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Schizophrenia

Schizophrenia 20.21

Distribution 20.21 of the NIMH Schizophrenia Genetics Initiative contains a total of 54,787 individuals from 22,254 families (37,766 individuals have DNA cell lines available; 17,429 individuals have plasma available). 53,637 individuals in 21,576 families were in the previous distribution (Distribution 19.0). New in this collection: Study 92 – 32 individuals from 32 families (32 subjects with cell lines and 29 subjects with plasma), Study 122 – 325 individuals from one family (215 subjects with cell lines and 209 subjects with plasma), Updated Study 76 – 10,069 individuals from 8,940 families (9,784 subjects with cell lines and 5,671 subjects with plasma). Note: 9,276 subjects in version 19.0 were replaced by 10,069 subjects in version 20.0.

Standard Data & Documentation

  • Distribution Bundle [ or ]: Standard files across disorders, containing demographic, diagnostic, and pedigree information. RUCDR sample IDs (cell_id) and consent level are also provided. Bundle includes data dictionaries and change notes.
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Additional Data Files

Genetic Data

Full Genome Genotyping

  • Genome-wide Pedigree Data, December 2012, n=1534 pedigrees.
  • For more information, visit the CAPS homepage.
  • SNP Genotypes for Select Pedigrees, April 2014, n=47 pedigrees, 330 subjects. Affymetrix Axiom Lat platform. .CEL files must be shipped due to the large size of the files. To request shipment, please contact help@nrgr.on.spiceworks.com and reference your active access approval ID.
  • For more information, visit the CAPS homepage.

Genetic Data

Full Genome Genotyping

Genetic Data

Full Genome Genotyping

  • Full genome screen, 12,015 markers. 1,546 subjects. Data is provided by Anna Need from multiple studies: Study 0 (123 subjects), Study 12 (69 subjects), Study 15 (42 subjects), Study 22 (549 subjects), Study 23 (119 subjects), Study 29 (207 subjects), and Study 6 (398 subjects).  There are 39 subjects in Dr. Anna Need's genotype file but are not included in Schizophrenia Dist. 9.0.

Genetic Data

Full Genome Genotyping

  • 7,584 markers on chr 1-22. 639 subjects. Data is provided by Dr. Mark Brennan from multiple studies.  It includes 424 subjects from CATIE (study 17) and 215 subjects from GAIN.

Genetic Data

Sequence - Targeted Gene

  • Next Generation Sequencing of Two Genes on chr 8 (EGR3 and ARC), 4,066 subjects. This data is available by request due to the large size of the files.  To request shipment, please contact help@nrgr.on.spiceworks.com and reference your active access approval ID.

Targeted Genotyping

  • 14 Genes, 648 SNPs Markers. 1870 cases, 2002 controls. Subjects from multiple studies (NIMH SZ study 0, study 6, study 29).

Genetic Data

Targeted Genotyping

  • 240 SNPs, 42 genes, on Chromosomes 1-6, 8-13, 22, X, Y. 761 subjects from multiple studies (NIMH SZ study 0, study 6, study 12).

Genetic Data

Full Genome Genotyping

  • 375 Markers on Chromosome 1 to Chromosome 22, 15 Markers on Chromosome X. 2,405 subjects.

Targeted Genotyping

  • PLXNA2 Gene, 3 Microsatellite Markers and 4 SNPs Markers on Chromosome 1. 1,143 subjects.
Clinical Instruments

DIGS

Diagnostic Interview for Genetic Studies (DIGS) - The CSV-format DIGS interview files provided below are cleaned versions of those received from the original study investigators. While they retain the record layouts and variable naming of their respective DIGS versions, they have had invalid values corrected or removed, date fields converted to a standard format, and their various missing/ unknown values converted to standard textual metavalues in order to avoid misinterpretation. Further details on the cleaning that has been performed are included in the file "sz-digs-cleaning-readme.txt" included in the download. To download the original files as received from study investigators, use "original" links below.

The DIGS data for Study 3a (Site 35) was collected by using DIGS Version 2.0.

