Miscellaneous

Dec
28
2009

SPOT link added

SNP Prioritization Online Tool link on Links page.

22q11.2 Deletion Syndrome

Feb
23
2017

22q11.2 Deletion Syndrome

22q11.2 Deletion Syndrome Dist. 1.0 includes data from NIMH Study 111 (PI: Kates). Included in this collection are a total of 64 individual cases; all 64 subjects with cell_line and 58 have plasma available.

Alzheimer's Disease

Mar
10
2016

Alzheimer's Disease Dist. 3.0

Alzheimer's Disease Dist. 3.0 added 185 subjects from Study 17/Site 75 (CATIE-AD).
Mar
30
2010

AD Dataset 20 Addition

Full Genome Screen / Total genotypes = 78,408

Attention-Deficit Hyperactivity Disorder (ADHD)

May
13
2010

ADHD Dist. 1.0

ADHD Dist. 1.0 contains 5,734 records in 1,331 families from Study 25.

Anorexia Nervosa

Feb
07
2012

Anorexia Nervosa Dist. 1.01

Anorexia Nervosa Dist. 1.01 contains 2,031 records in 412 families from Study 24, including dummypedigree connector records. N=1205 subjects have blood samples. Version 1.01 updates the Version 1.0 data by conforming the data to a standard format and correcting errors.
Feb
27
2009

Anorexia Nervosa Dist. 1.0

Anorexia Nervosa Dist. 1.0 contains 412 families from Study 24

Autism

Oct
12
2016

Autism Dist. 14.0

Autism Dist. 14.0 includes data from NRGR Study 56 (PI: Thurm), Study 60 (PI: Piven), Study 86 (PI: Haines), and Study 112 (PI: Devinsky). This collection contains 5,285 families and 21,466 individuals of which 18,822 have DNA cell lines. New in this collection are a total of 495 families (1,840 individuals, 1,646 with DNA). The Autism Dist. 14.0 Control dataset has the same format as the main distribution file and contains 254 families and 765 individuals of which 516 have DNA cell lines.
Sep
22
2015

Autism Dist. 13.0

Autism Dist. 13.0 includes new data from NIMH Study 39 (PI: Brzustowicz), Study 63 (PI: Cook), and Study 69 (PI: Minshew). This collection contains 4,793 families and 19,359 individuals of which 17,189 have DNA cell lines. New in this collection are a total of 360 families (1,303 individuals, 1,059 with DNA).
Apr
23
2015

Autism Dist. 12.01

Autism Dist. 12.01 added new psychiatric instrument data from NIMH Study 50 (PI: Coon) on the same set of subjects as Autism Dist. 12.0.
Jun
19
2014

Autism Dist. 12.0

Autism Dist. 12.0 includes new data from Study 44 (PI: Sutcliffe) and Study 50 (PI: Coon). This collection contains 4,434 families and 18,059 individuals of which 16,130 have DNA cell lines. New in this collection are a total of 182 families (564 individuals, 439 with DNA) from Study 44 (n=397 individuals) and Study 50 (n=167 individuals). The new data from Study 50 represents an update to the original deposit in Autism Dist. 9.0 (as Study 50) and in Autism Dist. 10.0 (as a component study of Study 65/TASC/AGP).
Mar
31
2014

Autism Dataset 4 Addition

Study 65 / TASC GWAS Data
Apr
23
2013

Autism Dist. 11.0

Autism Dist. 11.0 includes new data from Study 79 (aka Autism Consortium, Boston Autism Consortium, PIs: Kunkel, Walsh). This collection contains 4,278 families and 17,496 individuals of which 15,673 have blood samples. New in this collection are 316 families (1,169 individuals, 1,048 with blood) from Study 79.
Oct
25
2012

Autism Dist. 10.0

Autism Dist. 10.0 includes new data from Study 65 (aka TASC = The Autism Simplex Collection, PI: Gallagher). This new collection contains 3,962 families and 16,327 individuals of which 14,625 have blood samples. There are 1,339 families (4,298 individuals) from TASC, which represents approximately 80% of the total TASC data. The remaining 20% is undergoing preparation by the TASC DCC and will be available at a later date.
Apr
24
2012

