-
3
-
-
0022470364
-
The family history approach to diagnosis: How useful is it?
-
Andreasen NC, Rice J, Endicott J, Reich T, Coryell W (1986), The family history approach to diagnosis: how useful is it? Arch Gen Psychiatry 43:421-429
-
(1986)
Arch Gen Psychiatry
, vol.43
, pp. 421-429
-
-
Andreasen, N.C.1
Rice, J.2
Endicott, J.3
Reich, T.4
Coryell, W.5
-
4
-
-
0026783363
-
Chromosomal aberrations and schizophrenia: Autosomes
-
Bassett AS (1992), Chromosomal aberrations and schizophrenia: autosomes. Br J Psychiatry 161:323-334
-
(1992)
Br J Psychiatry
, vol.161
, pp. 323-334
-
-
Bassett, A.S.1
-
5
-
-
0005445422
-
Psychiatric phenotype of a genetic subtype of schizophrenia
-
Bassett AS, Chow E, Scutt L, Hodgkinson K, Weksberg R (1999), Psychiatric phenotype of a genetic subtype of schizophrenia (abstract). Schizophr Res 36:87
-
(1999)
Schizophr Res
, vol.36
, pp. 87
-
-
Bassett, A.S.1
Chow, E.2
Scutt, L.3
Hodgkinson, K.4
Weksberg, R.5
-
6
-
-
0030828882
-
Enlarged Sylvian fissures in infants with interstitial deletion of chromosome 22q11
-
Bingham PM, Zimmerman RA, McDonald-McGinn D, Driscoll D, Emanuel BS, Zackai E (1997), Enlarged Sylvian fissures in infants with interstitial deletion of chromosome 22q11. Am J Med Genet 74:538-543
-
(1997)
Am J Med Genet
, vol.74
, pp. 538-543
-
-
Bingham, P.M.1
Zimmerman, R.A.2
McDonald-McGinn, D.3
Driscoll, D.4
Emanuel, B.S.5
Zackai, E.6
-
7
-
-
0022686607
-
Age at onset and causes of disease
-
Childs B, Scriver CR (1986), Age at onset and causes of disease. Perspect Biol Med 29:437-460
-
(1986)
Perspect Biol Med
, vol.29
, pp. 437-460
-
-
Childs, B.1
Scriver, C.R.2
-
8
-
-
0003000204
-
MRI findings in adults with 22q11 deletion syndrome (22qDS) and schizophrenia
-
Chow E, Zipursky RB, Mikulis D, Scutt L, Weksberg R, Bassett AS (1999), MRI findings in adults with 22q11 deletion syndrome (22qDS) and schizophrenia (abstract). Schizophr Res 36:89
-
(1999)
Schizophr Res
, vol.36
, pp. 89
-
-
Chow, E.1
Zipursky, R.B.2
Mikulis, D.3
Scutt, L.4
Weksberg, R.5
Bassett, A.S.6
-
9
-
-
0028305380
-
Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease
-
Corder EH, Saunders AM, Risch NJ et al. (1994), Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease. Nat Genet 7:180-184
-
(1994)
Nat Genet
, vol.7
, pp. 180-184
-
-
Corder, E.H.1
Saunders, A.M.2
Risch, N.J.3
-
10
-
-
0031578929
-
Is schizophrenia the price that Homo sapiens pays for language?
