Sobell J - Search Results

1

Eight novel polymorphisms in the dystrophin gene of African-Americans: the rate of polymorphism is high.

Lindor NM, Sommer SS, Sobell J, Heston L, Thibodeau SN. Lindor NM, et al. Among authors: sobell j. Hum Mutat. 1993;2(6):485-8. doi: 10.1002/humu.1380020610. Hum Mutat. 1993. PMID: 7906594 No abstract available.

2

Screening the dystrophin gene suggests a high rate of polymorphism in general but no exonic deletions in schizophrenics.

Lindor NM, Sobell JL, Heston LL, Thibodeau SN, Sommer SS. Lindor NM, et al. Among authors: sobell jl. Am J Med Genet. 1994 Mar 15;54(1):1-4. doi: 10.1002/ajmg.1320540102. Am J Med Genet. 1994. PMID: 7909988

3

A common exonic polymorphism in the human D5 dopamine receptor gene.

Sommer SS, Sobell JL, Heston LL. Sommer SS, et al. Among authors: sobell jl. Hum Genet. 1993 Dec;92(6):633-4. doi: 10.1007/BF00420955. Hum Genet. 1993. PMID: 8262527 No abstract available.

4

Screening the monoamine oxidase B gene in 100 male patients with schizophrenia: a cluster of polymorphisms in African-Americans but lack of functionally significant sequence changes.

Sobell JL, Lind TJ, Hebrink DD, Heston LL, Sommer SS. Sobell JL, et al. Am J Med Genet. 1997 Feb 21;74(1):44-9. doi: 10.1002/(sici)1096-8628(19970221)74:1<44::aid-ajmg10>3.0.co;2-r. Am J Med Genet. 1997. PMID: 9034005

5

Direct sequencing of the dopamine D2 receptor (DRD2) in schizophrenics reveals three polymorphisms but no structural change in the receptor.

Sarkar G, Kapelner S, Grandy DK, Marchionni M, Civelli O, Sobell J, Heston L, Sommer SS. Sarkar G, et al. Among authors: sobell j. Genomics. 1991 Sep;11(1):8-14. doi: 10.1016/0888-7543(91)90096-w. Genomics. 1991. PMID: 1837284

6

From molecular variant to disease: initial steps in evaluating the association of transthyretin M119 with disease.

Ii S, Sobell JL, Sommer SS. Ii S, et al. Among authors: sobell jl. Am J Hum Genet. 1992 Jan;50(1):29-41. Am J Hum Genet. 1992. PMID: 1729893 Free PMC article.

7

Delineation of genetic predisposition to multifactorial disease: a general approach on the threshold of feasibility.

Sobell JL, Heston LL, Sommer SS. Sobell JL, et al. Genomics. 1992 Jan;12(1):1-6. doi: 10.1016/0888-7543(92)90398-c. Genomics. 1992. PMID: 1733846 Review. No abstract available.

8

A novel method for detecting point mutations or polymorphisms and its application to population screening for carriers of phenylketonuria.

Sommer SS, Cassady JD, Sobell JL, Bottema CD. Sommer SS, et al. Among authors: sobell jl. Mayo Clin Proc. 1989 Nov;64(11):1361-72. doi: 10.1016/s0025-6196(12)65378-6. Mayo Clin Proc. 1989. PMID: 2687596 Review.

9

Screening the dopamine D1 receptor gene in 131 schizophrenics and eight alcoholics: identification of polymorphisms but lack of functionally significant sequence changes.

Liu Q, Sobell JL, Heston LL, Sommer SS. Liu Q, et al. Among authors: sobell jl. Am J Med Genet. 1995 Apr 24;60(2):165-71. doi: 10.1002/ajmg.1320600216. Am J Med Genet. 1995. PMID: 7485254

10

The D5 dopamine receptor gene in schizophrenia: identification of a nonsense change and multiple missense changes but lack of association with disease.

Sobell JL, Lind TJ, Sigurdson DC, Zald DH, Snitz BE, Grove WM, Heston LL, Sommer SS. Sobell JL, et al. Hum Mol Genet. 1995 Apr;4(4):507-14. doi: 10.1093/hmg/4.4.507. Hum Mol Genet. 1995. PMID: 7633397

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