Autism Dist. 9.0

Autism Dist. 9.0 includes new data from Study 50 (PI: Coon, Utah families). This study contains 2,930 families and 12,990 individuals of which 11,496 have blood samples.
Jun
09
2011

Autism Dist. 8.0

Autism Dist. 8.0 includes new data from Study 35 (Pericak-Vance, Molecular and Genetic Epidemiology of Autism). This study adds 409 affected subjects plus related family members for a total n=1337 of which n=1218 have blood samples.
Nov
15
2010

Autism Dist. 7.01

Autism Dist. 7.01 excludes one family (202-2922) with a subject who failed to meet Autism Spectrum Disorder criteria (per AGRE clinical staff).
Oct
28
2010

Autism Dist. 7.0

Autism Dist. 7.0 includes new data from AGRE. This study adds 724 affected subjects plus related family records (2069). It also includes updates to subjects in the Distribution 6.0 data.
Sep
01
2008

Autism Dist. 6.0

Autism Dist. 6.0 includes new data from Study 41. This study adds 169 affected subjects plus related family records (514 total). It also includes a few updates to Dist. 5.0 data.
Jun
01
2008

Autism Dist. 5.0

Autism Dist. 5.0 includes contributions from Version 4.1 sites, some of which has been updated, as well as data from seven new sites.
Feb
29
2008

Autism Dataset 3 Addition

GWAS data on 1,264 non-AGRE samples

Bipolar Disorder

Oct
13
2016

Bipolar Disorder Dist. 11.2

Bipolar Disorder Dist. 11.2 standardized variables in distribution file.
Nov
19
2015

Bipolar Disorder Dist. 11.1

Bipolar Disorder Dist. 11.1 made corrections for dx variable: 1351 subjects from Study 77 whose dx code should be SAB not SABP. Adjusted variables in standard and auxiliary files.
Nov
02
2015

Bipolar Disorder Dist. 11.0

Bipolar Disorder Dist. 11.0 includes new data from Study 75 (PIs: Nierenberg, Calabrese, Iosifescu, et al; R01HS01937101). Study 75 added new data for 193 subjects.
Oct
07
2015

Bipolar Disorder Dist. 10.4

Bipolar Disorder Dist. 10.4 fixed d4dx5 for subject 174-1251-001 from 303.90 to 301.9.
Jul
06
2015

Bipolar Disorder Dist. 10.3

Bipolar Disorder Dist. 10.3 fixed DSM-IV/DSM-III-R coding except for codes ending with x, added variables idc9 dx, icd9 dx age onset, and icd9 dx confidence.
Jun
28
2015

Bipolar Disorder Dist. 10.2

Bipolar Disorder Dist. 10.2 fixed none-standard DSM-IV coding plus posted standard and auxiliary files.
May
12
2015

Bipolar Disorder Dist. 10.1

Bipolar Disorder Dist. 10.1 fixed none-standard DSM-IV coding.
Mar
19
2015

Bipolar Disorder Dist. 10.0

Bipolar Disorder Dist. 10.0 includes new data from Study 77-Part 1 (PIs: Smoller, Skar, Pato, et al; R01MH085542) and Study 123 (PI: Swartz; R01MH084831). Study 77-Part 1 added 4,493 subjects and Study 123 added 38 subjects.
Jan
22
2015

Bipolar Disorder Dist. 9.1

Bipolar Disorder Dist. 9.1 updates the distribution files with the addition of plasma variable.
Sep
25
2014

Bipolar Disorder Dist. 9.0

Bipolar Disorder Dist. 9.0 includes data from Study 71 (PIs: Freimer, Macaya, el al; R01MH075007) and added 139 new subjects (143 subjects had a change to dx) from Study 1.
May
28
2014

Bipolar Disorder Dist. 8.0

Bipolar Disorder Dist. 8.0 includes new data from Study 55 (PIs: Nurnberger, Kastelic, McInnis, Reich, Glowinski; R01MH068009). There are 533 subjects from 210 families in Study 55 with 325 subjects with DNA available.
Aug
21
2013

