Results
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Neuregulin 1 (8p12) and childhood-onset schizophrenia: susceptibility haplotypes for diagnosis and brain developmental trajectories. [electronic resource] by
- Addington, A M
- Gornick, M C
- Shaw, P
- Seal, J
- Gogtay, N
- Greenstein, D
- Clasen, L
- Coffey, M
- Gochman, P
- Long, R
- Rapoport, J L
Producer: 20070327
In:
Molecular psychiatry vol. 12
Availability: No items available.
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5.
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Sex chromosome anomalies in childhood onset schizophrenia: an update. [electronic resource] by
- Eckstrand, K
- Addington, A M
- Stromberg, T
- Merriman, B
- Miller, R
- Gochman, P
- Long, R
- Dutra, A
- Chen, Z
- Meltzer, P
- Nelson, S F
- Rapoport, J L
Producer: 20090408
In:
Molecular psychiatry vol. 13
Availability: No items available.
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Multilocus linkage analysis of the German asthma data. [electronic resource] by
- Zandi, P P
- Klein, A P
- Addington, A M
- Hetmanski, J B
- Roberts, L
- Peila, R
- Shrestha, S
- Shaw, C K
- Kiat, H C
- Langefeld, C D
- Beaty, T H
Producer: 20020415
In:
Genetic epidemiology vol. 21 Suppl 1
Availability: No items available.
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7.
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Dysbindin (DTNBP1, 6p22.3) is associated with childhood-onset psychosis and endophenotypes measured by the Premorbid Adjustment Scale (PAS). [electronic resource] by
- Gornick, M C
- Addington, A M
- Sporn, A
- Gogtay, N
- Greenstein, D
- Lenane, M
- Gochman, P
- Ordonez, A
- Balkissoon, R
- Vakkalanka, R
- Weinberger, D R
- Rapoport, J L
- Straub, R E
Producer: 20060425
In:
Journal of autism and developmental disorders vol. 35
Availability: No items available.
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A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders. [electronic resource] by
- Addington, A M
- Gauthier, J
- Piton, A
- Hamdan, F F
- Raymond, A
- Gogtay, N
- Miller, R
- Tossell, J
- Bakalar, J
- Inoff-Germain, G
- Germain, G
- Gochman, P
- Long, R
- Rapoport, J L
- Rouleau, G A
Producer: 20110603
In:
Molecular psychiatry vol. 16
Availability: No items available.
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GAD1 (2q31.1), which encodes glutamic acid decarboxylase (GAD67), is associated with childhood-onset schizophrenia and cortical gray matter volume loss. [electronic resource] by
- Addington, A M
- Gornick, M
- Duckworth, J
- Sporn, A
- Gogtay, N
- Bobb, A
- Greenstein, D
- Lenane, M
- Gochman, P
- Baker, N
- Balkissoon, R
- Vakkalanka, R K
- Weinberger, D R
- Rapoport, J L
- Straub, R E
Producer: 20050727
In:
Molecular psychiatry vol. 10
Availability: No items available.
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10.
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Segmental uniparental isodisomy on 5q32-qter in a patient with childhood-onset schizophrenia. [electronic resource] by
- Seal, J L
- Gornick, M C
- Gogtay, N
- Shaw, P
- Greenstein, D K
- Coffey, M
- Gochman, P A
- Stromberg, T
- Chen, Z
- Merriman, B
- Nelson, S F
- Brooks, J
- Arepalli, S
- Wavrant-De Vrièze, F
- Hardy, J
- Rapoport, J L
- Addington, A M
Producer: 20061215
In:
Journal of medical genetics vol. 43
Availability: No items available.
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11.
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Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disability. [electronic resource] by
- Nguyen, L S
- Jolly, L
- Shoubridge, C
- Chan, W K
- Huang, L
- Laumonnier, F
- Raynaud, M
- Hackett, A
- Field, M
- Rodriguez, J
- Srivastava, A K
- Lee, Y
- Long, R
- Addington, A M
- Rapoport, J L
- Suren, S
- Hahn, C N
- Gamble, J
- Wilkinson, M F
- Corbett, M A
- Gecz, J
Producer: 20130423
In:
Molecular psychiatry vol. 17
Availability: No items available.
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12.
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Genome-wide scan of bipolar disorder in 65 pedigrees: supportive evidence for linkage at 8q24, 18q22, 4q32, 2p12, and 13q12. [electronic resource] by
- McInnis, M G
- Lan, T-H
- Willour, V L
- McMahon, F J
- Simpson, S G
- Addington, A M
- MacKinnon, D F
- Potash, J B
- Mahoney, A T
- Chellis, J
- Huo, Y
- Swift-Scanlan, T
- Chen, H
- Koskela, R
- Stine, O Colin
- Jamison, K R
- Holmans, P
- Folstein, S E
- Ranade, K
- Friddle, C
- Botstein, D
- Marr, T
- Beaty, T H
- Zandi, P
- DePaulo, J Raymond
Producer: 20031104
In:
Molecular psychiatry vol. 8
Availability: No items available.
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