Neurodevelopmental disorders

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Unknown (7738)
Genomics (967)
Transcriptomics (590)
Proteomics (134)
Methylation profiling (36)
Other (33)
Metabolomics (14)
Genomic (13)

Organisms

Homo sapiens (434)
Mus musculus (363)
Schizosaccharomyces pombe (96)
Sinorhizobium meliloti BL225C (96)
Sus scrofa domesticus (96)
Saccharomyces cerevisiae (96)
Staphylococcus aureus (96)
Rattus norvegicus (96)
Escherichia coli (96)
Methylohalobius crimeensis 10Ki (96)
Homo sapiens (96)
Shigella flexneri (96)
Allexis (96)
Rattus norvegicus (32)
Drosophila melanogaster (14)
Danio rerio (8)
Macaca mulatta (4)
Caenorhabditis elegans (4)
Callithrix jacchus (2)
Saccharomyces cerevisiae (2)
Sus scrofa (2)
Mytilus galloprovincialis (1)
Pan troglodytes (1)
Oryctolagus cuniculus (1)
Human betaherpesvirus 5 (1)
Xenopus laevis (1)
Xenopus tropicalis (1)
Macaca fascicularis (1)
Mus (1)
Rattus rattus (1)

Organisms

Homo sapiens (311)
Mus musculus (285)
Rattus norvegicus (19)
Drosophila melanogaster (12)
Danio rerio (6)
Caenorhabditis elegans (4)
unidentified (3)
Callithrix jacchus (2)
Macaca fascicularis (2)
Sus scrofa (2)
Macaca mulatta (2)
Saccharomyces cerevisiae (2)
mouse gut metagenome (2)
Xenopus tropicalis (1)
Xenopus laevis (1)
Mus (1)
Mus musculus musculus (1)
gut metagenome (1)

Repository

ENA (799)
geo (610)
biostudies-arrayexpress (154)
pride (96)
EGA (62)
MassIVE (25)
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dbGaP (13)
iProX (9)
jPOST (4)
EVA (1)

Tissue

Brain (35)
Cell culture (25)
Embryonic stem cell (5)
Whole body (4)
Blood (4)
Neuronal stem cell (2)
Monocyte (2)
Neuron of the forebrain (1)
Neuron differentiation (1)
Neuron cellular homeostasis (1)
Capillary endothelial cell (1)
Neuronal cell line (1)
Generation of neurons (1)
Neuroblastoma cell (1)
Astrocyte of the cerebral cortex (1)
Gastrocnemius (1)
Neuron of cerebral cortex (1)
Pluripotent stem cell (1)
HEK-293T cell (1)
Kidney cell (1)
Muscle (1)
Early embryonic cell (1)
Neuron (1)
Blood plasma (1)
Stem cell (1)
Fibroblast (1)
Hippocampal neuron (1)
Permanent cell line cell (1)
Kidney (1)
T cell (1)

Disease

Autism spectrum disorder (3)
Rett syndrome (2)
Disease free (2)
Colon cancer (2)
Cockayne syndrome (1)
Spinal muscular atrophy (1)
Parkinson's disease (1)
Fetal alcohol syndrome (1)
Neurodevelopmental delay (1)
Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction (1)
Kabuki syndrome (1)
Neurodevelopmental disorder with or without autism or seizures (1)
Neurological dysfunction (1)
Fragile X syndrome (1)
Epilepsy (1)
Leigh disease (1)

Technology Type

Mass Spectrometry (96)
Shotgun proteomics (32)
Bottom-up proteomics (29)
Data-dependent acquisition (23)
Illumina HiSeq 2000 (18)
Affinity purification coupled with mass spectrometry proteomics (18)
Data-independent acquisition (11)
Mass spectrometry (9)
Illumina Genome Analyzer II, Illumina HiSeq 2000 (6)
Mass spectrometry assay (5)
Top-down proteomics (5)
SWATH MS (4)
Affinity proteomics (3)
HDMSE (3)
Gel-based experiment (3)
Illumina HiSeq 2000, Illumina Genome Analyzer II (2)
SRM/MRM (2)
Illumina HiSeq 2000, Illumina HiSeq 2000 (ILLUMINA) (1)
Illumina HiSeq 2000, ILLUMINA (1)
NMR spectroscopy (1)
SomaScan affinity proteomics (1)
Proteogenomics (1)
DiaPASEF (1)

