F, Laurent C, Chavand O, Bellivier F, Samolyk D, Leboyer M, Allilaire JF, Cann H, Néri C, Mallet J.

Am J Med Genet. 1998 Jul 10;81(4):338-41.

PMID:
9674981
32.

CAG/CTG and CGG/GCC repeats in human brain reference cDNAs: outcome in searching for new dynamic mutations.

Albanese V, Holbert S, Saada C, Meier-Ewert S, Lebre AS, Moriniere S, Bougueleret L, Le Gall I, Weissenbach J, Lennon G, Lehrach H, Cohen D, Cann HM, Neri C.

Genomics. 1998 Feb 1;47(3):414-8.

PMID:
9480757
33.

After the genome database.

Cann HM.

Science. 1998 Mar 13;279(5357):1611-2. No abstract available.

PMID:
9518369
34.

Guidelines for human gene nomenclature (1997). HUGO Nomenclature Committee.

White JA, McAlpine PJ, Antonarakis S, Cann H, Eppig JT, Frazer K, Frezal J, Lancet D, Nahmias J, Pearson P, Peters J, Scott A, Scott H, Spurr N, Talbot C Jr, Povey S.

Genomics. 1997 Oct 15;45(2):468-71. No abstract available.

PMID:
9344684
35.

Third single chromosome 6 workshop: meeting report.

Beck S, Cann HM, Campbell RD, Dunham I, Inoko H, Jazwinska EC, Ragoussis J, Trowsdale J, Ziegler A.

DNA Seq. 1997;8(3):113-29. No abstract available.

PMID:
10668955
36.

Survey of CAG/CTG repeats in human cDNAs representing new genes: candidates for inherited neurological disorders.

Néri C, Albanèse V, Lebre AS, Holbert S, Saada C, Bougueleret L, Meier-Ewert S, Le Gall I, Millasseau P, Bui H, Giudicelli C, Massart C, Guillou S, Gervy P, Poullier E, Rigault P, Weissenbach J, Lennon G, Chumakov I, Dausset J, Lehrach H, Cohen D, Cann HM.

Hum Mol Genet. 1996 Jul;5(7):1001-9.

PMID:
8817338
37.
38.

Detection by hybridization of trinucleotide repeat sequences in yeast artificial chromosomes.

Nemani M, Bellanné-Chantelot C, Cohen D, Cann HM.

Biotechniques. 1995 Oct;19(4):584-7. No abstract available.

PMID:
8777051
39.

Marked phenotypic heterogeneity associated with expansion of a CAG repeat sequence at the spinocerebellar ataxia 3/Machado-Joseph disease locus.

Cancel G, Abbas N, Stevanin G, Dürr A, Chneiweiss H, Néri C, Duyckaerts C, Penet C, Cann HM, Agid Y, et al.

Am J Hum Genet. 1995 Oct;57(4):809-16.

40.

The gene for spinal cerebellar ataxia 3 (SCA3) is located in a region of approximately 3 cM on chromosome 14q24.3-q32.2.

Stevanin G, Cancel G, Dürr A, Chneiweiss H, Dubourg O, Weissenbach J, Cann HM, Agid Y, Brice A.

Am J Hum Genet. 1995 Jan;56(1):193-201.

41.

Our genetic patrimony.

Dausset J, Cann H.

Science. 1994 Sep 30;265(5181):1991. No abstract available.

PMID:
7916484
42.

A YAC contig in 6p23 based on sequence tagged sites.

Nemani M, Cherif D, Chesne H, Pelandakis M, Ougen P, Berger R, Weissenbach J, Le Paslier D, Cohen D, Cann HM.

Genomics. 1994 Jul 15;22(2):388-96.

PMID:
7806226
43.

Report of the Second International Workshop on Human Chromosome 6.

Volz A, Boyle JM, Cann HM, Cottingham RW, Orr HT, Ziegler A.

Genomics. 1994 May 15;21(2):464-72. No abstract available.

PMID:
8088851
44.

Endothelin 1 is not a candidate gene for spinal cerebellar ataxia 1.

Cancel G, Khati C, Stevanin G, Pages JC, Agid Y, Brice A, Cann HM.

Hum Mol Genet. 1993 Sep;2(9):1477-9. No abstract available.

PMID:
8242075
45.

Genetic heterogeneity of autosomal dominant cerebellar ataxia type 1: clinical and genetic analysis of 10 French families.

Khati C, Stevanin G, Durr A, Chneiweiss H, Belal S, Seck A, Cann H, Brice A, Agid Y.

Neurology. 1993 Jun;43(6):1131-7.

PMID:
8170557
46.

A short tandem repeat polymorphism at the endothelin 1 (EDN1) locus.

Pages JC, Drieu C, Blanché H, Beckmann J, Cann HM.

Hum Mol Genet. 1993 Jan;2(1):90. No abstract available.

PMID:
8490632
47.

Linkage studies in dominantly inherited ataxias.

Zoghbi HY, Frontali M, Orr HT, Sandkuijl L, Cann H, Sasaki H, Chamberlain S, Terrenato L, Rich SS.

Adv Neurol. 1993;61:133-7. Review. No abstract available.

PMID:
8421963
48.

CEPH maps.

Cann HM.

Curr Opin Genet Dev. 1992 Jun;2(3):393-9. Review.

PMID:
1504612
49.

Genetic mapping of three human homologues of murine t-complex genes localizes TCP10 to 6q27, 15 cM distal to TCP1 and PLG.

Blanché H, Wright LG, Vergnaud G, de Gouyon B, Lauthier V, Silver LM, Dausset J, Cann HM, Spielman RS.

Genomics. 1992 Apr;12(4):826-8.

PMID:
1572657
50.

The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps telomeric to the HLA complex and is closely linked to the D6S89 locus in three large kindreds.

Zoghbi HY, Jodice C, Sandkuijl LA, Kwiatkowski TJ Jr, McCall AE, Huntoon SA, Lulli P, Spadaro M, Litt M, Cann HM, et al.

Am J Hum Genet. 1991 Jul;49(1):23-30.

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