Genetic Data

Full Genome Genotyping

  • 401 markers, STRP genotype data from Chromosome 1-23, for 1,422 African American and European American subjects
Clinical Instruments

DIGS

Diagnostic Interview for Genetic Studies (DIGS) - The CSV-format DIGS interview files provided below are cleaned versions of those received from the original study investigators. While they retain the record layouts and variable naming of their respective DIGS versions, they have had invalid values corrected or removed, date fields converted to a standard format, and their various missing/ unknown values converted to standard textual metavalues in order to avoid misinterpretation. Further details on the cleaning that has been performed are included in the file "sz-digs-cleaning-readme.txt" included in the download. To download the original files as received from study investigators, use "original" links below.

The DIGS data for Study 6 (Sites 41-49) was collected by using DIGS Version 2.1.

Genetic Data

Full Genome Genotyping

  • Full Genome Screen of 1,323 subjects, Illumina 2.5M4; 2.5M8; 550k v1, v2; 610k; 660k
Clinical Instruments

Other

Clinical Instruments

BEFD

DIGS

Diagnostic Interview for Genetic Studies (DIGS) - The CSV-format DIGS interview files provided below are cleaned versions of those received from the original study investigators. While they retain the record layouts and variable naming of their respective DIGS versions, they have had invalid values corrected or removed, date fields converted to a standard format, and their various missing/ unknown values converted to standard textual metavalues in order to avoid misinterpretation. Further details on the cleaning that has been performed are included in the file "sz-digs-cleaning-readme.txt" included in the download. To download the original files as received from study investigators, use "original" links below.

The DIGS data for Study 12 (Site 33) was collected by using DIGS Version 2.0.

Genetic Data

Full Genome Genotyping

  • Full Genome Screen - Escamilla 2003 Linkage Data. 434 subjects.
  • Full Genome Screen - Escamilla 2005 Linkage Data. 868 subjects.
Clinical Instruments

DIGS

Diagnostic Interview for Genetic Studies (DIGS) - The CSV-format DIGS interview files provided below are cleaned versions of those received from the original study investigators. While they retain the record layouts and variable naming of their respective DIGS versions, they have had invalid values corrected or removed, date fields converted to a standard format, and their various missing/ unknown values converted to standard textual metavalues in order to avoid misinterpretation. Further details on the cleaning that has been performed are included in the file "sz-digs-cleaning-readme.txt" included in the download. To download the original files as received from study investigators, use "original" links below.

The DIGS data for Study 13 (Sites 53, 54, 55, 56, 57, 58, 59) was collected by using DIGS Version 2.0 or 2.1.

Genetic Data

Full Genome Genotyping

  • Chromosomes 1-22, 386 Microsatellite Markers and 93 SNP Markers. 616 subjects.
Clinical Instruments

BEFD

DIGS

Diagnostic Interview for Genetic Studies (DIGS) - The CSV-format DIGS interview files provided below are cleaned versions of those received from the original study investigators. While they retain the record layouts and variable naming of their respective DIGS versions, they have had invalid values corrected or removed, date fields converted to a standard format, and their various missing/ unknown values converted to standard textual metavalues in order to avoid misinterpretation. Further details on the cleaning that has been performed are included in the file "sz-digs-cleaning-readme.txt" included in the download. To download the original files as received from study investigators, use "original" links below.

The DIGS data for Study 15 (Sites 70, 71) was collected by using DIGS Version 2.0.

Genetic Data

Full Genome Genotyping

  • CATIE Genome-Wide Association Data. Case-Control. PLINK files from Affymetrix 500k platform. 741 cases, 751 controls.
  • CATIE Genome-Wide Association Data, 291 cases. PLINK files from Affymetrix 6.0 platform. CEL files and CHP files are sent by request due to the large size of the files. To request shipment, please contact help@nrgr.on.spiceworks.com and reference your active access approval ID.
Clinical Instruments

BEFD

Clinical Trial

  • Clinical Antipsychotic Trials of Intervention Effectiveness data, Including SCID, family interviews, laboratory results, adverse event reports, and more.

Genetic Data

Full Genome Genotyping

  • Full Genome Screen - PAARTNERS. 5,756 markers. 787 subjects.
Clinical Instruments

Clinical Trial

DIGS

Diagnostic Interview for Genetic Studies (DIGS) - The CSV-format DIGS interview files provided below are cleaned versions of those received from the original study investigators. While they retain the record layouts and variable naming of their respective DIGS versions, they have had invalid values corrected or removed, date fields converted to a standard format, and their various missing/ unknown values converted to standard textual metavalues in order to avoid misinterpretation. Further details on the cleaning that has been performed are included in the file "sz-digs-cleaning-readme.txt" included in the download. To download the original files as received from study investigators, use "original" links below.

