Risch N - Search Results

1

Lack of association between HoxA1 and HoxB1 gene variants and autism in 110 multiplex families.

Li J, Tabor HK, Nguyen L, Gleason C, Lotspeich LJ, Spiker D, Risch N, Myers RM. Li J, et al. Among authors: risch n. Am J Med Genet. 2002 Jan 8;114(1):24-30. doi: 10.1002/ajmg.1618. Am J Med Genet. 2002. PMID: 11840501

2

Autism and the X chromosome. Multipoint sib-pair analysis.

Hallmayer J, Hebert JM, Spiker D, Lotspeich L, McMahon WM, Petersen PB, Nicholas P, Pingree C, Lin AA, Cavalli-Sforza LL, Risch N, Ciaranello RD. Hallmayer J, et al. Among authors: risch n. Arch Gen Psychiatry. 1996 Nov;53(11):985-9. doi: 10.1001/archpsyc.1996.01830110021003. Arch Gen Psychiatry. 1996. PMID: 8911221

3

A genomic screen of autism: evidence for a multilocus etiology.

Risch N, Spiker D, Lotspeich L, Nouri N, Hinds D, Hallmayer J, Kalaydjieva L, McCague P, Dimiceli S, Pitts T, Nguyen L, Yang J, Harper C, Thorpe D, Vermeer S, Young H, Hebert J, Lin A, Ferguson J, Chiotti C, Wiese-Slater S, Rogers T, Salmon B, Nicholas P, Petersen PB, Pingree C, McMahon W, Wong DL, Cavalli-Sforza LL, Kraemer HC, Myers RM. Risch N, et al. Am J Hum Genet. 1999 Aug;65(2):493-507. doi: 10.1086/302497. Am J Hum Genet. 1999. PMID: 10417292 Free PMC article.

4

Exclusion of linkage to the HLA region in ninety multiplex sibships with autism.

Rogers T, Kalaydjieva L, Hallmayer J, Petersen PB, Nicholas P, Pingree C, McMahon WM, Spiker D, Lotspeich L, Kraemer H, McCague P, Dimiceli S, Nouri N, Peachy T, Yang J, Hinds D, Risch N, Myers RM. Rogers T, et al. Among authors: risch n. J Autism Dev Disord. 1999 Jun;29(3):195-201. doi: 10.1023/a:1023075904742. J Autism Dev Disord. 1999. PMID: 10425582

5

Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism.

Salmon B, Hallmayer J, Rogers T, Kalaydjieva L, Petersen PB, Nicholas P, Pingree C, McMahon W, Spiker D, Lotspeich L, Kraemer H, McCague P, Dimiceli S, Nouri N, Pitts T, Yang J, Hinds D, Myers RM, Risch N. Salmon B, et al. Among authors: risch n. Am J Med Genet. 1999 Oct 15;88(5):551-6. Am J Med Genet. 1999. PMID: 10490715

6

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

7

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

8

Birth order effects on nonverbal IQ scores in autism multiplex families.

Spiker D, Lotspeich LJ, Dimiceli S, Szatmari P, Myers RM, Risch N. Spiker D, et al. Among authors: risch n. J Autism Dev Disord. 2001 Oct;31(5):449-60. doi: 10.1023/a:1012217807469. J Autism Dev Disord. 2001. PMID: 11794410

9

Behavioral phenotypic variation in autism multiplex families: evidence for a continuous severity gradient.

Spiker D, Lotspeich LJ, Dimiceli S, Myers RM, Risch N. Spiker D, et al. Among authors: risch n. Am J Med Genet. 2002 Mar 8;114(2):129-36. doi: 10.1002/ajmg.10188. Am J Med Genet. 2002. PMID: 11857572

10

Candidate-gene approaches for studying complex genetic traits: practical considerations.

Tabor HK, Risch NJ, Myers RM. Tabor HK, et al. Nat Rev Genet. 2002 May;3(5):391-7. doi: 10.1038/nrg796. Nat Rev Genet. 2002. PMID: 11988764 Review.

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