Neurodevelopmental disease

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Unknown (3528)
Genomics (450)
Transcriptomics (347)
Proteomics (82)
Metabolomics (17)
Methylation profiling (14)
Genomic (13)
Other (10)

Organisms

Homo sapiens (311)
Mus musculus (137)
Andropogon gerardi (58)
Bacteria (58)
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Canis lupus familiaris (58)
Clavibacter nebraskensis NCPPB 2581 (58)
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Ensifer adhaerens (58)
Halictus scabiosae (58)
Human alphaherpesvirus 1 strain 17 (58)
Human alphaherpesvirus 1 strain KOS (58)
Human betaherpesvirus 5 (58)
Human herpesvirus 2 strain 186 (58)
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synthetic construct (1)
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Organisms

Homo sapiens (190)
Mus musculus (82)
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gut metagenome (1)
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Repository

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geo (270)
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pride (58)
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Tissue

Cell culture (20)
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Blood (4)
Whole body (4)
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Blood cell (2)
Cerebral cortex neuron (2)
Neural cell (2)
Neuronal stem cell (2)
Pluripotent stem cell (2)
Stem cell (2)
Amniotic fluid (1)
Astrocyte (1)
Astrocyte of the cerebral cortex (1)
Blood plasma (1)
Capillary endothelial cell (1)
Cerebellar neuron (1)
Cerebral cortex pyramidal neuron (1)
Embryonic stem cell (1)
Excitatory neuron (1)
Gastrocnemius (1)
Generation of neurons (1)
Glutamatergic neuron (1)
Hippocampus (1)
Keratinocyte (1)
Leukocyte (1)
Microglial cell line (1)
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T cell (1)

Disease

Schizophrenia (4)
Disease free (3)
Rett syndrome (2)
Neurodevelopmental delay (2)
Cockayne syndrome (1)
Spinal muscular atrophy (1)
Parkinson's disease (1)
Arthrogryposis multiplex congenita-1 (1)
Autism spectrum disorder (1)
Congenital disorder of glycosylation (1)
Fetal akinesia deformation sequence syndrome (1)
Fragile X syndrome (1)
Genetic disease (1)
Hematopoietic system disease (1)
Human cytomegalovirus infection (1)
Kabuki syndrome (1)
Leigh disease (1)
Neurodegenerative disease (1)
Neurological dysfunction (1)
Obesity (1)
Periventricular nodular heterotopia (1)
Progressive myoclonus epilepsy 1A (1)
Respiratory failure (1)
Severe congenital neutropenia (1)
Syndromic intellectual disability (1)
Tonne-Kalscheuer syndrome (1)

Technology Type

Mass Spectrometry (58)
Shotgun proteomics (29)
Illumina HiSeq 2000 (18)
Bottom-up proteomics (11)
Mass spectrometry (9)
Mass spectrometry assay (8)
Data-dependent acquisition (8)
Illumina Genome Analyzer II, Illumina HiSeq 2000 (6)
HDMSE (6)
Data-independent acquisition (5)
Top-down proteomics (3)
Illumina HiSeq 2000, Illumina Genome Analyzer II (2)
Affinity proteomics (2)
Affinity purification coupled with mass spectrometry proteomics (2)
Gel-based experiment (2)
SWATH MS (2)
Illumina HiSeq 2000, Illumina HiSeq 2000 (ILLUMINA) (1)
Illumina HiSeq 2000, ILLUMINA (1)
NMR spectroscopy (1)
All-ion fragmentation (1)
DiaPASEF (1)
PAcIFIC (1)
SRM/MRM (1)
SomaScan affinity proteomics (1)

Instrument Platform

Illumina NovaSeq 6000 (14)
Orbitrap Fusion Lumos (6)
Liquid Chromatography MS - positive - reverse phase (6)
Illumina HiSeq 2500 (4)
Orbitrap Fusion (4)
Liquid Chromatography MS - positive - reverse-phase (4)
NextSeq 500 (3)
Illumina HiSeq 2000 (3)
Orbitrap Exploris 480 (3)
Q Exactive HF (3)
NextSeq 2000 (2)
LTQ Orbitrap Elite (2)
TimsTOF fleX (2)
Illumina NOVAseq 6000 (1)
IEO HPC (1)
Cutadapt, STAR (1)
TruSeq Stranded mRNA Sample Prep Kit (Illumina) (1)
BD InFlux Cytometer (Becton-Dickinson) (1)
Illumina NovaSeq X (1)
None (1)
R (1)
Illumina MiSeq (1)
Illumina HiSeq 1500 (1)
NextSeq 550 (1)
Illumina HiSeq 4000 (1)
Fusion Lumos Tribrid (1)
Q Exactive HF-X (1)
Q-Exactive Plus (1)
TripleTOF 5600 (1)
TripleTOF 6600 (1)

