Foroud T - Search Results

1

Heterogeneity in hereditary pancreatitis.

Dasouki MJ, Cogan J, Summar ML, Neblitt W 3rd, Foroud T, Koller D, Phillips JA 3rd. Dasouki MJ, et al. Among authors: foroud t. Am J Med Genet. 1998 Apr 28;77(1):47-53. Am J Med Genet. 1998. PMID: 9557894

2

Localization of the gene for familial primary pulmonary hypertension to chromosome 2q31-32.

Nichols WC, Koller DL, Slovis B, Foroud T, Terry VH, Arnold ND, Siemieniak DR, Wheeler L, Phillips JA 3rd, Newman JH, Conneally PM, Ginsburg D, Loyd JE. Nichols WC, et al. Among authors: foroud t. Nat Genet. 1997 Mar;15(3):277-80. doi: 10.1038/ng0397-277. Nat Genet. 1997. PMID: 9054941

3

Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17.

Murrell JR, Koller D, Foroud T, Goedert M, Spillantini MG, Edenberg HJ, Farlow MR, Ghetti B. Murrell JR, et al. Among authors: foroud t. Am J Hum Genet. 1997 Nov;61(5):1131-8. doi: 10.1086/301594. Am J Hum Genet. 1997. PMID: 9345089 Free PMC article.

4

Suggestive evidence of a locus on chromosome 10p using the NIMH genetics initiative bipolar affective disorder pedigrees.

Foroud T, Castelluccio PF, Koller DL, Edenberg HJ, Miller M, Bowman E, Rau NL, Smiley C, Rice JP, Goate A, Armstrong C, Bierut LJ, Reich T, Detera-Wadleigh SD, Goldin LR, Badner JA, Guroff JJ, Gershon ES, McMahon FJ, Simpson S, MacKinnon D, McInnis M, Stine OC, DePaulo JR, Blehar MC, Nurnberger JI Jr. Foroud T, et al. Am J Med Genet. 2000 Feb 7;96(1):18-23. Am J Med Genet. 2000. PMID: 10686547

5

Genetic anticipation and abnormal gender ratio at birth in familial primary pulmonary hypertension.

Loyd JE, Butler MG, Foroud TM, Conneally PM, Phillips JA 3rd, Newman JH. Loyd JE, et al. Among authors: foroud tm. Am J Respir Crit Care Med. 1995 Jul;152(1):93-7. doi: 10.1164/ajrccm.152.1.7599869. Am J Respir Crit Care Med. 1995. PMID: 7599869 Free PMC article.

6

Locus heterogeneity of autosomal dominant osteopetrosis (ADO).

White KE, Koller DL, Takacs I, Buckwalter KA, Foroud T, Econs MJ. White KE, et al. Among authors: foroud t. J Clin Endocrinol Metab. 1999 Mar;84(3):1047-51. doi: 10.1210/jcem.84.3.5578. J Clin Endocrinol Metab. 1999. PMID: 10084593

7

Nonparametric linkage and family-based association studies of a simulated complex disorder.

Koller DL, Balding J, Foroud T. Koller DL, et al. Among authors: foroud t. Genet Epidemiol. 1999;17 Suppl 1:S627-32. doi: 10.1002/gepi.13701707102. Genet Epidemiol. 1999. PMID: 10597504

8

The presence of genetic anticipation suggests that the molecular basis of familial primary pulmonary hypertension may be trinucleotide repeat expansion.

Loyd JE, Slovis B, Phillips JA 3rd, Butler MG, Foroud TM, Conneally PM, Newman JH. Loyd JE, et al. Among authors: foroud tm. Chest. 1997 Jun;111(6 Suppl):82S-83S. doi: 10.1378/chest.111.6_supplement.82s. Chest. 1997. PMID: 9184540 Free PMC article. No abstract available.

9

Alcoholism susceptibility loci: confirmation studies in a replicate sample and further mapping.

Foroud T, Edenberg HJ, Goate A, Rice J, Flury L, Koller DL, Bierut LJ, Conneally PM, Nurnberger JI, Bucholz KK, Li TK, Hesselbrock V, Crowe R, Schuckit M, Porjesz B, Begleiter H, Reich T. Foroud T, et al. Alcohol Clin Exp Res. 2000 Jul;24(7):933-45. Alcohol Clin Exp Res. 2000. PMID: 10923994 Clinical Trial.

10

Use of variable marker density, principal components, and neural networks in the dissection of disease etiology.

Pankratz N, Kirkwood SC, Flury L, Koller DL, Foroud T. Pankratz N, et al. Among authors: foroud t. Genet Epidemiol. 2001;21 Suppl 1:S732-7. doi: 10.1002/gepi.2001.21.s1.s732. Genet Epidemiol. 2001. PMID: 11793770

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