Bipolar Disorder Dist. 7.01

Bipolar Disorder Dist. 7.01 includes updated data from Study 49 based on the data harvest revised as of Dec. 2012 and genotyped data received June 2013. 6329 subjects from 803 families were in Study 49. 2681 of 6329 subjects have DNA available.
Jul
30
2013

BP Dataset 29 Addition

BP Dataset 29 Addition (SNP Linkage Genotyping Data). Raw and partially cleaned data from Michael Escamilla for NIMH Study 49. Cleaned genotyping data was added on August 14, 2013.
Feb
07
2013

BP Dataset 28 Addition

BP Dataset 28 Addition (STEP-BD)
Oct
15
2012

Bipolar Disorder Dist. 7.0

Bipolar Disorder Dist. 7.0 includes new data from Study 49 based on the data harvest as of June 2012. 7730 subjects from 755 families were added, 2541 of 7730 subjects have DNA available.
Aug
06
2012

BP Dataset 27 Addition

Chromosomes 1-22 (SureGene - Custom Illumina iSelect chip containing 7,584 SNPs)
Oct
25
2011

Bipolar Disorder Dist. 6.02

Added auxiliary files for Bipolar Disorder Dist. 6.02 - list of subjects in GWAS (GAIN and non-GAIN).
Feb
18
2011

Bipolar Disorder Dist. 6.02

Dist. 6.02 includes updates to Study 40 subjects based on the final data harvest. An additional 210 subjects are included. Of the 240 subjects, 99 did not meet the diagnostic criteria for Bipolar Model I, II, or III categories, but were included for consistency with the GAIN analysis.
Jan
03
2011

Bipolar Disorder Dist. 6.01

a) Site 78 individual ids were revised for consistency with genotype files.
b) Variable length for dx variables d3rdx1-d3rdx8 were extended to correct truncating.
c) A flag was added for subjects with DIGS phenotype data.
d) Study number revised for sites 10-13 to Study=0.
e) Father_id 11-99002 was replaced as 11-10049.
f) Father_id 22-10159 dropped due to IRB issue. Re-assigned as 22-10199.
g) Cell_id for individual id 24-10222 corrected to 00C02884 per notification from Rutger's Cell and DNA Repository.
Nov
10
2010

BP Datasets 21-26 Added

BP Dataset 21 (G72Reseq), BP Dataset 22 (TRAR), BP Dataset 23 (Choline), BP Dataset 24 (Circadian 1 & 2), BP Dataset 25 (Neurotrans), BP Dataset 26 (Neurotrans)
Apr
05
2010

BP Dataset 17 Addition

STEP-BD Genotypic Data (STEP-BD / Chr6)
Apr
01
2010

BP Dataset 16 Addition

BP Dataset 16 Addition(STEP-BD)
Mar
31
2010

BP Dataset 16 Addition

STEP-BP Genotypic Data
Mar
10
2010

BP Dataset 20 Addition

Full Genome Screen / Total genotypes = 148,512
Mar
10
2010

BP Dataset 15 Addition

Ankyrin 3 (ANK3)
Sep
25
2009

Bipolar Disorder Dist. 6.0

Bipolar Disorder Dist. 6.0 includes 6,080 independent cases, including 1,829 new cases from the STEP-BD longitudinal study. It also includes 871 sib pairs with DNA from the previous distribution.
Jul
01
2009

BP Dataset 11 Phase 2 Addition

Pritzker 550K Illumina SNPs Phase 2
Jun
22
2009

Bipolar Disorder Dist. 5.0

Bipolar Disorder Dist. 5.0 adds over 3,700 cases for Study 40, most of which have no parents since it was a case-control study design (analysis compared affected to controls). There are 187 trios but pedigree drawings are not necessary for them. Study 40 used a new form of the DIGS, version 4.0, therefore, we had to add new separate DIGS files and documentations.
May
28
2009

BP Dataset 14 Addition

Chromosomes 1-6, 8-13, 22, X, Y
Mar
17
2009

NIMH_ID and GAIN_ID Cross-Reference

This file provides the NIMH_ID and GAIN_ID for subjects included in the GAIN (Genetic Association Information Network) bipolar disorder study.
Jul
17
2008