Publication Date

2026 (72)
2024 (69)
2025 (68)
2023 (45)
2022 (29)
2014 (28)
2011 (28)
2020 (26)
2018 (20)
2021 (19)
2016 (19)
2015 (19)
2013 (19)
2019 (14)
2010 (13)
2012 (12)
2017 (9)
2008 (5)
2007 (4)
2009 (2)
2006 (1)

CHEBI ID

CHEBI:16811 (3)
CHEBI:28842 (3)
CHEBI:28790 (3)
CHEBI:17154 (3)
CHEBI:16196 (3)
CHEBI:15843 (3)
CHEBI:36005 (3)
CHEBI:16704 (3)
CHEBI:16414 (3)
CHEBI:15354 (3)
CHEBI:17368 (3)
CHEBI:16747 (2)
CHEBI:18139 (2)
CHEBI:28941 (2)
CHEBI:28822 (2)
CHEBI:18101 (2)
CHEBI:77761 (2)
CHEBI:17822 (2)
CHEBI:26271 (2)
CHEBI:25094 (2)
CHEBI:18237 (2)
CHEBI:18186 (2)
CHEBI:43580 (2)
CHEBI:1427 (2)
CHEBI:28867 (2)
CHEBI:16750 (2)
CHEBI:16934 (2)
CHEBI:28875 (2)
CHEBI:15428 (2)
CHEBI:28631 (2)

Metabolite Name

PE 38:5 (3)
PE 38:3 (3)
7-Methylguanine (3)
Alanine (3)
Hypoxanthine (3)
PE 36:0 (2)
FA 10:0 (2)
PE 42:4 (2)
PE 37:1 (2)
PE 35:0 (2)
PE 36:4|PE 16:0_20:4 (2)
PE 38:6|PE 16:0_22:6 (2)
Val Glu Leu (2)
PC 44:6 (2)
PC 38:4|PC 18:0_20:4 (2)
PC 30:3 (2)
Val Val (2)
PC 35:0 (2)
PE 38:1 (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)

First Public Date

2025 (70)
2024 (63)
2026 (52)
2023 (29)
2020 (25)
2014 (23)
2022 (16)
2017 (13)
2019 (12)
2018 (11)
2021 (10)
2016 (9)
2013 (8)
2015 (1)

Modification

Not available (1)

Study type

Transcription profiling by array (68)
RNA-seq of coding RNA (35)
ChIP-seq (11)
Methylation profiling by array (11)
Comparative genomic hybridization by array (7)
Methylation profiling by high throughput sequencing (3)
Cell line - High-throughput sequencing (2)
DNA-seq (2)
RNA-seq of coding RNA from single cells (2)
Human - High-throughput sequencing (1)
Human - One-color microarray (1)
Animal - High-throughput sequencing (1)
Transcription profiling by tiling array (1)
Capture-C (1)
CLIP-seq (1)
Transcription profiling by RT-PCR (1)
MicroRNA profiling by high throughput sequencing (1)
ATAC-seq (1)
RIP-seq (1)
RNA-seq of non coding RNA (1)

