Lindblad K - Search Results

1

Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease.

Rioux JD, Daly MJ, Silverberg MS, Lindblad K, Steinhart H, Cohen Z, Delmonte T, Kocher K, Miller K, Guschwan S, Kulbokas EJ, O'Leary S, Winchester E, Dewar K, Green T, Stone V, Chow C, Cohen A, Langelier D, Lapointe G, Gaudet D, Faith J, Branco N, Bull SB, McLeod RS, Griffiths AM, Bitton A, Greenberg GR, Lander ES, Siminovitch KA, Hudson TJ. Rioux JD, et al. Among authors: lindblad k. Nat Genet. 2001 Oct;29(2):223-8. doi: 10.1038/ng1001-223. Nat Genet. 2001. PMID: 11586304

2

Growing triplet repeats.

Lindblad K, Zander C, Schalling M, Hudson T. Lindblad K, et al. Nat Genet. 1994 Jun;7(2):124. doi: 10.1038/ng0694-124. Nat Genet. 1994. PMID: 7920627 No abstract available.

3

Mutation detection in Machado-Joseph disease using repeat expansion detection.

Lindblad K, Lunkes A, Maciel P, Stevanin G, Zander C, Klockgether T, Ratzlaff T, Brice A, Rouleau GA, Hudson T, Auburger G, Schalling M. Lindblad K, et al. Mol Med. 1996 Jan;2(1):77-85. Mol Med. 1996. PMID: 8900536 Free PMC article.

4

Genetic survival analysis of age-at-onset of bipolar disorder: evidence for anticipation or cohort effect in families.

Visscher PM, Yazdi MH, Jackson AD, Schalling M, Lindblad K, Yuan QP, Porteous D, Muir WJ, Blackwood DH. Visscher PM, et al. Among authors: lindblad k. Psychiatr Genet. 2001 Sep;11(3):129-37. doi: 10.1097/00041444-200109000-00004. Psychiatr Genet. 2001. PMID: 11702054

5

Familial periodic cerebellar ataxia without myokymia maps to a 19-cM region on 19p13.

Teh BT, Silburn P, Lindblad K, Betz R, Boyle R, Schalling M, Larsson C. Teh BT, et al. Among authors: lindblad k. Am J Hum Genet. 1995 Jun;56(6):1443-9. Am J Hum Genet. 1995. PMID: 7762567 Free PMC article.

6

A triplet repeat on 17q accounts for most expansions detected by the repeat-expansion-detection technique.

Sidransky E, Burgess C, Ikeuchi T, Lindblad K, Long RT, Philibert RA, Rapoport J, Schalling M, Tsuji S, Ginns EI. Sidransky E, et al. Among authors: lindblad k. Am J Hum Genet. 1998 Jun;62(6):1548-51. doi: 10.1086/301876. Am J Hum Genet. 1998. PMID: 9585604 Free PMC article. No abstract available.

7

Clinical implications of unstable DNA repeat sequences.

Lindblad K, Schalling M. Lindblad K, et al. Acta Paediatr. 1996 Mar;85(3):265-71. doi: 10.1111/j.1651-2227.1996.tb14011.x. Acta Paediatr. 1996. PMID: 8695977 Review.

8

Multivariate analysis of factors influencing repeat expansion detection.

Zander C, Thelaus J, Lindblad K, Karlsson M, Sjöberg K, Schalling M. Zander C, et al. Among authors: lindblad k. Genome Res. 1998 Oct;8(10):1085-94. doi: 10.1101/gr.8.10.1085. Genome Res. 1998. PMID: 9799795 Free PMC article.

9

Expanded repeat sequences and disease.

Lindblad K, Schalling M. Lindblad K, et al. Semin Neurol. 1999;19(3):289-99. doi: 10.1055/s-2008-1040845. Semin Neurol. 1999. PMID: 12194385 Review.

10

No evidence for long CAG/CTG repeats in families with spastic paraplegia linked to chromosome 2p21-24.

Zander C, Yuan QP, Lindblad K, Stevanin G, Dürr A, Davoine CS, Hazan J, Fontaine B, Brice A, Schalling M. Zander C, et al. Among authors: lindblad k. Neurosci Lett. 2000 Jan 21;279(1):41-4. doi: 10.1016/s0304-3940(99)00946-5. Neurosci Lett. 2000. PMID: 10670783

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