BP Dataset 13 Addition

Chromosomes 5q and 8p / bipolar disorder, GRIA1
May
06
2008

BP Dataset 12 Addition

P14K2b on Chromosome 4 / CERK, SULT4, BRD1, all genes on Chromosome 22
Apr
02
2008

BP Dataset 6-11 Additions

BP Dataset 6: 30 markers on 6 Chromosomes - trace amine receptors; BP Dataset 7: 62 SNPs on Chromosomes 3, 4, 11, 12, 18, 19, 22; BP Dataset 8: 19 SNPs on Chromosomes 1, 2, 11, 12, 17; BP Dataset 9: 93 SNPs on Chromosomes 1, 2, 4, 7, 8, 10, 11, 15, 17, 20; BP Dataset 10: 1004 SNPs on Chromosomes 1-13, 15-17, 19-23; BP Dataset 11: Pritzker 550K Illumina SNPs Phase 1
Feb
25
2008

Bipolar Disorder Dist. 4.02

Bipolar Disorder Dist. 4.02 includes one new artificial record added to make a family pedigree drawing possible.
Feb
13
2008

Bipolar Disorder Dist. 4.01

Bipolar Disorder Dist. 4.01 omits 8 records due to IRB issues.
Jul
31
2007

Bipolar Disorder Dist. 4.0

Bipolar Disorder Dist. 4.0 includes new data from an additional site that includes 281 records of newly identified independent cases and parent records from previous distribution versions 1.0 to 3.05.

Brain Function

Jul
05
2016

Brain Function Dist. 1.1

Brain Function Dist. 1.1 standardizes variables in Dist. 1.0.
Mar
17
2015

Brain Function Dist. 1.0

Brain Function Dist. 1.0 includes data from Study 109 (PI: Milham).

CommonMind Consortium

Oct
11
2016

CommonMind Consortium Dist. 1.2

CommonMind Consortium Knowledge Portal Release 1.2 data is now available.
Sep
16
2015

CommonMind Consortium Dist. 1.1

CommonMind Consortium Knowledge Portal Release 1.1 data is now available.
Mar
19
2015

CommonMind Consortium

CommonMind Consortium data access information was added.

Controls

May
07
2015

CN Dataset 3

SICCA NIMH only (Illumina 2.5M SNPs) added to Controls Dist. 8.0.
Mar
23
2015

Controls Dist. 8.0

Controls Dist. 8.0 includes new data for unaffected subjects from Study 76 and Study 77.
Jan
22
2015

Controls Dist. 7.05

Controls Dist. 7.05 updates the distribution files with the addition of plasma variable.
Sep
11
2012

Controls Dist. 7.04

Controls Dist. 7.04 adds gender of Study 19/Site 88 subjects.
Aug
25
2011

Controls Dist. 7.03

Controls Dist. 7.03 restores 3 records that were in Dist. 5.0 and were removed from Dist. 6.01-7.02 because of known race or sex discrepancy.
Jul
07
2011

Controls Dist. 7.02

Controls Dist. 7.02 added diagnostic algorithms and updated phenotypic data.
Dec
28
2010

Controls Dist. 7.01

Controls Dist. 7.01 restores 49 records that were on Dist. 5.0 and inadvertently omitted from Dist. 6.0 and 7.0.
Nov
01
2009

Controls Dist. 7.0

Controls Dist. 7.0 includes new data for 105 unaffected adults from Study 23.
Oct
24
2008

NIMH_ID and GAIN_ID Link

Addition of link between NIMH_ID and GAIN_ID in Controls Dist. 6.12.
Aug
08
2008

Controls Dist. 6.12

Controls Dist. 6.12 omits 24 records where genotyped race values were inconsistent with reported phenotypic values, and includes one new record with phenotypic information.
Mar
20
2008

CN Dataset 1

Raw .CEL files available for all samples genotyped using the Affymetrix GeneChip Human 500K Mapping Array Set
Feb
13
2008

Controls Dist. 6.11

Controls Dist. 6.11 includes corrections to sex for 4 subjects, omits 7 subjects due to unresolved discrepancies in reported sex vs. genotyped sex, omits 2 records for which DNA was unavailable, and omits 47 duplicate records.
Feb
01
2008

