| BIBLIOGRAFIA
1. Aita VM, Liu J, Knowles JA,
Terwilliger JD, Baltazar R, Grunn A, Loth JE, Kanyas K, Lerer B, Endicott J, Wang Z,
Penchaszadeh G, Gilliam TC, Baron M. A comprehensive linkage analysis of chromosome 21q22
supports prior evidence for a putative bipolar affective disorder locus. Am J Hum Genet
1999; 64: 210-217.
2. Brzustowicz LM, Hodgkinson KA, Chow EWC, Honer WG, Bassett AS. Location of a major
susceptibility locus for familial schizophrenia on chromosome 1q21-q22. Science 2000;288:
678-682.
3. Brzustowicz LM, Honer WG, Chow EWC, Hogan J, Hodgkinson K, Bassett AS. Use of a
quantitative trait to map a locus associated with severity of positive symptoms in
familial schizophrenia to chromosome 6p. Am J Hum Genet 1997; 61: 1388-1396.
4. Brzustowicz LM, Honer WG, Chow EW, Little D, Hogan J, Hodgkinson K, Bassett AS. Linkage
of familial schizophrenia to chromosome 13q32. Am J Hum Genet 1999; 65: 1096-1103.
5. Cannon TD, Huttunen MO, Lonnqvist J, Tuulio-Henriksson A, Pirkola T, Glahn D,
Finkelstein J, Hietanen M, Kaprio J, Koskenvuo M. The Inheritance of Neuropsychological
Dysfunction in Twins Discordant for Schizophrenia. Am J Hum Genet 2000; 67:369-382.
6. Carlson C, Papolos D, Pandita RK, Faedda GL, Veit S, Goldberg R, Shprintzen R,
Kucherlapati R, Morrow B. Molecular analysis of velo-cardio-facial syndrome patients with
psychiatric disorders. Am J Hum Genet 1997; 60: 851-859.
7. Cook EH, Stein MA, Krasowski MD, Cox NJ, Olkon DM, Kieffer JE, Leventhal BL.
Association of attention-deficit disorder and the dopamine transporter gene. Am J Hum
Genet 1995; 56: 993-998.
8. Daniels JK, Spurlock G, Williams NM, Cardno AG, Jones LA, Murphy KC, Asherson P,
Holmans P, Fenton I, McGuffin P, Owen MJ. Linkage study of chromosome 6p in sib-pairs with
schizophrenia. Am J Med Genet 1997; 74: 319-323.
9. Eisenberg J, Zohar A, Mei-Tal G, Steinberg A, Tartakovsky E, Gritsenko I, Nemanov L,
Ebstein RP. A haplotype relative risk study of the dopamine D4 receptor (DRD4) exon Ill
repeat polymorphism and attention deficit hyperactivity disorder (ADHD). Am J Med Genet
2000; 96: 258-261.
10. Garner C, Kelly M, Cardon L, Joslyn G, Carey A. LeDuc C, Lichter J, Harris T, Loftus
J, Shields G, Comazzi M, Vita A, Smith AM, Dann J, Crow TJ, DeLisi LE. Linkage analyses of
schizophrenia to chromosome 6p24-p22: an attempt to replicate. Am J Med Genet 1996; 67:
595-610.
11. Kaufmann CA, Suarez B, Malaspina D, Pepple J, Svrakic D, Markel PD, Meyer J, Zambuto
CT, Schmitt K, Matise TC, Friedman JMH, Hampe C, Lee H, Shore D, Wynne D, Faraone SV,
Tsuang MT, Cloninger CR. NIMH genetics initiative millennium schizophrenia consortium:
linkage analysis of African-American pedigrees. Am J Med Genet 1998; 81: 282-289.
12. Kok LL, Solman RT. Velocardiofacial syndrome: learning difficulties and intervention.
J Med Genet 1995; 32: 612-618.
13. Mulcrone J, Whatley SA, Marchbanks R, Wildenauer D, Altmark D, Daoud H, Gur E, Ebstein
RP, Lerer B. Genetic linkage analysis of schizophrenia using chromosome 11q13-24 markers
in Israeli pedigrees. Am J Med Genet 1995; 60: 103-108.
14. Muramatsu T, Higuchi S, Murayama M, Matsushita S, Hayashida M. Association between
alcoholism and the dopamine D4 receptor gene. J Med Genet 1996; 33:113-115.
15. Schizophrenia Linkage Collaborative Group for Chromosomes 3, 6, and 8. Additional
support for schizophrenia linkage on chromosomes 6 and 8: a multicenter study. Am J Med
Genet 1996; 67: 580-594.
16. Schwab SG, Hallmayer J, Lerer B, Albus M, Borrmann M, Honig S, Strauss M, Segman R,
Lichtermann D, Knapp M, Trixler M, Maier W, Wildenauer DB. Support for a chromosome 18p
locus conferring susceptibility to functional psychoses in families with schizophrenia, by
association and linkage analysis. Am J Hum Genet 1998; 63: 1139-1152.
17. Shaw SH, Kelly M, Smith AB, Shields G, Hopkins PJ, Loftus J, Laval SH, Vita A, De Hert
M, Cardon LR, Crow TJ, Sherrington R, DeLisi LE. A genome-wide search for schizophrenia
susceptibility genes. Am J Med Genet 1998; 81: 364-376.
18. Spurlock G, Williams J, McGuffin P, Aschauer HN, Lenzinger E, Fuchs K, Sieghart WC,
Meszaros K, Fathi N, Laurent C. Mallet J, Macciardi F, Pedrini S, Gill M, Hawi Z, Gibson
S, Jazin EE, Yang H-T, Adolfsson R, Pato CN. Dourado AM, Owen MJ. European Multicentre
Association Study of Schizophrenia: a study of the DRD2 ser311-to-cys and DRD3 ser9-to-gly
polymorphisms. Am J Med Genet 1998; 81: 24-28.
19. Stine OC, Xu J, Koskela R, McMahon FJ, Gschwend M, Friddle C, Clark CD, McInnis MG,
Simpson SG, Breschel TS, Vishio E, Riskin K, Feilotter H, Chen E, Shen S, Folstein S,
Meyers DA, Botstein D, Marr TG, De Paulo JR. Evidence for linkage of bipolar disorder to
chromosome 18 with a parent-of-origin effect. Am J Hum Genet 1995; 57: 1384-1394.
20. Stober G, Saar K, Ruschendorf F, Meyer J, Nurnberg G, Jatzke S, Franzek E, Reis A,
Lesch KP, Wienker TF, Beckmann H. Splitting schizophrenia: periodic
catatonia-susceptibility locus on chromosome 15q15. Am J Hum Genet 2000; 67: 1201-1207.
21. Tomitaka M, Tomitaka S, Otuka Y, Kim K, Matuki H, Sakamoto K, Tanaka A. Association
between novelty seeking and dopamine receptor D4 (DRD4) exon III polymorphism in Japanese
subjects. Am J Med Genet 1999; 88: 469-471.
22. Yan W, Jacobsen LK, Krasnewich DM, Guan X-Y, Lenane MC, Paul SP, Dalwadi HN, Zhang H,
Long RT, Kumra S, Martin BM, Scambler PJ, Trent JM, Sidransky E, Ginns EI, Rapoport JL.
Chromosome 21q11.2 interstitial deletions among childhood-onset schizophrenics and
'multidimensionally impaired.' Am J Med Genet 1998; 81: 41-43.
Volver al Artículo
|