Instrument Platform

Illumina NovaSeq 6000 (15)
Orbitrap Fusion Lumos (7)
Orbitrap Fusion (5)
Liquid Chromatography MS - positive - reverse phase (5)
Orbitrap Exploris 480 (4)
NextSeq 500 (3)
Illumina HiSeq 2000 (3)
Liquid Chromatography MS - negative - reverse phase (3)
NextSeq 2000 (2)
TimsTOF fleX (2)
LTQ Orbitrap Elite (2)
Orbitrap Eclipse (2)
Q Exactive HF (2)
Liquid Chromatography MS - (2)
Liquid Chromatography MS - positive - reverse-phase (2)
Liquid Chromatography MS - negative - reverse-phase (2)
Illumina NOVAseq 6000 (1)
Illumina NovaSeq X (1)
R (1)
Illumina MiSeq (1)
NextSeq 550 (1)
Illumina HiSeq 2500 (1)
Illumina HiSeq 4000 (1)
Q-Exactive( Thermo fisher) (1)
Fusion Lumos Tribrid (1)
Q-Exactive Plus (1)
LTQ Orbitrap Velos Pro (1)
TripleTOF 5600 (1)
Liquid Chromatography MS - Negative (LC-MS (Negative)) (1)
Liquid Chromatography MS - Positive (LC-MS (Positive)) (1)

Publication Date

2026 (165)
2025 (148)
2024 (123)
2023 (76)
2022 (61)
2021 (48)
2020 (46)
2011 (34)
2016 (27)
2015 (27)
2018 (27)
2014 (26)
2019 (23)
2013 (20)
2010 (19)
2017 (14)
2012 (13)
2008 (5)
2007 (5)
2009 (4)
2004 (1)

CHEBI ID

CHEBI:36005 (3)
CHEBI:28842 (3)
CHEBI:16196 (3)
CHEBI:15843 (3)
CHEBI:16811 (3)
CHEBI:18139 (2)
CHEBI:30768 (2)
CHEBI:28941 (2)
CHEBI:28822 (2)
CHEBI:30745 (2)
CHEBI:1427 (2)
CHEBI:28790 (2)
CHEBI:28875 (2)
CHEBI:16857 (2)
CHEBI:17895 (2)
CHEBI:16828 (2)
CHEBI:17115 (2)
CHEBI:28716 (2)
CHEBI:17295 (2)
CHEBI:17351 (2)
CHEBI:16414 (2)
CHEBI:30772 (2)
CHEBI:18101 (2)
CHEBI:28631 (2)
CHEBI:17203 (2)
CHEBI:18019 (2)
CHEBI:16934 (2)
CHEBI:15891 (2)
CHEBI:16865 (2)
CHEBI:15354 (2)

Metabolite Name

FA 10:0 (2)
PE 36:4|PE 16:0_20:4 (2)
PE 38:6|PE 16:0_22:6 (2)
PC 44:6 (2)
PC 38:4|PC 18:0_20:4 (2)
PC 30:3 (2)
PC 42:5 (2)
PC 40:6|PC 18:0_22:6 (2)
PC 38:6|PC 16:0_22:6 (2)
PC 36:2|PC 18:0_18:2 (2)
PC 36:4|PC 16:0_20:4 (2)
PC 34:2|PC 16:0_18:2 (2)
PE 40:6|PE 18:0_22:6 (2)
PE 38:4|PE 18:0_20:4 (2)
PG 34:1|PG 16:0_18:1 (2)
PE 36:3|PE 18:1_18:2 (2)
PE 34:2|PE 16:0_18:2 (2)
FA 22:0 (2)
FA 22:3 (2)
FA 22:4 (2)
FA 22:5 (2)
FA 22:6 (2)
FA 20:0 (2)
FA 20:1 (2)
FA 20:2 (2)
FA 20:3 (2)
FA 20:4 (2)
FA 20:5 (2)
FA 18:0 (2)
FA 18:1 (2)

First Public Date

2025 (161)
2026 (139)
2024 (120)
2023 (78)
2022 (59)
2021 (46)
2020 (46)
2014 (34)
2017 (30)
2019 (28)
2018 (19)
2016 (17)
2013 (12)
2015 (10)

Modification

N6 (1)
Not available (1)