Controls Dist. 6.1

Controls Dist. 6.1 omits 22 records that were included in Dist. 6.0, but had a Did Not Grow status from blood records.
Nov
13
2007

CN Dataset 2 (Illumina SNPs)

Controls Dataset 2 updated with new file from Illumina
Oct
30
2007

CN Dataset 2 (Illumina SNPs)

Data file for Controls Dataset 2 reissued
Oct
01
2007

Controls Dist. 6.0

Controls Dist. 6.0 includes a total of 5212 cases. Phenotyping screening data is available for 4664 of these records.
Aug
21
2007

Control Questionnaire access

Control Questionnaire no longer password protected

Depression

Oct
17
2014

Depression Dist. 5.0

Depression Dist. 5.0 adds new data from Study 20 (TADS [PI: March] and SOFTAD [Curry]) and Study 73 (CO-MED [PI: Trivedi]). This collection contains 11,217 individuals in 5,253 families. 7,194 individuals have DNA cell lines and 175 individuals have plasma available. 171 individuals from Study 20 and 478 individuals from Study 73 were added to this distribution.
May
20
2014

Depression Dist. 4.0

Depression Dist. 4.0 contains 10,568 individuals in 4,606 families from Studies 7 (GenRED I), 52 (GenRED II), 18 (STAR*D), and 88 (Depression Genes Network [DGN]). 6,545 individuals have DNA cell lines. 463 cases from Study 88 were added and 459 controls were collected for this study.
Apr
21
2014

DP Dataset 7 Addition

Levinson RNA Sequencing data from Study 88/Site 621
Mar
14
2012

DP Dataset 6 Addition

STAR*D/Study 18
Feb
07
2012

Depression Dist. 3.02

Depression Dist. 3.02 contains 10,105 records in 4,141 families from Studies 7, 52, and 18 (STAR*D). 8,163 records in 2,199 families were in the previous distribution (version 3.01), 1,942 records in 1,942 families from Study 18 (STAR*D/Site 77).
Oct
07
2011

Depression Dist. 3.01

Depression Dist. 3.01 corrects errors in the Study 52 DIGS and auxiliary files; otherwise, it is identical to Dist. 3.0.
Jan
24
2011

Depression Dist. 3.0

Depression Dist. 3.0 contains 8,163 records in 2,199 families from Study 7 (GenRED I) and Study 52 (GenRED II), including dummy pedigree connector records and counting singletons as a family. Dist 3.0 adds Study 52 subjects to the Study 7 data.
Nov
02
2010

DP Dataset 4.01

Added information for controls
Aug
24
2010

DP Dataset 5 Addition

88 GenRED Markers
Jun
11
2010

DP Dataset 4 Addition

GenRED
Jan
24
2009

STAR*D Mapping

Addition of STAR*D IDs mapping text file
Nov
05
2008

Depression Dist. 2.0

Depression Dist. 2.0 includes the addition of the STAR*D clinical data and genotypes.
Sep
04
2008

DP Dataset 1 Addition

GenRED 92 SNPs markers

Fear & Anxiety

Dec
10
2015

Fear & Anxiety Dist. 1.0

Fear and Anxiety Dist. 1.0 includes data from Study 61/Site 137 (PIs: Weissman, et al.) and Study 62/Site 138 (PIs: Fyer, et al.). This new collection contains 320 cases from Study 61 (no plasma) and 60 controls from Study 61 plus 197 subjects (no dx) from Study 62 (no plasma).

Induced Pluripotent Stem Cells (iPSC)

