Risch N - Search Results

1

Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease.

Botstein D, Risch N. Botstein D, et al. Among authors: risch n. Nat Genet. 2003 Mar;33 Suppl:228-37. doi: 10.1038/ng1090. Nat Genet. 2003. PMID: 12610532 Review.

2

A manic depressive history.

Risch N, Botstein D. Risch N, et al. Nat Genet. 1996 Apr;12(4):351-3. doi: 10.1038/ng0496-351. Nat Genet. 1996. PMID: 8630482 No abstract available.

3

A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis.

Feder JN, Gnirke A, Thomas W, Tsuchihashi Z, Ruddy DA, Basava A, Dormishian F, Domingo R Jr, Ellis MC, Fullan A, Hinton LM, Jones NL, Kimmel BE, Kronmal GS, Lauer P, Lee VK, Loeb DB, Mapa FA, McClelland E, Meyer NC, Mintier GA, Moeller N, Moore T, Morikang E, Prass CE, Quintana L, Starnes SM, Schatzman RC, Brunke KJ, Drayna DT, Risch NJ, Bacon BR, Wolff RK. Feder JN, et al. Among authors: risch nj. Nat Genet. 1996 Aug;13(4):399-408. doi: 10.1038/ng0896-399. Nat Genet. 1996. PMID: 8696333

4

The future of genetic studies of complex human diseases.

Risch N, Merikangas K. Risch N, et al. Science. 1996 Sep 13;273(5281):1516-7. doi: 10.1126/science.273.5281.1516. Science. 1996. PMID: 8801636 No abstract available.

5

Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21.

Mansfield TA, Simon DB, Farfel Z, Bia M, Tucci JR, Lebel M, Gutkin M, Vialettes B, Christofilis MA, Kauppinen-Makelin R, Mayan H, Risch N, Lifton RP. Mansfield TA, et al. Among authors: risch n. Nat Genet. 1997 Jun;16(2):202-5. doi: 10.1038/ng0697-202. Nat Genet. 1997. PMID: 9171836

6

Searching for genetic determinants in the new millennium.

Risch NJ. Risch NJ. Nature. 2000 Jun 15;405(6788):847-56. doi: 10.1038/35015718. Nature. 2000. PMID: 10866211 Review.

7

Lack of evidence for an association between alpha-adducin and blood pressure regulation in Asian populations.

Ranade K, Hsuing AC, Wu KD, Chang MS, Chen YT, Hebert J, Chen YI, Olshen R, Curb D, Dzau V, Botstein D, Cox D, Risch N. Ranade K, et al. Among authors: risch n. Am J Hypertens. 2000 Jun;13(6 Pt 1):704-9. doi: 10.1016/s0895-7061(00)00238-7. Am J Hypertens. 2000. PMID: 10912757

8

Screening a large reference sample to identify very low frequency sequence variants: comparisons between two genes.

Glatt CE, DeYoung JA, Delgado S, Service SK, Giacomini KM, Edwards RH, Risch N, Freimer NB. Glatt CE, et al. Among authors: risch n. Nat Genet. 2001 Apr;27(4):435-8. doi: 10.1038/86948. Nat Genet. 2001. PMID: 11279528

9

High-throughput genotyping with single nucleotide polymorphisms.

Ranade K, Chang MS, Ting CT, Pei D, Hsiao CF, Olivier M, Pesich R, Hebert J, Chen YD, Dzau VJ, Curb D, Olshen R, Risch N, Cox DR, Botstein D. Ranade K, et al. Among authors: risch n. Genome Res. 2001 Jul;11(7):1262-8. doi: 10.1101/gr.157801. Genome Res. 2001. PMID: 11435409 Free PMC article.

10

Genetic variation in the human urea transporter-2 is associated with variation in blood pressure.

Ranade K, Wu KD, Hwu CM, Ting CT, Pei D, Pesich R, Hebert J, Chen YD, Pratt R, Olshen R, Masaki K, Risch N, Cox DR, Botstein D. Ranade K, et al. Among authors: risch n. Hum Mol Genet. 2001 Sep 15;10(19):2157-64. doi: 10.1093/hmg/10.19.2157. Hum Mol Genet. 2001. PMID: 11590132

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