Feingold J - Search Results

1

Evidence for digenic inheritance in a family with both febrile convulsions and temporal lobe epilepsy implicating chromosomes 18qter and 1q25-q31.

Baulac S, Picard F, Herman A, Feingold J, Genin E, Hirsch E, Prud'homme JF, Baulac M, Brice A, LeGuern E. Baulac S, et al. Among authors: feingold j. Ann Neurol. 2001 Jun;49(6):786-92. doi: 10.1002/ana.1014. Ann Neurol. 2001. PMID: 11409431

2

A locus for simple pure febrile seizures maps to chromosome 6q22-q24.

Nabbout R, Prud'homme JF, Herman A, Feingold J, Brice A, Dulac O, LeGuern E. Nabbout R, et al. Among authors: feingold j. Brain. 2002 Dec;125(Pt 12):2668-80. doi: 10.1093/brain/awf281. Brain. 2002. PMID: 12429594

3

Phenotypic variability in autosomal dominant cerebellar ataxia type I is unrelated to genetic heterogeneity.

Dürr A, Chneiweiss H, Khati C, Stevanin G, Cancel G, Feingold J, Agid Y, Brice A. Dürr A, et al. Among authors: feingold j. Brain. 1993 Dec;116 ( Pt 6):1497-508. doi: 10.1093/brain/116.6.1497. Brain. 1993. PMID: 8293283

4

Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study.

Philippe A, Martinez M, Guilloud-Bataille M, Gillberg C, Råstam M, Sponheim E, Coleman M, Zappella M, Aschauer H, Van Maldergem L, Penet C, Feingold J, Brice A, Leboyer M. Philippe A, et al. Among authors: feingold j. Hum Mol Genet. 1999 May;8(5):805-12. doi: 10.1093/hmg/8.5.805. Hum Mol Genet. 1999. PMID: 10196369

5

Are cognitive changes the first symptoms of Huntington's disease? A study of gene carriers.

Hahn-Barma V, Deweer B, Dürr A, Dodé C, Feingold J, Pillon B, Agid Y, Brice A, Dubois B. Hahn-Barma V, et al. Among authors: feingold j. J Neurol Neurosurg Psychiatry. 1998 Feb;64(2):172-7. doi: 10.1136/jnnp.64.2.172. J Neurol Neurosurg Psychiatry. 1998. PMID: 9489526 Free PMC article. Clinical Trial.

6

Low disease risk in relatives of north african lrrk2 Parkinson disease patients.

Troiano AR, Elbaz A, Lohmann E, Belarbi S, Vidailhet M, Bonnet AM, Lesage S, Pollak P, Cazeneuve C, Borg M, Feingold J, Dürr A, Tazir M, Brice A; French Parkinson Disease Genetic Study Group. Troiano AR, et al. Among authors: feingold j. Neurology. 2010 Sep 21;75(12):1118-9. doi: 10.1212/WNL.0b013e3181f39a2e. Neurology. 2010. PMID: 20855856 No abstract available.

7

Identifying modifier genes of monogenic disease: strategies and difficulties.

Génin E, Feingold J, Clerget-Darpoux F. Génin E, et al. Among authors: feingold j. Hum Genet. 2008 Nov;124(4):357-68. doi: 10.1007/s00439-008-0560-2. Epub 2008 Sep 11. Hum Genet. 2008. PMID: 18784943 Free PMC article. Review.

8

Huntington's disease in French families: CAG repeat expansion and linkage disequilibrium analysis.

Dodé C, Dürr A, Pêcheux C, Mouret JF, Belal S, Bachner L, Agid Y, Kaplan JC, Brice A, Feingold J. Dodé C, et al. Among authors: feingold j. C R Acad Sci III. 1993 Nov;316(11):1374-80. C R Acad Sci III. 1993. PMID: 8087617

9

Lack of association of angiotensin I-converting enzyme gene polymorphism and premature myocardial infarction in Mauritian Indians.

Ramasawmy R, Manraj M, Kotea N, Shun NK, Genin E, Feingold J, Krishnamoorthy R, Baligadoo S. Ramasawmy R, et al. Among authors: feingold j. Clin Genet. 1996 Dec;50(6):551-4. doi: 10.1111/j.1399-0004.1996.tb02737.x. Clin Genet. 1996. PMID: 9147898

10

The involvement of the trans-generational effect in the high incidence of the hydatidiform mole in Africa.

Coullin P, Diatta AL, Boufettal H, Feingold J, Leguern E, Candelier JJ. Coullin P, et al. Among authors: feingold j. Placenta. 2015 Jan;36(1):48-51. doi: 10.1016/j.placenta.2014.10.017. Epub 2014 Nov 8. Placenta. 2015. PMID: 25468544

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