Study type

Transcription profiling by array (67)
RNA-seq of coding RNA (32)
Methylation profiling by array (14)
Comparative genomic hybridization by array (10)
ChIP-seq (8)
RNA-seq of coding RNA from single cells (4)
Cell line - High-throughput sequencing (2)
DNA-seq (2)
Methylation profiling by high throughput sequencing (2)
RNA-seq of non coding RNA (2)
Human - High-throughput sequencing (1)
Human - One-color microarray (1)
Animal - High-throughput sequencing (1)
Transcription profiling by tiling array (1)
Genotyping by array (1)
Capture-C (1)
Transcription profiling by RT-PCR (1)
MicroRNA profiling by high throughput sequencing (1)
ATAC-seq (1)
Exome sequencing (1)
RIP-seq (1)

Release Date

2025 (1045)
2022 (974)
2023 (934)
2021 (862)
2024 (858)
2020 (657)
2019 (495)
2018 (418)
2017 (360)
2016 (279)
2015 (245)
2014 (196)
2026 (146)
2013 (108)
2011 (84)
2012 (82)
2010 (59)
2009 (33)
2007 (19)
2008 (14)
2006 (7)
2005 (6)
2004 (6)
2003 (3)
2001 (1)
2000 (1)

Lab affiliation

Department of Chemistry, Imperial College London, Molecular Sciences Research Hub, London, W12 0BZ, UK The Francis Crick Institute, London, NW1 1AT, UK (4)
Department of Genetic Medicine and Development, Faculty of Medicine, University of Geneva, Switzerland (2)
IRCCS Istituto G Gaslini (2)
University of Edinburgh (2)
Department of Pediatrics University of Maryland, School of Medicine (1)
Harvard Medical School Department of Neurobiology (1)
Keck MS & Proteomics Resource at Yale University Dept. MBB, Yale University (1)
Department of Physiological Sciences, University of Barcelona, IDIBELL, Spain (1)
The University of South Florida (1)
95 Institut de Pharmacologie et de Biologie Structurale (IPBS), Université de Toulouse, CNRS, Université Toulouse III - Paul Sabatier (UT3), Toulouse, 31077, France (1)
Inserm UMRS 1256 N-GERE (Nutrition-Genetics-Environmental Risks) (1)
Institute of Cellular Neurosciences II University of Bonn, Germany (1)
Center of Neurodevelopmental Disorders (KIND), Centre for Psychiatry Research, Department of Women’s and Children’s Health, Karolinska Institute, Region Stockholm, Stockholm, Sweden Astrid Lindgren Children’s Hospital, Karolinska University Hospital, Region Stockholm, Stockholm, Sweden (1)
Department of Chemistry, Imperial College London, Molecular Research Science Hub, 80 Wood Lane, London W12 0BZ, United Kingdom. The Francis Crick Institute, 1 Midland Road, London NW1 1AT, United Kingdom. (1)
Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China. Liangzhu Laboratory, MOE Frontier Science Center for Brain Science and Brain-Machine Integration, State Key Laboratory of Brain-Machine Intelligence, Zhejiang University, Hangzhou,China. (1)
Department of Anatomy and Neurobiology, School of Medicine, Virginia Commonwealth University, Richmond, VA USA (1)
Department of Neuroscience, Tufts University School of Medicine (1)
Genetic and Molecular Basis of Neurodevelopmental Disorders, IST Austria, Klosterneuburg, Lower Austria, Austria (1)
Institute of Structural Biology, Helmholtz Zentrum München - German Research Center for Environmental Health, 85764, Neuherberg, Germany; Institute of Pharmaceutical Biotechnology, 89081, Ulm University, Ulm, Germany. (1)
School of Pharmacy, University of Wisconsin-Madison, Madison, WI, 53705, USA (1)
Zilkha Neurogenetic Institute, University of Southern California, Los Angeles, CA, USA (1)
NeuroEpigenetics laboratory, Department of Cellular, Computational and Integrative Biology, University of Trento, Trento, Italy (1)
Institute for Research in Biomedicine (IRB Barcelona), The Barcelona Institute of Science and Technology, 08028 Barcelona, Spain (1)
Department of Biology, University of Ottawa, Ottawa, Canada, K1N 6N5 (1)
IGBMC, Institut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch, France, UMR7104, UMR-S 1258. (1)
Cologne Center for Genomics (CCG), University of Cologne, Faculty of Medicine and University Hospital Cologne (1)
Department of Fundamental Neurosciences, Université de Lausanne, 1005 Lausanne, Switzerland & Department of Biomedicine and Prevention, Università degli studi di Roma "Tor Vergata", 00133 Rome, Italy (1)
Philipps-University Marburg Department of Chemistry & Center for Synthetic Microbiology (SYNMIKRO) Karl-von-Frisch-Straße 14 35043 Marburg GERMANY (1)
LSMBO IPHC UMR7178 CNRS Université de Strasbourg (1)
LSMBO-IPHC UMR7178 CNRS University of Strasbourg (1)

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Elevated lysophosphatidylcholines during SSRI-induced neural differentiation correlate with early neurodevelopmental symptoms

Background: Selective serotonin reuptake inhibitors (SSRIs) are often prescribed during pregnancy. Yet, epidemiological studies link in-utero SSRI exposure with neurodevelopmental disorders, such as autism and ADHD. The potential molecular mechanisms by which SSRIs impact early n...

