A compelling genetic hypothesis for a complex disease:: PRODH2/DGCR6 variation leads to schizophrenia susceptibility

被引:28
作者
Chakravarti, A [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, McKusick Nathans Inst Genet Med, Baltimore, MD 21287 USA
关键词
D O I
10.1073/pnas.092158299
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
引用
收藏
页码:4755 / 4756
页数:2
相关论文
共 14 条
[1]   Human-specific duplication and mosaic transcripts: The recent paralogous structure of chromosome 22 [J].
Bailey, JA ;
Yavor, AM ;
Viggiano, L ;
Misceo, D ;
Horvath, JE ;
Archidiacono, N ;
Schwartz, S ;
Rocchi, M ;
Eichler, EE .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 70 (01) :83-100
[2]   Genetics of schizophrenia and the new millennium: Progress and pitfalls [J].
Baron, M .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 68 (02) :299-312
[3]   Population genetics - making sense out of sequence [J].
Chakravarti, A .
NATURE GENETICS, 1999, 21 (Suppl 1) :56-60
[4]   The DNA sequence of human chromosome 22 [J].
Dunham, I ;
Shimizu, N ;
Roe, BA ;
Chissoe, S ;
Dunham, I ;
Hunt, AR ;
Collins, JE ;
Bruskiewich, R ;
Beare, DM ;
Clamp, M ;
Smink, LJ ;
Ainscough, R ;
Almeida, JP ;
Babbage, A ;
Bagguley, C ;
Balley, J ;
Barlow, K ;
Bates, KN ;
Beasley, O ;
Bird, CP ;
Blakey, S ;
Bridgeman, AM ;
Buck, D ;
Burgess, J ;
Burrill, WD ;
Burton, J ;
Carder, C ;
Carter, NP ;
Chen, Y ;
Clark, G ;
Clegg, SM ;
Cobley, V ;
Cole, CG ;
Collier, RE ;
Connor, RE ;
Conroy, D ;
Corby, N ;
Coville, GJ ;
Cox, AV ;
Davis, J ;
Dawson, E ;
Dhami, PD ;
Dockree, C ;
Dodsworth, SJ ;
Durbin, RM ;
Ellington, A ;
Evans, KL ;
Fey, JM ;
Fleming, K ;
French, L .
NATURE, 1999, 402 (6761) :489-495
[5]   The gene encoding proline dehydrogenase modulates sensorimotor gating in mice [J].
Gogos, JA ;
Santha, M ;
Takacs, Z ;
Beck, KD ;
Luine, V ;
Lucas, LR ;
Nadler, JV ;
Karayiorgou, M .
NATURE GENETICS, 1999, 21 (04) :434-439
[6]   Hyperprolinaemia in patients with deletion (22)(q11.2) syndrome [J].
Goodman, BK ;
Rutberg, J ;
Lin, WW ;
Pulver, AE ;
Thomas, GH ;
Geraghty, MT .
JOURNAL OF INHERITED METABOLIC DISEASE, 2000, 23 (08) :847-848
[7]  
JIMINEZSANCHEZ J, 2001, NATURE, V409, P853
[8]   Understanding the molecular basis of fragile X syndrome [J].
Jin, P ;
Warren, ST .
HUMAN MOLECULAR GENETICS, 2000, 9 (06) :901-908
[9]   SCHIZOPHRENIA SUSCEPTIBILITY ASSOCIATED WITH INTERSTITIAL DELETIONS OF CHROMOSOME 22Q11 [J].
KARAYIORGOU, P ;
MORRIS, MA ;
MORROW, B ;
SHPRINTZEN, RJ ;
GOLDBERG, R ;
BORROW, J ;
GOS, A ;
NESTADT, G ;
WOLYNIEC, PS ;
LASSETER, VK ;
EISEN, H ;
CHILDS, B ;
KAZAZIAN, HH ;
KUCHERLAPATI, R ;
ANTONARAKIS, SE ;
PULVER, AE ;
HOUSMAN, DE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (17) :7612-7616
[10]   GENETIC DISSECTION OF COMPLEX TRAITS [J].
LANDER, ES ;
SCHORK, NJ .
SCIENCE, 1994, 265 (5181) :2037-2048