Jan
25
2017

iPSC Dist. 6.0

iPSC Dist. 6.0 includes data from Study 92/Sites 322-323 (PIs: Gur, Nimgaonkar) and Study 160/Site 504 (PI: Brennand). In Study 92, there are 130 individuals from 130 families, 0 iPSCs, and 174 fibroblasts. In Study 160, there are a total of 41 iPSCs, 0 fibroblasts. Also, 11 cases from Study 132/Site 499 (PI: Rapoport) were updated with iPSCs; 11 controls.
Jul
11
2016

iPSC Dist. 5.0

iPSC Dist. 5.0 includes data from Study 158/Site 361 (PIs: Brennand, Gage). There are 11 individuals from 10 families, 13 iPSCs, and 0 fibroblasts for a total of 280 subjects.
Apr
23
2015

iPSC Dist. 4.0

iPSC Dist. 4.0 includes data from Study 143/Site 408 (PI: Muotri) and Study 144/Site 738 (PIs: Muotri, Duvvuri). In Study 143, there are 8 individuals from 8 families, 21 iPSCs, and 13 fibroblasts, and in Study 144, there are 17 individuals from 17 families, 43 iPSCs, and 23 fibroblasts for a total of 269 individuals. Also, updated data from Study 116 and Study 125.
Jul
17
2014

iPSC Dist. 3.0

iPSC Dist. 3.0 includes data from Study 132/Site 499 (PI: Rapoport). There are 184 individuals from 59 families, 0 iPSCs, and 184 fibroblasts for a total of 242 individuals.
Mar
20
2014

iPSC Dist. 2.0

iPSC Dist. 2.0 includes data from Study 116/Site 727 (PI: Vaccarino). There are 19 individuals from 6 families, 25 iPSCs, and 19 fibroblasts for a total of 58 individuals.
Feb
20
2014

iPSC Dist. 1.0

iPSC Dist. 1.0 includes data from Study 115/Sites 726 and 734 (PIs: Hallmayer, Dolmetsch; Phelan McDermid Foundation), Study 117/Site 728 (PI: Loring; Fragile X-Autism), and Study 125/Sites 392-393 (PIs: Lachman, Rapoport; 22q11 Deletion Syndrome). There are 20 individuals from 17 families, 4 iPSCs, and 20 fibroblasts in Study 115. There are 4 individuals from 4 families, 8 iPSCs, and 0 fibroblasts in Study 117. There are 15 individuals from 15 families, 16 iPSCs, 0 fibroblasts in Study 125 for a total of 39 individuals.

Netherlands Twin Register (NTR)

Mar
22
2012

NTR Dist. 2.0

NTR Dist. 2.0 includes 9,123 subjects with Rutgers IDs and their families from Study 78 (number of families=3,655; total=11,900 subjects).

Obsessive-Compulsive Disorder (OCD)

Oct
25
2016

Trichotillomania Dist. 1.1

Trichotillomania Dist. 1.1 standardizes variables.
Sep
12
2016

OCD Dist. 2.4

OCD Dist. 2.4 standardizes distribution file.
Jul
15
2015

Trichotillomania Dist. 1.0

Trichotillomania Dist. 1.0 adds new data from Study 134/Site 508 (PI: Keuthen) and includes 513 individuals from 295 families and 419 individuals have cell lines.
Jun
09
2015

Compulsive Hoarding Dist. 1.0

Compulsive Hoarding Dist. 1.0 adds new data from Study 93/Site 245 (PI: Mathews) and includes 102 individuals from 60 case families and 41 individual controls.
Jan
22
2015

OCD Dist. 2.3

OCD Dist. 2.3 updates the distribution files with the addition of plasma variable.
Sep
26
2014

OCD Dist. 2.2

OCD Dist. 2.2 updates Study 66 with the latest blood file. Added 8 pedigrees and removed one. Total 5,656 individuals in 1,490 families.
Aug
28
2014

OCD Dist. 2.1

OCD Dist. 2.1 fixes 2 subject's cell_ids and ind_ids (in blood file).
May
08
2013

OCD Dist. 2.0

OCD Dist. 2.0 includes data from Study 66 (sites 240-244). There are 1,156 new families and 3,921 new individuals for a total of 1,483 families and 5,634 individuals.
Mar
16
2009

OCD Dist. 1.0

OCD Dist. 1.0 includes data from Study 16 (sites 64-69). There are 327 families and 1,713 individuals.

Phelan-McDermid Syndrome (PMS)

Jun
02
2016

PMS Dist. 1.1

PMS Dist. 1.1 standardizes variables in Dist. 1.0 and adds auxiliary files.
Apr
15
2014

PMS Dist. 1.0

PMS Dist. 1.0 includes data from Study 115/Sites 726 and 734 (PIs: Hallmayer, Dolmetsch; Phelan McDermid Foundation). There are 165 individuals from 55 families. There are 55 probands.