Release Date

2025 (461)
2022 (459)
2023 (442)
2024 (407)
2021 (373)
2020 (260)
2019 (223)
2018 (185)
2017 (185)
2016 (130)
2015 (127)
2014 (123)
2013 (71)
2026 (63)
2011 (51)
2012 (44)
2010 (31)
2009 (15)
2008 (12)
2007 (6)
2006 (3)
2005 (3)
2004 (2)
2003 (2)
2002 (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)
Lab of Neuroproteomics, Department of Biochemistry and Tissue Biology, Institute of Biology, University of Campinas (UNICAMP), Campinas, SP, Brazil (4)
1)Neurometabolic Diseases Laboratory, Bellvitge Biomedical Research Institute (IDIBELL), L’Hospitalet de Llobregat, Barcelona, Catalonia, Spain 2) Centre for Biomedical Research on Rare Diseases (CIBERER), Instituto de Salud Carlos III, Madrid, Spain 3)Catalan Institution of Research and Advanced Studies (ICREA), Barcelona, Catalonia, Spain (1)
95 Institut de Pharmacologie et de Biologie Structurale (IPBS), Université de Toulouse, CNRS, Université Toulouse III - Paul Sabatier (UT3), Toulouse, 31077, France (1)
Associate Professor Virginia Tech (1)
Associate Professor, Immunobiology Associate Research Scientist, A2DRC The University of Arizona, USA (1)
Baker Heart and Diabetes Institute (1)
Biomedical Neuroscience Institute, Faculty of Medicine, University of Chile, Santiago, Chile. Center for Geroscience, Brain Health and Metabolism, Santiago, Chile. Program of Cellular and Molecular Biology, Center for Molecular Studies of the Cell, Institute of Biomedical Sciences, University of Chile, Santiago, Chile. (1)
Biomolecular Mass Spectrometry and Proteomics, Bijvoet Center for Biomolecular Research and Utrecht Institute for Pharmaceutical Sciences, University of Utrecht, Padualaan 8, 3584 CH Utrecht, the Netherlands. (1)
CCB, LUMC, Netherlands (1)
Cancer Sciences Faculty of Medicine University of Southampton (1)
Chiara Guerrera, IRHC, HDR Head of the Necker Proteomics Faculty of Medecine, University Paris Cité SFR Necker INSERM US24 160 rue de Vaugirard | 75015 Paris Tél. 01 40 61 54 6 (1)
Department of Biological Sciences The University of Texas at El Paso US (1)
Department of Biological Sciences, Korea Advanced Institute for Science and Technology (KAIST), Korea (1)
Department of Biology, University of Ottawa, Ottawa, Canada, K1N 6N5 (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)
Department of General Pediatrics, Neonatology and Pediatric Cardiology, Heinrich Heine University, Duesseldorf, Germany (1)
Department of General Pediatrics, Neonatology and Pediatric Cardiology, Heinrich Heine University, Medical Faculty, Düsseldorf, Germany (1)
Department of Laboratory Medicine and Pathology Mayo Clinic, Rochester, Minnesota 55905 United States (1)
Department of Laboratory Medicine, Wiita Lab, University of California, San Francisco, USA (1)
Department of Neuroscience, Intellectual and Developmental Disabilities Research Center, Washington University School of Medicine, St. Louis, MO, 63110, USA (1)
Department of Physiological Genomics, Biomedical Center, Ludwig-Maximilians University, Germany (1)
Department of Structural and Molecular Biology IBMB-CSIC Barcelona, Spain (1)
Developmental Neurobiology, Max Planck Institute of Psychiatry, Munich, Germany (1)
Division of Systems Medicine, Imperial College London (1)
Fondazione Human Technopole (1)
IRCCS Istituto G Gaslini (1)
Keck MS & Proteomics Resource at Yale University Dept. MBB, Yale University (1)
Kids Neuroscience Centre, The Children's Hospital at Westmead, Faculty of Medicine and Health, University of Sydney (1)
Laboratory of Genome Dynamics, Institute of Molecular Genetics of the Czech Academy of Sciences, Prague 4, 142 20, Czech Republic (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

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

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

Transcriptomics integrated with metabolomics reveals partial molecular mechanisms of nutritional risk and neurodevelopment in children with congenital heart disease

PURPOSE: To explore molecular mechanisms affecting nutritional risk and neurodevelopment in children with congenital heart disease (CHD) by combining transcriptome and metabolome analysis.

METHODS: A total of 26 blood and serum samples from 3 groups of chil...

2024-10-25 | MTBLS10118 | MetaboLights

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

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

MeCP2 links heterochromatin condensates and neurodevelopmental disease

PRJNA578117 | ENA

Neurodevelopmental and behavioral defects in congenital heart disease [methylation]

PRJNA1194225 | ENA

Title: Neurodevelopmental and behavioral defects in congenital heart disease

PRJNA1194224 | ENA