The DIGS data for Study 22 (Sites 101-108) was collected by using DIGS Version 3.0 and Version 4.0.

Clinical Instruments

DIGS

Diagnostic Interview for Genetic Studies (DIGS) - The CSV-format DIGS interview files provided below are cleaned versions of those received from the original study investigators. While they retain the record layouts and variable naming of their respective DIGS versions, they have had invalid values corrected or removed, date fields converted to a standard format, and their various missing/ unknown values converted to standard textual metavalues in order to avoid misinterpretation. Further details on the cleaning that has been performed are included in the file "sz-digs-cleaning-readme.txt" included in the download. To download the original files as received from study investigators, use "original" links below.

The DIGS data for Study 23 (Site 73) was collected by using DIGS Version 2.0.

Clinical Instruments

Other

  • Includes anti-saccade performance data, demographics, GAF, WRAT, and CVLT summary scores, and a number of Cognitive accuracy & speed scores.
  • Includes anti-saccade performance data, demographics, GAF, WRAT, and CVLT summary scores, and a number of Cognitive accuracy & speed scores.

Clinical Instruments

DIGS

Diagnostic Interview for Genetic Studies (DIGS) - The CSV-format DIGS interview files provided below are cleaned versions of those received from the original study investigators. While they retain the record layouts and variable naming of their respective DIGS versions, they have had invalid values corrected or removed, date fields converted to a standard format, and their various missing/ unknown values converted to standard textual metavalues in order to avoid misinterpretation. Further details on the cleaning that has been performed are included in the file "sz-digs-cleaning-readme.txt" included in the download. To download the original files as received from study investigators, use "original" links below.

The DIGS data for Study 29 (Sites 139-149) was collected by using DIGS Version 2.2.

Clinical Instruments

DIGS

Diagnostic Interview for Genetic Studies (DIGS) - The CSV-format DIGS interview files provided below are cleaned versions of those received from the original study investigators. While they retain the record layouts and variable naming of their respective DIGS versions, they have had invalid values corrected or removed, date fields converted to a standard format, and their various missing/ unknown values converted to standard textual metavalues in order to avoid misinterpretation. Further details on the cleaning that has been performed are included in the file "sz-digs-cleaning-readme.txt" included in the download. To download the original files as received from study investigators, use "original" links below.

The DIGS data for Study 42 (Site 185) was collected by using DIGS Version 3.0 Revised 7.

Other

Clinical Instruments

DIGS

Diagnostic Interview for Genetic Studies (DIGS) - The CSV-format DIGS interview files provided below are cleaned versions of those received from the original study investigators. While they retain the record layouts and variable naming of their respective DIGS versions, they have had invalid values corrected or removed, date fields converted to a standard format, and their various missing/ unknown values converted to standard textual metavalues in order to avoid misinterpretation. Further details on the cleaning that has been performed are included in the file "sz-digs-cleaning-readme.txt" included in the download. To download the original files as received from study investigators, use "original" links below.

DIGS data for study 59 is in Comprehensive Assessment of Symptoms and History (CASH) format.

Clinical Instruments

Other

  • Extended diagnosis file (DSM4 codes) and Study-provided diagnosis definitions

Clinical Instruments

Other

Clinical Instruments

Clinical Trial

  • Including demographics, physical & medical exam, SCID, BPRS, CGI, medication logs, adverse event reports, and more.

Genetic Data

Targeted Genotyping

Clinical Instruments

Other

  • Includes OPCRIT data, extended diagnosis file (DSM4), and study-defined diagnosis file.

This study does not have any additional genetic or clinical data. All study data is included in the standard distribution files above.

Clinical Instruments

Other

Genetic Data

Full Genome Genotyping

  • GWAS from Ireland, 3,878 subjects. This dataset is available by request due to the large size of the files, including an archive of genotypes, .cel files, and diagnostic clinical information for the existing samples. Please contact help@nrgr.on.spiceworks.com and reference your active access approval ID.

This study does not have any additional genetic or clinical data. All study data is included in the standard distribution files above.

