1
Long COVID-19 and Peripheral Serotonin: A Commentary and Reconsideration

von Anderson GM ; Cook EH ; Blakely RD ; et al.

Journal of Inflammation Research, Vol 17, Pp 2169-2172 (2024)

Schlagworte: serotonin; covid-19; plasma; platelets; long-covid; viral infection; Pathology; RB1-214; Therapeutics. Pharmacology; RM1-950
- Zum Volltext in DOAJ
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2
Point-cloud based machine learning for classifying rare events in the Active-Target Time Projection Chamber

von Dey, Poulomi ; Anthony, Adam K. ; Hunt, Curtis ; et al.

In Nuclear Inst. and Methods in Physics Research, A March 2025 1072
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3
No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer

von Hollestelle, Antoinette ; van der Baan, Frederieke H. ; Berchuck, Andrew ; et al.

In Gynecologic Oncology May 2016 141(2):386-401
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4
Genome-wide association study of pediatric obsessive-compulsive traits: shared genetic risk between traits and disorder

von Burton, CL ; Lemire, M ; Xiao, B ; et al.

urn:ISSN:2158-3188 ; Translational Psychiatry, 11, 1, 91

Schlagworte: 32 Biomedical and Clinical Sciences; 5202 Biological Psychology; 3202 Clinical Sciences; 3209 Neurosciences; 52 Psychology; Prevention; Genetics; Pediatric Research Initiative; Human Genome; Mental Health; Mental Illness; Brain Disorders; Anxiety Disorders; Serious Mental Illness; Adolescent; Child; Compulsive Behavior; Genome-Wide Association Study; Humans; Obsessive-Compulsive Disorder; Phenotype; Risk Factors; OCD Working Group of the Psychiatric Genomics Consortium; anzsrc-for: 32 Biomedical and Clinical Sciences; anzsrc-for: 5202 Biological Psychology; anzsrc-for: 3202 Clinical Sciences; anzsrc-for: 3209 Neurosciences; anzsrc-for: 52 Psychology; anzsrc-for: 1103 Clinical Sciences; anzsrc-for: 1117 Public Health and Health Services
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5
A framework for an evidence-based gene list relevant to autism spectrum disorder

von Schaaf, CP ; Betancur, C ; Yuen, RKC ; et al.

Nature Reviews Genetics , 21 (6) pp. 367-376. (2020)
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6
Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders

von Lee, PH ; Anttila, V ; Won, H ; et al.

Cell , 179 (7) 1469-1482.e11. (2019)

Schlagworte: Science & Technology; Life Sciences & Biomedicine; Biochemistry & Molecular Biology; Cell Biology; WIDE ASSOCIATION; HUMAN BRAIN; GENETIC CORRELATIONS; GENOTYPE IMPUTATION; INSIGHTS; IDENTIFICATION; TRANSCRIPTOME; DEMETHYLASE; MUTATIONS; DISEASES
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7
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

von Fu JM ; Satterstrom FK ; Peng M ; et al.

Schlagworte: Autism spectrum disorders; Gene expression; Genetic association study; Neurodevelopmental disorders
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8
Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia

von Anney RJL ; Ripke S ; Anttila V ; et al.

Molecular Autism, 22 May 2017
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9
Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia

von Anney, RJL ; Ripke, S ; Anttila, V ; et al.
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10
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

von Weiner, DJ ; Wigdor, EM ; Ripke, S ; et al.

Nature Genetics , 49 (7) pp. 978-985. (2017)

Schlagworte: Science & Technology; Life Sciences & Biomedicine; Genetics & Heredity; GENOME-WIDE ASSOCIATION; SIMONS SIMPLEX COLLECTION; GENETIC RISK; DE-NOVO; GENERAL-POPULATION; VARIANTS; MUTATIONS; INSIGHTS; DISEASE; BIOLOGY
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11
Cross-Disorder Genome-Wide Analyses Suggest a Complex Genetic Relationship Between Tourette's Syndrome and OCD

von Yu, DM ; Mathews, CA ; Scharf, JM ; et al.

Yu, DM, Mathews, CA, Scharf, JM, Neale, BM, Davis, LK, Gamazon, ER, Derks, EM, Evans, P, Edlund, CK, Crane, J, Osiecki, L, Gallagher, P, Gerber, G, Haddad, S, Illmann, C, McGrath, LM, Mayerfeld, C, Arepalli, S, Barlassina, C, Barr, CL, Bellodi, L, Benarroch, F, Berrio, GB, Bienvenu, OJ, Black, DW, Bloch, MH, Brentani, H, Bruun, RD, Budman, CL, Camarena, B, Campbell, DD, Cappi, C, Silgado, JCC, Cavallini, MC, Chavira, DA, Chouinard, S, Cook, EH, Cookson, MR, Coric, V, Cullen, B, Cusi, D, Delorme, R, Denys, D, Dion, Y, Eapen, V, Egberts, K, Falkai, P, Fernandez, T, Fournier, E, Garrido, ....

Schlagworte: /dk/atira/pure/keywords/researchprograms/AFL001000/EMCMGC029601; name=EMC MGC-02-96-01; /dk/atira/pure/keywords/researchprograms/AFL001000/EMCNIHES045501; name=EMC NIHES-04-55-01
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12
A genome-wide association study of autism using the Simons simplex collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?

von Chaste, P ; Klei, L ; Sanders, SJ ; et al.