PsychENCODE Consortium

Aug
31
2016

PsychENCODE Consortium Dist. 2.0

PsychENCODE Consortium data release for August 2016.
Feb
02
2016

PsychENCODE Consortium Dist. 1.0

PsychENCODE Consortium data access information was added.

Schizophrenia

Dec
22
2016

SZ Dist. 17.0

Schizophrenia Dist. 17.0 includes new data from Study 94 (CIAC: PIs: Sullivan, et al.) and released genotype data for Study 94 in SZ Dataset 31.
New in this collection are a total of 482 individuals in 482 families from Study 94 (270 individuals have DNA cell lines available; 251 individuals have plasma available). Also released was the genotype data for Study 94 in SZ Dataset 31.
Apr
27
2016

SZ Dist. 16.0

Schizophrenia Dist. 16.0 includes new data from Study 72 (PROACTIVE: PIs: Miller, et al.) and Study 104 (ACLAIMS; PIs: Stroup, et al.). New in this collection are a total of 363 individuals in 363 families from Study 72 and Study 104 (360 individuals have DNA cell lines available; 176 individuals have plasma available).
Feb
03
2016

SZ Dist. 15.0

Schizophrenia Dist. 15.0 includes new data from Study 82 (PIs: Ming T. Tsuang, Stephen J. Glatt, et al.). New in this collection are a total of 9,097 individuals in 3,003 families.
Oct
01
2015

SZ Dist. 14.0

Schizophrenia Dist. 14.0 includes new data from Study 27 (PI: David Braff), Study 68 (PI: Lynn DeLisi), and Study 85 (PI: Lynn DeLisi).
Jul
15
2015

SZ Dataset 30 Addition

Results of Next Generation Sequencing of Two Genes (EGR3 and ARC) in Schizophrenia from Dr. Amelia Gallitano, multiple studies and controls.
Mar
23
2015

SZ Dist. 13.0

Schizophrenia Dist. 13.0 includes new data for 9,276 individuals in 8,295 families from Study 76 (PI: Carlos Pato).
Feb
19
2013

SZ Dataset 29 Addition

Sweden Schizophrenia Study
Jan
26
2015

SZ Dist. 12.01

SZ Dist. 12.01 updates the auxiliary files within the addition of plasma variable.
Dec
17
2014

SZ Dist. 12.0

SZ Dist. 12.0 includes new data for 830 case individuals and 1,478 controls from Study 9 (PIs: Weinberger, Straub). Diagnoses were obtained from medical records and clinical charts, no DIGS or SCID were performed for Study 9.
Feb
11
2014

SZ Dist. 11.01

The NPI algorithm was updated, variables NPI and NPISO were removed, and a variable DX (phenotype status) was added in the auxiliary file.
Dec
05
2013

SZ Dataset 28 Addition

Dr. Debby Tsuang Exome data from Sites 30 and 32 (Study 0)
Sep
30
2013

SZ Dataset 27 Addition

CATIE Genome-Wide Association Data
Sep
09
2013

SZ Dist. 11.0

SZ Dist. 11.0 includes new data for 99 families from Study 91 (PIs: Goldstein, McEvoy, Need). Diagnoses were obtained from clinical charts, no DIGS or SCID were performed for Study 91.
Jan
15
2013

SZ Dist. 10.0

SZ Dist. 10.0 includes new data for 260 families from Study 59 (PI: Ophoff). Also, 262 controls were collected for this study.
Aug
06
2012

SZ Dataset 26 Addition

Chromosomes 1-22 from multiple studies (SureGene)
Jun
25
2012

SZ Dataset 25 Addition

Full Genome Screen from multiple studies (PI: Anna Need)
May
16
2012

SZ Dist. 9.0

SZ Dist. 9.0 includes new data for 193 families from Study 42 (Pulver).
Oct
12
2010