Clinical Instruments

DIGS

Diagnostic Interview for Genetic Studies (DIGS) - The CSV-format DIGS interview files provided below are cleaned versions of those received from the original study investigators. While they retain the record layouts and variable naming of their respective DIGS versions, they have had invalid values corrected or removed, date fields converted to a standard format, and their various missing/ unknown values converted to standard textual metavalues in order to avoid misinterpretation. Further details on the cleaning that has been performed are included in the file "sz-digs-cleaning-readme.txt" included in the download. To download the original files as received from study investigators, use "original" links below.

DIGS data for Study 92 (Sites 320-321) were collected by using DIGS Version 2.0

Genetic Data

Sequence - Exome

  • CIAC case-control data. This dataset is available by request due to the large size of the files, including Whole-Exome Sequencing (Illumina HiSeq2000 - 443 subjects, 67 cases), Illumina HumanExome BeadChip (Exome Chip - 319 subjects, 113 cases), Illumina OmniExpress BeadChip (GWAS Chip - 384 subjects, 135 cases) data. Please contact help@nrgr.on.spiceworks.com and reference your active access approval ID.
Clinical Instruments

Other

  • Data on presence of absence of granulocytes during treatment with clozapine, for both cases and controls

Clinical Instruments

Clinical Trial

Clinical Instruments

Other

  • Study-specific diagnosis definitions and blank interview forms.

Genetic Data

Full Genome Genotyping

  • Full Genome Screen, Alternate version of SZ Dataset 8.01. 455 markers, 261 subjects.
  • Full Genome Screen. 624 markers, 109 subjects.
  • Full Genome Screen, alternate version of SZ Dataset 1.03. 455 markers, 261 subjects.

Sequence - Exome

  • Exome Sequence data (ABI SOLiDv4) on 12 family cases from sites 30 & 32, Dr. Debby Tsuang. BAM files are shipped upon request due to the large size of the files. To request shipment, please contact help@nrgr.on.spiceworks.com and reference your active access approval ID.

Targeted Genotyping

  • 13 markers on chromosome 4, 14 markers on chromosome 22, and 3 SNPs and 1 microsatellite marker in the Sult 4A region on chromosome 22. 169 subjects.
  • 5 BDNF Markers. 42 subjects.
  • 21 Markers on Chromosome 4 and 43 Markers on Chromosome 22. 225 subjects.
  • Syn2 Gene, 4 Microsatellite Markers and 11 SNPs Markers on Chromosome 3. 231 subjects.
  • Alpha2B Adrenoceptor for 26 Trios, 78 subjects.
  • 10 Markers for Chromosome 22, 429 subjects.
  • hKCa3 on Chromosome 1q21, 240 subjects.
  • 9 Markers on Chromosome 6, 371 subjects.
  • 3 Markers on Chromosome 15, 182 subjects.
  • K274E Mutation in PAH, 68 subjects.
  • Aromatic amino acid hydroxylase genes 8 markers for PAH, TPH, TH. 69 subjects.
Clinical Instruments

BEFD

DIGS

Diagnostic Interview for Genetic Studies (DIGS) - The CSV-format DIGS interview files provided below are cleaned versions of those received from the original study investigators. While they retain the record layouts and variable naming of their respective DIGS versions, they have had invalid values corrected or removed, date fields converted to a standard format, and their various missing/ unknown values converted to standard textual metavalues in order to avoid misinterpretation. Further details on the cleaning that has been performed are included in the file "sz-digs-cleaning-readme.txt" included in the download. To download the original files as received from study investigators, use "original" links below.

The DIGS data for Study 0 (Sites 30, 31, 32) was collected by using DIGS Version 1.0 or 2.0, both versions have a core of variables in common.

Genetic Data

Full Genome Genotyping

  • No samples hosted at NIMH Repository and Genomics Resource. This dataset is hosted for public download by request of Pat Sullivan. Data from multi-stage genome-wide association study (GWAS) for schizophrenia beginning with a Swedish national sample (5,001 cases and 6,243 controls) followed by meta-analysis with previous schizophrenia GWAS (8,832 cases and 12,067 controls) and finally by replication of SNPs in 168 genomic regions in independent samples (7,413 cases, 19,762 controls and 581 parent-offspring trios).

CAPS

  • Genome-wide Pedigree Data, December 2012, n=1534 pedigrees.
  • For more information, visit the CAPS homepage.
  • SNP Genotypes for Select Pedigrees, April 2014, n=47 pedigrees, 330 subjects. Affymetrix Axiom Lat platform. .CEL files must be shipped due to the large size of the files. To request shipment, please contact help@nrgr.on.spiceworks.com and reference your active access approval ID.
  • For more information, visit the CAPS homepage.

