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Items: 18

1.

Returning genetic research results to individuals: points-to-consider.

Renegar G, Webster CJ, Stuerzebecher S, Harty L, Ide SE, Balkite B, Rogalski-Salter TA, Cohen N, Spear BB, Barnes DM, Brazell C.

Bioethics. 2006 Feb;20(1):24-36. Review.

PMID:
16680905
2.

The G209A mutation in the alpha-synuclein gene in Brazilian families with Parkinson's disease.

Teive HA, Raskin S, Iwamoto FM, Germiniani FM, Baran MH, Werneck LC, Allan N, Quagliato E, Leroy E, Ide SE, Polymeropoulos MH.

Arq Neuropsiquiatr. 2001 Sep;59(3-B):722-4.

3.

Mutations in a new gene in Ellis-van Creveld syndrome and Weyers acrodental dysostosis.

Ruiz-Perez VL, Ide SE, Strom TM, Lorenz B, Wilson D, Woods K, King L, Francomano C, Freisinger P, Spranger S, Marino B, Dallapiccola B, Wright M, Meitinger T, Polymeropoulos MH, Goodship J.

Nat Genet. 2000 Mar;24(3):283-6. Erratum in: Nat Genet 2000 May;25(1):125.

PMID:
10700184
4.

Genomic structure and localization of the human protein phosphatase 2A BRgamma regulatory subunit.

Torres R, Ide SE, Dehejia A, Baras A, Polymeropoulos MH.

DNA Res. 1999 Oct 29;6(5):323-7.

PMID:
10574460
5.

Contig map of the Parkinson's disease region on 4q21-q23.

Lavedan C, Dehejia A, Pike B, Dutra A, Leroy E, Ide SE, Root H, Rubenstein J, Boyer RL, Chandrasekharappa S, Makalowska I, Nussbaum RL, Polymeropoulos MH.

DNA Res. 1998 Feb 28;5(1):19-23.

PMID:
9628579
6.

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease.

Polymeropoulos MH, Lavedan C, Leroy E, Ide SE, Dehejia A, Dutra A, Pike B, Root H, Rubenstein J, Boyer R, Stenroos ES, Chandrasekharappa S, Athanassiadou A, Papapetropoulos T, Johnson WG, Lazzarini AM, Duvoisin RC, Di Iorio G, Golbe LI, Nussbaum RL.

Science. 1997 Jun 27;276(5321):2045-7.

7.

Evidence for a new spinocerebellar ataxia locus.

Higgins JJ, Pho LT, Ide SE, Nee LE, Polymeropoulos MH.

Mov Disord. 1997 May;12(3):412-7.

PMID:
9159738
8.

Lack of mutations in the biotin-binding region of the pyruvate carboxylase (PC) gene in a family with partial PC deficiency.

Higgins JJ, Ide SE, Oghalai JS, Polymeropoulos MH.

Clin Biochem. 1997 Feb;30(1):79-81. No abstract available.

PMID:
9056115
9.

Brachydactyly type C gene maps to human chromsome 12q24.

Polymeropoulos MH, Ide SE, Magyari T, Francomano CA.

Genomics. 1996 Nov 15;38(1):45-50.

PMID:
8954778
10.

Mapping of a gene for Parkinson's disease to chromosome 4q21-q23.

Polymeropoulos MH, Higgins JJ, Golbe LI, Johnson WG, Ide SE, Di Iorio G, Sanges G, Stenroos ES, Pho LT, Schaffer AA, Lazzarini AM, Nussbaum RL, Duvoisin RC.

Science. 1996 Nov 15;274(5290):1197-9.

PMID:
8895469
11.

Linkage and cytogenetic mapping of a CAG repeat containing human cDNA to 3p24.2-p22.

Polymeropoulos MH, Ide SE, Becker K, Naylor SL.

Cancer Genet Cytogenet. 1996 Nov;92(1):46-9.

PMID:
8956871
12.

Exclusion of the MSX1 homeobox gene as the gene for the Ellis van Creveld syndrome in the Amish.

Ide SE, Ortiz de Luna RI, Francomano CA, Polymeropoulos MH.

Hum Genet. 1996 Nov;98(5):572-5.

PMID:
8882877
13.

A gene map of the human genome.

Schuler GD, Boguski MS, Stewart EA, Stein LD, Gyapay G, Rice K, White RE, Rodriguez-Tomé P, Aggarwal A, Bajorek E, Bentolila S, Birren BB, Butler A, Castle AB, Chiannilkulchai N, Chu A, Clee C, Cowles S, Day PJ, Dibling T, Drouot N, Dunham I, Duprat S, East C, Edwards C, Fan JB, Fang N, Fizames C, Garrett C, Green L, Hadley D, Harris M, Harrison P, Brady S, Hicks A, Holloway E, Hui L, Hussain S, Louis-Dit-Sully C, Ma J, MacGilvery A, Mader C, Maratukulam A, Matise TC, McKusick KB, Morissette J, Mungall A, Muselet D, Nusbaum HC, Page DC, Peck A, Perkins S, Piercy M, Qin F, Quackenbush J, Ranby S, Reif T, Rozen S, Sanders C, She X, Silva J, Slonim DK, Soderlund C, Sun WL, Tabar P, Thangarajah T, Vega-Czarny N, Vollrath D, Voyticky S, Wilmer T, Wu X, Adams MD, Auffray C, Walter NA, Brandon R, Dehejia A, Goodfellow PN, Houlgatte R, Hudson JR Jr, Ide SE, Iorio KR, Lee WY, Seki N, Nagase T, Ishikawa K, Nomura N, Phillips C, Polymeropoulos MH, Sandusky M, Schmitt K, Berry R, Swanson K, Torres R, Venter JC, Sikela JM, Beckmann JS, Weissenbach J, Myers RM, Cox DR, James MR, Bentley D, Deloukas P, Lander ES, Hudson TJ.

Science. 1996 Oct 25;274(5287):540-6. Review.

PMID:
8849440
14.

The gene for the Ellis-van Creveld syndrome is located on chromosome 4p16.

Polymeropoulos MH, Ide SE, Wright M, Goodship J, Weissenbach J, Pyeritz RE, Da Silva EO, Ortiz De Luna RI, Francomano CA.

Genomics. 1996 Jul 1;35(1):1-5.

PMID:
8661097
15.

Mutations in American families with spinocerebellar ataxia (SCA) type 3: SCA3 is allelic to Machado-Joseph disease.

Higgins JJ, Nee LE, Vasconcelos O, Ide SE, Lavedan C, Goldfarb LG, Polymeropoulos MH.

Neurology. 1996 Jan;46(1):208-13.

PMID:
8559377
16.

The gene for pycnodysostosis maps to human chromosome 1cen-q21.

Polymeropoulos MH, Ortiz De Luna RI, Ide SE, Torres R, Rubenstein J, Francomano CA.

Nat Genet. 1995 Jun;10(2):238-9.

PMID:
7663522
17.

Dinucleotide repeat polymorphism at the D11S982E locus.

Xiao H, Ide SE, Merril CR, Polymeropoulos MH.

Hum Mol Genet. 1993 Jul;2(7):1081. No abstract available.

PMID:
8364557
18.

Dinucleotide repeat polymorphism at the D14S99E locus.

Polymeropoulos MH, Xiao H, Ide SE, Merril CR.

Hum Mol Genet. 1993 Apr;2(4):490. No abstract available.

PMID:
8504315

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