-
Crow TJ (1997), Is schizophrenia the price that Homo sapiens pays for language? Schizophr Res 28:127-141
-
(1997)
Schizophr Res
, vol.28
, pp. 127-141
-
-
Crow, T.J.1
-
12
-
-
8944227512
-
Brain anatomic magnetic resonance imaging in childhood-onset schizophrenia
-
Frazier JA, Giedd JN, Hamburger SD et al. (1996), Brain anatomic magnetic resonance imaging in childhood-onset schizophrenia. Arch Gen Psychiatry 53:617-624
-
(1996)
Arch Gen Psychiatry
, vol.53
, pp. 617-624
-
-
Frazier, J.A.1
Giedd, J.N.2
Hamburger, S.D.3
-
13
-
-
0003604142
-
-
New York: Anxiety Disorders Clinic, New York State Psychiatric Institute
-
Fyer AJ, Endicott J, Mannuzza S, Klein DF (1985), Schedule for Affective Disorders and Schizophrenia-Lifetime Anxiety Version (SADS-LA). New York: Anxiety Disorders Clinic, New York State Psychiatric Institute
-
(1985)
Schedule for Affective Disorders and Schizophrenia-Lifetime Anxiety Version (SADS-LA)
-
-
Fyer, A.J.1
Endicott, J.2
Mannuzza, S.3
Klein, D.F.4
-
14
-
-
0001898509
-
Anatomic basis of cerebral dominance
-
Davidson RJ, Hugdahl K, eds. Cambridge, MA: MIT Press
-
Galaburda AM (1995), Anatomic basis of cerebral dominance. In: Brain Asymmetry, Davidson RJ, Hugdahl K, eds. Cambridge, MA: MIT Press, pp 51-73
-
(1995)
Brain Asymmetry
, pp. 51-73
-
-
Galaburda, A.M.1
-
15
-
-
13044317285
-
A genome-wide search for chromosomal loci linked to mental health wellness in relatives at high risk for bipolar affective disorder among the Old Order Amish
-
Ginns EI, St Jean P, Philibert RA et al. (1998), A genome-wide search for chromosomal loci linked to mental health wellness in relatives at high risk for bipolar affective disorder among the Old Order Amish. Proc Natl Acad Sci U S A 95:15531-15536
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, pp. 15531-15536
-
-
Ginns, E.I.1
St Jean, P.2
Philibert, R.A.3
-
17
-
-
0028125305
-
Childhood-onset schizophrenia: An NIMH study in progress
-
Gordon CT, Frazier JA, McKenna K et al. (1994), Childhood-onset schizophrenia: an NIMH study in progress. Schizophr Bull 20:697-712
-
(1994)
Schizophr Bull
, vol.20
, pp. 697-712
-
-
Gordon, C.T.1
Frazier, J.A.2
McKenna, K.3
-
19
-
-
0028937677
-
Child and adolescent (juvenile onset) schizophrenia: A case control study of prcmorbid developmental impairments
-
Hollis C (1995), Child and adolescent (juvenile onset) schizophrenia: a case control study of prcmorbid developmental impairments. Br J Psychiatry 166:489-495
-
(1995)
Br J Psychiatry
, vol.166
, pp. 489-495
-
-
Hollis, C.1
-
20
-
-
0031557106
-
Quantitative magnetic resonance imaging of the corpus callosum in childhood onset schizophrenia
-
Jacobsen LK, Giedd JN, Rajapakse JC et al. (1997), Quantitative magnetic resonance imaging of the corpus callosum in childhood onset schizophrenia. Psychiatry Res 68:77-86
-
(1997)
Psychiatry Res
, vol.68
, pp. 77-86
-
-
Jacobsen, L.K.1
Giedd, J.N.2
Rajapakse, J.C.3
-
21
-
-
0031974891
-
Research update: Childhood-onset schizophrenia: implications of clinical and neurobiological research
-
Jacobsen LK, Rapoport JL (1998), Research update: childhood-onset schizophrenia: implications of clinical and neurobiological research. J Child Psychol Psychiatry 39:101-113
-
(1998)
J Child Psychol Psychiatry
, vol.39
, pp. 101-113
-
-
Jacobsen, L.K.1
Rapoport, J.L.2
-
22
-
-
0030813634
-
A turning point in schizophrenia genetics
-
Karayiorgou M, Gogos JA (1997), A turning point in schizophrenia genetics. Neuron 19:967-979
-
(1997)
Neuron
, vol.19
, pp. 967-979
-
-
Karayiorgou, M.1
Gogos, J.A.2
-
23
-
-
0029102665
-
Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11
-
Karayiorgou M, Morris MA, Morrow B et al. (1995), Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11. Proc Natl Acad Sci USA 92:7612-7616
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 7612-7616
-
-
Karayiorgou, M.1
Morris, M.A.2
Morrow, B.3
-
24
-
-
0030954243
-
Schedule for Affective Disorders and Schizophrenia for School-Age Children-Present and Lifetime Version (K-SADS-PL): Initial reliability and validity data
-
Kaufman J, Birmaher B, Brent D et al. (1997), Schedule for Affective Disorders and Schizophrenia for School-Age Children-Present and Lifetime Version (K-SADS-PL): initial reliability and validity data. J Am Acad Child Adolesc Psychiatry 36:980-988