PGC

MULTIPLE

  • Full genome screen, 12,015 markers. 1,546 subjects. Data is provided by Anna Need from multiple studies: Study 0 (123 subjects), Study 12 (69 subjects), Study 15 (42 subjects), Study 22 (549 subjects), Study 23 (119 subjects), Study 29 (207 subjects), and Study 6 (398 subjects).  There are 39 subjects in Dr. Anna Need's genotype file but are not included in Schizophrenia Dist. 9.0.

MULTIPLE

  • 7,584 markers on chr 1-22. 639 subjects. Data is provided by Dr. Mark Brennan from multiple studies.  It includes 424 subjects from CATIE (study 17) and 215 subjects from GAIN.

Study 3

  • 375 Markers on Chromosome 1 to Chromosome 22, 15 Markers on Chromosome X. 2,405 subjects.

Study 6

  • 401 markers, STRP genotype data from Chromosome 1-23, for 1,422 African American and European American subjects

Study 9

  • Full Genome Screen of 1,323 subjects, Illumina 2.5M4; 2.5M8; 550k v1, v2; 610k; 660k

Study 13

  • Full Genome Screen - Escamilla 2003 Linkage Data. 434 subjects.
  • Full Genome Screen - Escamilla 2005 Linkage Data. 868 subjects.

Study 15

  • Chromosomes 1-22, 386 Microsatellite Markers and 93 SNP Markers. 616 subjects.

Study 17

  • CATIE Genome-Wide Association Data. Case-Control. PLINK files from Affymetrix 500k platform. 741 cases, 751 controls.
  • CATIE Genome-Wide Association Data, 291 cases. PLINK files from Affymetrix 6.0 platform. CEL files and CHP files are sent by request due to the large size of the files. To request shipment, please contact help@nrgr.on.spiceworks.com and reference your active access approval ID.

Study 22

  • Full Genome Screen - PAARTNERS. 5,756 markers. 787 subjects.

Study 90

  • GWAS from Ireland, 3,878 subjects. This dataset is available by request due to the large size of the files, including an archive of genotypes, .cel files, and diagnostic clinical information for the existing samples. Please contact help@nrgr.on.spiceworks.com and reference your active access approval ID.

SZ0

  • Full Genome Screen, Alternate version of SZ Dataset 8.01. 455 markers, 261 subjects.
  • Full Genome Screen. 624 markers, 109 subjects.
  • Full Genome Screen, alternate version of SZ Dataset 1.03. 455 markers, 261 subjects.

SWEDEN

  • No samples hosted at NIMH Repository and Genomics Resource. This dataset is hosted for public download by request of Pat Sullivan. Data from multi-stage genome-wide association study (GWAS) for schizophrenia beginning with a Swedish national sample (5,001 cases and 6,243 controls) followed by meta-analysis with previous schizophrenia GWAS (8,832 cases and 12,067 controls) and finally by replication of SNPs in 168 genomic regions in independent samples (7,413 cases, 19,762 controls and 581 parent-offspring trios).

MULTIPLE

  • 14 Genes, 648 SNPs Markers. 1870 cases, 2002 controls. Subjects from multiple studies (NIMH SZ study 0, study 6, study 29).

MULTIPLE

  • 240 SNPs, 42 genes, on Chromosomes 1-6, 8-13, 22, X, Y. 761 subjects from multiple studies (NIMH SZ study 0, study 6, study 12).

Study 3

  • PLXNA2 Gene, 3 Microsatellite Markers and 4 SNPs Markers on Chromosome 1. 1,143 subjects.

Study 76

SZ0

  • 13 markers on chromosome 4, 14 markers on chromosome 22, and 3 SNPs and 1 microsatellite marker in the Sult 4A region on chromosome 22. 169 subjects.
  • 5 BDNF Markers. 42 subjects.
  • 21 Markers on Chromosome 4 and 43 Markers on Chromosome 22. 225 subjects.
  • Syn2 Gene, 4 Microsatellite Markers and 11 SNPs Markers on Chromosome 3. 231 subjects.
  • Alpha2B Adrenoceptor for 26 Trios, 78 subjects.
  • 10 Markers for Chromosome 22, 429 subjects.
  • hKCa3 on Chromosome 1q21, 240 subjects.
  • 9 Markers on Chromosome 6, 371 subjects.
  • 3 Markers on Chromosome 15, 182 subjects.
  • K274E Mutation in PAH, 68 subjects.
  • Aromatic amino acid hydroxylase genes 8 markers for PAH, TPH, TH. 69 subjects.