2026-04-02 | MTBLS12645 | MetaboLights

Array-CGH in a boy with an occurrence of neurodevelopmental disorders and epilepsy

This analysis includes the whole-genome screening of unbalanced chromosomal rearrangements (copy-number variants; CNV) in a boy with neurodevelopmental disorders and epilepsy.

ORGANISM(S): Homo sapiens

2020-01-31 | E-MTAB-8147 | biostudies-arrayexpress

Autoinhibition of Trio guanine nucleotide exchange factor activity for Rac1 by its spectrin repeats is disrupted by neurodevelopmental disorder-related genetic variants

Crosslinking MS of SR6-GEF1 construct of Human Trio. BS3 crosslinking of wild-type and three point mutants implicated in neurodevelopmental disorders (E883D, R1078Q, D1368V). Data acquired using FAIMS ion mobility source with each sample acquired at 4 different CVs (-40, -50, -60, -70V).

ORGANISM(S): Homo Sapiens (ncbitaxon:9606)

2022-06-08 | MSV000089621 | MassIVE

Gut Microbiota Mediates Maternal PM2.5 Exposure-induced Neurodevelopmental Disorder in offspring via Disturbing the Glutamate Metabolism: Evidence from Multiomics Analysis

While accumulating evidence links maternal PM2.5 exposure to offspring neurodevelopmental impairments, yet the underlying biological pathways require further elucidation. To address this, female ICR mice are exposed to filtered air (FA) or concentrated ambient particulate matter (CAP) for three ...

2026-01-05 | MTBLS13599 | MetaboLights

Alterations in gut microbiota composition, plasma lipids, and brain activity, suggest inter-connected pathways influencing malnutrition-associated cognitive and neurodevelopmental changes.

Malnutrition affects over 30 million children annually and has profound immediate and enduring repercussions, with nearly half of child deaths under five linked to malnutrition. Survivors face lasting consequences, including impaired neurocognitive development, leading to cognitive and behavioura...

2024-11-27 | MTBLS10066 | MetaboLights

Genome sequencing coupled with iPSC technology identifies GTDC1 as a novel candidate gene involved in Neurodevelopmental Disorders

We identified genomic structural alterations of six patients with signs of neurodevelopmental disorder (NDDs) that harbour chromosomal rearrangements using large-insert paired-end tag sequencing (DNA-PET). This technique allowed the refinement of chromosomal breakpoints and lead to the identificatio...

ORGANISM(S): Homo sapiens

2014-09-03 | E-GEOD-51430 | biostudies-arrayexpress

Targeted next-generation sequencing in family with an occurrence of neurodevelopmental disorders and epilepsy

We performed a targeted NGS using the commercial gene panel design ClearSeq Inherited Disease (Agilent Technologies) to identify the pathogenic sequence variants in two boys with neurodevelopmental disorders and epilepsy and their unaffected parents

ORGANISM(S): Homo sapiens

2019-12-31 | E-MTAB-8131 | biostudies-arrayexpress

GTF2I dosage regulates neuronal differentiation and social behavior in 7q11.23 neurodevelopmental disorders Organoid

Mice experiment for GTF2I dosage regulates neuronal differentiation and social behavior in 7q11.23 neurodevelopmental disorders

2024-04-15 | E-MTAB-13477 | biostudies-arrayexpress

GTF2I dosage regulates neuronal differentiation and social behavior in 7q11.23 neurodevelopmental disorders Organoid SC

ORGANISM(S): Homo sapiens

2024-06-27 | E-MTAB-13478 | biostudies-arrayexpress

GTF2I dosage regulates neuronal differentiation and social behavior in 7q11.23 neurodevelopmental disorders Mice

Mice experiment for GTF2I dosage regulates neuronal differentiation and social behavior in 7q11.23 neurodevelopmental disorders

ORGANISM(S): Mus musculus

2024-03-28 | E-MTAB-13475 | biostudies-arrayexpress