SZ Dataset 24 Addition

Full Genome Screen from NIMH Study 22 - PAARTNERS
Oct
01
2010

SZ Dataset 23 Addition

Full Genome Screen from NIMH Study 13 - 2005 Linkage Data
Sep
30
2010

SZ Dataset 22 Addition

Full Genome Screen from NIMH Study 13 - 2003 Linkage Data
Sep
13
2010

SZ Dataset 21 Addition

Full Genome Screen from NIMH Study 15, 386 Microsatellite Markers and 93 SNP Markers
Apr
09
2010

SZ Dataset 11.01

Updated files
Mar
30
2010

SZ Dataset 1.02

Documentation changed substantially in that the missing markers on the maps for Chr 9 and 15 are documented and a proposed new marker order is included. The original map was not modified.
Mar
17
2010

SZ Dataset 1.01

Added Chr 22 map file
Mar
09
2010

SZ Dataset 20 Addition

Full Genome Screen / Total genotypes = 68,016
Dec
30
2009

Schizophrenia Dist. 8.0

Schizophrenia Dist. 8.0 includes new data for 138 families from Study 23.
Sep
30
2009

Schizophrenia Dist. 7.0

Schizophrenia Dist. 7.0 includes new data for 573 families from Study 22.
Jun
05
2009

SZ Dataset 19 Addition

240 Markers on Chromosomes 1-6, 8-13, 22, X and Y, 42 genes were included
Jul
31
2008

SZ Dataset 18 Addition

Total of 648 SNPs Markers, 14 genes (RGS4, DISC1, DTNBP1, STX7, TAAR6, PPP3CC, NRG1, DRD2, HTR2A, DAOA, AKT1, CHRNA7, COMT, ARVCF) were included for April 08 AJP paper from MGS project (Study 29)
Jul
21
2008

SZ Dataset 13

Addition of text version of data files
Jul
09
2008

Schizophrenia Dist. 6.0

Schizophrenia Dist. 6.0 includes new data for 3,848 families from Study 29. Families from Site 17 of Study 13 were excluded from Dist. 6.0.
May
06
2008

SZ Dataset 17 Addition

PLXNA2 Gene, 3 Microsatellite Markers and 4 SNPs Markers on Chromosome 1
Apr
11
2008

CATIE Clinical Data

CATIE clinical data posted on Schizophrenia Dist. 5.0
Mar
21
2008

SZ Dataset 16 Addition

Syn2 Gene, 4 Microsatellite Markers and 11 SNPs Markers on Chromosome 3
Mar
18
2008

Schizophrenia Dist. 5.0

Schizophrenia Dist. 5.0 includes new data from Study 13 and Study 15
Dec
03
2007

SZ Dataset 15 Addition

21 Markers on Chromosome 4 and 43 Markers on Chromosome 22
Sep
14
2007

SZ Dataset 14 Addition

5 BDNF SNPs Markers
Sep
14
2007

SZ Dataset 12 Addition

Addition of 15 Markers on Chromosome X
Sep
01
2007

Schizophrenia Dist. 4.0

Schizophrenia Dist. 4.0 includes new data from CATIE and Genome-Wide Association
Aug
03
2007

Schizophrenia Dist. 3.0

Genome linkage screen now available for Taiwan data

Suicide

Dec
08
2015

Suicide Dist. 1.1

Suicide Dist. 1.1 reorders and renames variables in the distribution file.
Nov
19
2015

Suicide Dist. 1.0

Suicide Dist. 1.0 includes data from Study 80/Sites 288-290 (PIs: Mann, Turecki, Rujesca). There are 181 subjects including 159 controls and 22 probands, 3 have plasma.

Tourette Syndrome

Nov
16
2016

Tourette Syndrome Dist. 1.2

Tourette Syndrome Dist. 1.2 corrected several genders.
Oct
26
2016

Tourette Syndrome Dist. 1.1

Tourette Syndrome Dist. 1.1 corrected dx from ChronicTic to TDChronicTic.
Oct
13
2016

Tourette Syndrome Dist. 1.0

Tourette Syndrome Dist. 1.0 includes data from Study 106/Sites 600-609 (PIs: Tischfield, Heiman, State, et al.). There are 2,981 subjects from 780 families; 2,647 subjects with cell lines and 2,152 subjects have plasma.