-
(1997)
J Am Acad Child Adolesc Psychiatry
, vol.36
, pp. 980-988
-
-
Kaufman, J.1
Birmaher, B.2
Brent, D.3
-
25
-
-
0027459424
-
Confirmation that the velocardio-facial syndrome is associated with halpo-insufficiency of genes at chromosome 22q11
-
Kelly D, Goldberg R, Wilson D et al. (1993), Confirmation that the velocardio-facial syndrome is associated with halpo-insufficiency of genes at chromosome 22q11. Am J Med Genet 45:308-312
-
(1993)
Am J Med Genet
, vol.45
, pp. 308-312
-
-
Kelly, D.1
Goldberg, R.2
Wilson, D.3
-
26
-
-
0031937498
-
Brief report: Association of sex chromosome anomalies with childhood-onset psychotic disorders
-
Kumra S, Wiggs E, Krasnewich D et al. (1998), Brief report: association of sex chromosome anomalies with childhood-onset psychotic disorders. J Am Acad Child Adolesc Psychiatry 37:292-296
-
(1998)
J Am Acad Child Adolesc Psychiatry
, vol.37
, pp. 292-296
-
-
Kumra, S.1
Wiggs, E.2
Krasnewich, D.3
-
27
-
-
0031932403
-
Brain abnormality in schizophrenia: A systematic and quantitative review of volumetric magnetic resonance imaging studies
-
Lawrie SM, Abukmeil SS (1998), Brain abnormality in schizophrenia: a systematic and quantitative review of volumetric magnetic resonance imaging studies. Br J Psychiatry 172:110-120
-
(1998)
Br J Psychiatry
, vol.172
, pp. 110-120
-
-
Lawrie, S.M.1
Abukmeil, S.S.2
-
28
-
-
0024546495
-
Precise localization of NF1 to 17q11.2 by balanced translocation
-
Ledbetter DH, Rich DC, O'Connell P, Leppert M, Carey JC (1989), Precise localization of NF1 to 17q11.2 by balanced translocation. Am J Hum Genet 44:20-24
-
(1989)
Am J Hum Genet
, vol.44
, pp. 20-24
-
-
Ledbetter, D.H.1
Rich, D.C.2
O'Connell, P.3
Leppert, M.4
Carey, J.C.5
-
29
-
-
0029166983
-
Cerebellar atrophy in a patient with velocardiofacial syndrome
-
Lynch DR, McDonald-McGinn DM, Zackai EH et al. (1995), Cerebellar atrophy in a patient with velocardiofacial syndrome. J Med Genet 32:561-563
-
(1995)
J Med Genet
, vol.32
, pp. 561-563
-
-
Lynch, D.R.1
McDonald-McGinn, D.M.2
Zackai, E.H.3
-
31
-
-
0028290436
-
Looking for childhood-onset schizophrenia: The first 71 cases screened
-
McKenna K, Gordon CT, Lenane M, Kaysen D, Fahey K, Rapoport JL (1994), Looking for childhood-onset schizophrenia: the first 71 cases screened. J Am Acad Child Adolesc Psychiatry 33:636-644
-
(1994)
J Am Acad Child Adolesc Psychiatry
, vol.33
, pp. 636-644
-
-
McKenna, K.1
Gordon, C.T.2
Lenane, M.3
Kaysen, D.4
Fahey, K.5
Rapoport, J.L.6
-
33
-
-
13044292229
-
The behavioural phenotype in velo-cardiofacial syndrome
-
Murphy KC, Owen MJ (1998), The behavioural phenotype in velo-cardiofacial syndrome. J Med Genet 35:517
-
(1998)
J Med Genet
, vol.35
, pp. 517
-
-
Murphy, K.C.1
Owen, M.J.2
-
34
-
-
0023638471
-
Is schizophrenia a neurodevelopmental disorder?
-
Murray RM, Lewis SW (1987), Is schizophrenia a neurodevelopmental disorder? Br Med J 295:681-682
-
(1987)
Br Med J
, vol.295
, pp. 681-682
-
-
Murray, R.M.1
Lewis, S.W.2
-
35
-
-
84920323243
-
Childhood-onset schizophrenia: What can it teach us?
-
in press, Rapoport JL, ed. Washington, DC: American Psychiatric Press
-
Nicolson R, Rapoport JL (in press), Childhood-onset schizophrenia: what can it teach us? In: Childhood Onset of "Adult" Psychopathology: Clinical and Research Advances, Rapoport JL, ed. Washington, DC: American Psychiatric Press
-
Childhood Onset of "Adult" Psychopathology: Clinical and Research Advances
-
-
Nicolson, R.1
Rapoport, J.L.2
-
36
-
-
0040920369
-
-
Johns Hopkins University, Baltimore. MIM number: 188400
-
Online Mendelian Inheritance in Man, OMIM[TRADE] (1999), Johns Hopkins University, Baltimore. MIM number: 188400; World Wide Web URL: http://www.ncbi.nlm.nih.gov/omim
-
(1999)
Online Mendelian Inheritance in Man, OMIM[TRADE]
-
-
-
37
-
-
0015218436
-
The topographical distribution of interhemispheric projections in the corpus callosum of the rhesus monkey
-
Pandya DN, Karol EA, Heilbronn D (1971),The topographical distribution of interhemispheric projections in the corpus callosum of the rhesus monkey. Brain Res 32:31-43
-
(1971)
Brain Res
, vol.32
, pp. 31-43
-
-
Pandya, D.N.1
Karol, E.A.2
Heilbronn, D.3
-
38
-
-
0029853761
-
Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: Does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder?