Study 94

  • CIAC case-control data. This dataset is available by request due to the large size of the files, including Whole-Exome Sequencing (Illumina HiSeq2000 - 443 subjects, 67 cases), Illumina HumanExome BeadChip (Exome Chip - 319 subjects, 113 cases), Illumina OmniExpress BeadChip (GWAS Chip - 384 subjects, 135 cases) data. Please contact help@nrgr.on.spiceworks.com and reference your active access approval ID.

SZ0

  • Exome Sequence data (ABI SOLiDv4) on 12 family cases from sites 30 & 32, Dr. Debby Tsuang. BAM files are shipped upon request due to the large size of the files. To request shipment, please contact help@nrgr.on.spiceworks.com and reference your active access approval ID.

MULTIPLE

  • Next Generation Sequencing of Two Genes on chr 8 (EGR3 and ARC), 4,066 subjects. This data is available by request due to the large size of the files.  To request shipment, please contact help@nrgr.on.spiceworks.com and reference your active access approval ID.

Diagnostic Interview for Genetic Studies (DIGS) - The CSV-format DIGS interview files provided below are cleaned versions of those received from the original study investigators. While they retain the record layouts and variable naming of their respective DIGS versions, they have had invalid values corrected or removed, date fields converted to a standard format, and their various missing/ unknown values converted to standard textual metavalues in order to avoid misinterpretation. Further details on the cleaning that has been performed are included in the file "sz-digs-cleaning-readme.txt" included in the download. To download the original files as received from study investigators, use "original" links below.

Study 3

The DIGS data for Study 3a (Site 35) was collected by using DIGS Version 2.0.

Study 6

The DIGS data for Study 6 (Sites 41-49) was collected by using DIGS Version 2.1.

Study 12

The DIGS data for Study 12 (Site 33) was collected by using DIGS Version 2.0.

Study 13

The DIGS data for Study 13 (Sites 53, 54, 55, 56, 57, 58, 59) was collected by using DIGS Version 2.0 or 2.1.

Study 15

The DIGS data for Study 15 (Sites 70, 71) was collected by using DIGS Version 2.0.

Study 22

The DIGS data for Study 22 (Sites 101-108) was collected by using DIGS Version 3.0 and Version 4.0.

Study 23

The DIGS data for Study 23 (Site 73) was collected by using DIGS Version 2.0.

Study 29

The DIGS data for Study 29 (Sites 139-149) was collected by using DIGS Version 2.2.

Study 42

The DIGS data for Study 42 (Site 185) was collected by using DIGS Version 3.0 Revised 7.

Study 59

DIGS data for study 59 is in Comprehensive Assessment of Symptoms and History (CASH) format.

Study 92

DIGS data for Study 92 (Sites 320-321) were collected by using DIGS Version 2.0

SZ0

The DIGS data for Study 0 (Sites 30, 31, 32) was collected by using DIGS Version 1.0 or 2.0, both versions have a core of variables in common.

Study 9

Study 27

  • Includes anti-saccade performance data, demographics, GAF, WRAT, and CVLT summary scores, and a number of Cognitive accuracy & speed scores.
  • Includes anti-saccade performance data, demographics, GAF, WRAT, and CVLT summary scores, and a number of Cognitive accuracy & speed scores.

Study 42

Study 67

  • Extended diagnosis file (DSM4 codes) and Study-provided diagnosis definitions

Study 68

Study 76

  • Includes OPCRIT data, extended diagnosis file (DSM4), and study-defined diagnosis file.

Study 85

Study 94

  • Data on presence of absence of granulocytes during treatment with clozapine, for both cases and controls

Study 122

  • Study-specific diagnosis definitions and blank interview forms.

Study 17

  • Clinical Antipsychotic Trials of Intervention Effectiveness data, Including SCID, family interviews, laboratory results, adverse event reports, and more.

Study 22

Study 72

  • Including demographics, physical & medical exam, SCID, BPRS, CGI, medication logs, adverse event reports, and more.

Study 104