-
Papolos DF, Faedda GL, Veit S et al. (1996), Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder? Am J Psychiatry 153:1541-1547
-
(1996)
Am J Psychiatry
, vol.153
, pp. 1541-1547
-
-
Papolos, D.F.1
Faedda, G.L.2
Veit, S.3
-
40
-
-
0030763042
-
Chemokine receptor CCR5 genotype influences the kinetics of human immunodeficiency virus type 1 infection in human PBL-SCID mice
-
Picchio GR, Gulizia RJ, Mosier DE (1997), Chemokine receptor CCR5 genotype influences the kinetics of human immunodeficiency virus type 1 infection in human PBL-SCID mice. J Virol 71:7124-7127
-
(1997)
J Virol
, vol.71
, pp. 7124-7127
-
-
Picchio, G.R.1
Gulizia, R.J.2
Mosier, D.E.3
-
41
-
-
0027989917
-
Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives
-
Pulver AE, Nestadt G, Goldberg R et al. (1994), Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives. J Nerv Ment Dis 182:476-478
-
(1994)
J Nerv Ment Dis
, vol.182
, pp. 476-478
-
-
Pulver, A.E.1
Nestadt, G.2
Goldberg, R.3
-
42
-
-
0022347518
-
Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophy
-
Ray PN, Belfall B, Duff C et al. (1985), Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophy. Nature 318:672-675
-
(1985)
Nature
, vol.318
, pp. 672-675
-
-
Ray, P.N.1
Belfall, B.2
Duff, C.3
-
43
-
-
0025019555
-
Linkage strategies for genetically complex traits, I: Multilocus models
-
Risch N (1990), Linkage strategies for genetically complex traits, I: multilocus models. Am J Hum Genet 46:222-228
-
(1990)
Am J Hum Genet
, vol.46
, pp. 222-228
-
-
Risch, N.1
-
44
-
-
16944364802
-
Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: A European collaborative study
-
Ryan AK, Goodship JA, Wilson DI et al. (1997), Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study. J Med Genet 34:798-804
-
(1997)
J Med Genet
, vol.34
, pp. 798-804
-
-
Ryan, A.K.1
Goodship, J.A.2
Wilson, D.I.3
-
45
-
-
0029783493
-
Prevalence of 22q11 microdeletion
-
Tezenas Du Montcel S, Mendizabai H, Ayme S, Levy A, Philip N (1996), Prevalence of 22q11 microdeletion. J Med Genet 33:719
-
(1996)
J Med Genet
, vol.33
, pp. 719
-
-
Tezenas Du Montcel, S.1
Mendizabai, H.2
Ayme, S.3
Levy, A.4
Philip, N.5
-
46
-
-
0028858104
-
The case for heterogeneity in the etiology of schizophrenia
-
Tsuang MT, Faraone SV (1995), The case for heterogeneity in the etiology of schizophrenia. Schizophr Res 17:161-175
-
(1995)
Schizophr Res
, vol.17
, pp. 161-175
-
-
Tsuang, M.T.1
Faraone, S.V.2
-
47
-
-
0000179688
-
A human genetic model for schizophrenia: Brain structure and function of people with velocardio-facial syndrome
-
van Amelsvoort T, Daly E, Critchley H et al. (1999), A human genetic model for schizophrenia: brain structure and function of people with velocardio-facial syndrome (abstract). Schizophr Res 36:213
-
(1999)
Schizophr Res
, vol.36
, pp. 213
-
-
Van Amelsvoort, T.1
Daly, E.2
Critchley, H.3
-
49
-
-
0023215296
-
Implications of normal brain development for the pathogenesis of schizophrenia
-
Weinberger DR (1987), Implications of normal brain development for the pathogenesis of schizophrenia. Arch Gen Psychiatry 44:660-669
-
(1987)
Arch Gen Psychiatry
, vol.44
, pp. 660-669
-
-
Weinberger, D.R.1
-
50
-
-
0007482654
-
Chromosome 22q11.2 interstitial deletions among childhood-onset schizophrenics and "multidimensionally impaired."
-
Van W, Jacobsen LK, Krasnewich DM et al. (1998), Chromosome 22q11.2 interstitial deletions among childhood-onset schizophrenics and "multidimensionally impaired." Am J Med Genet 81:41-43
-
(1998)
Am J Med Genet
, vol.81
, pp. 41-43
-
-
Van, W.1
Jacobsen, L.K.2
Krasnewich, D.M.3
|