Biological Psychiatry, vol 77, iss 9

Schlagworte: Psychiatry; Biological Sciences; Medical and Health Sciences; Psychology and Cognitive Sciences
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13
The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism

von Hadley D ; Wu Z-L ; Kao C ; et al.

Nature Communications, 13 June 2014
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14
Partitioning the Heritability of Tourette Syndrome and Obsessive Compulsive Disorder Reveals Differences in Genetic Architecture

von Davis, LK ; Yu, DM ; Keenan, CL ; et al.

Davis, LK, Yu, DM, Keenan, CL, Gamazon, ER, Konkashbaev, AI, Derks, EM, Neale, BM, Yang, J, Lee, SH, Evans, P, Barr, CL, Bellodi, L, Benarroch, F, Berrio, GB, Bienvenu, OJ, Bloch, MH, Blom, RM, Bruun, RD, Budman, CL, Camarena, B, Campbell, D, Cappi, C, Silgado, JCC, Cath, DC, Cavallini, MC, Chavira, DA, Chouinard, S, Conti, DV, Cook, EH, Coric, V, Cullen, BA, Deforce, D, Delorme, R, Dion, Y, Edlund, CK, Egberts, K, Falkai, P, Fernandez, TV, Gallagher, PJ, Garrido, H, Geller, D, Girard, SL, Grabe, HJ, Grados, MA, Greenberg, BD, Gross-Tsur, V, Haddad, S, Heiman, GA, Hemmings, SMJ, Hounie, ....

Schlagworte: /dk/atira/pure/keywords/researchprograms/AFL001000/EMCMGC029601; name=EMC MGC-02-96-01; /dk/atira/pure/keywords/researchprograms/AFL001000/EMCNIHES045501; name=EMC NIHES-04-55-01
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15
Genome-wide association study of obsessive-compulsive disorder

von Stewart, SE ; Yu, D ; Scharf, JM ; et al.

MOLECULAR PSYCHIATRY ; ISSN: 1359-4184

Schlagworte: Biology and Life Sciences; DLGAP; genetic; genomic; GWAS; neurodevelopmental disorder; obsessive-compulsive disorder; OCD COLLABORATIVE GENETICS; FAMILY-BASED ASSOCIATION; QUANTITATIVE TRAIT LOCI; TRANSPORTER GENE; LINKAGE; SLC1A1; SNPS; TWIN; REPLICATION; EXPRESSION
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16
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

von Lee, SH ; Ripke, S ; Neale, BM ; et al.

NATURE GENETICS ; ISSN: 1061-4036

Schlagworte: Social Sciences; MAJOR DEPRESSIVE DISORDER; AUTISM SPECTRUM DISORDERS; DEFICIT HYPERACTIVITY DISORDER; ATTENTION-DEFICIT/HYPERACTIVITY DISORDER; COMMON SNPS; BIPOLAR DISORDER; CROHNS-DISEASE; SCHIZOPHRENIA; RISK; ASSOCIATION
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17
~stantSecretary for Environmental Management Enclosures cc w/o Enclosures

von B. Cook Eh-l ; S. Cary Eh-l ; M. Whitaker S ; et al.

http://www.dnfsb.gov/sites/default/files/Board Activities/Letters/2002/ltr_2002328_9026.pdf.

Schlagworte: Team Members Approval
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18
T594M and G442V polymorphisms of the sodium channel β subunit and hypertension in a black population

von Dong, YB ; Zhu, HD ; Baker, EH ; et al.

Journal of Human Hypertension. 15(6):425-430
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19
Autism and the serotonin transporter: the long and short of it

von Devlin, B ; Cook, EH ; Coon, H ; et al.

Molecular Psychiatry, vol 10, iss 12

Schlagworte: Pharmacology and Pharmaceutical Sciences; Biomedical and Clinical Sciences; Brain Disorders; Mental Health; Pediatric; Behavioral and Social Science; Autism; Intellectual and Developmental Disabilities (IDD); Neurosciences; Genetics; 2.1 Biological and endogenous factors; Adult; Autistic Disorder; Child; Gene Frequency; Genetic Predisposition to Disease; Humans; Linkage Disequilibrium; Minisatellite Repeats; Pedigree; Phenotype; Polymorphism; Genetic; Serotonin Plasma Membrane Transport Proteins; serotonin transporter; heterogeneity; genetic association; CPEA Genetics Network; protein; unclassified drug
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20
Mutation screening of the UBE3A/E6-AP gene in autistic disorder

von Veenstra-VanderWeele, J ; Gonen, D ; Leventhal, B L ; et al.

Molecular Psychiatry. 4(1):64-67
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21
Evidence of linkage between the serotonin transporter and autistic disorder

von Jr, EH Cook ; Courchesne, R ; Lord, C ; et al.

Molecular Psychiatry. 2(3):247-250
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22
Contemporary Ventilation Strategies And Adjunctive Therapies For Acute Respiratory Distress Syndrome (Ards)

von Duan, EH ; Adhikari, NK ; Hand, L ; et al.

Intensive Care Medicine Experimental. December 2015 3(1):1-2
- Zum Volltext in PubMed Central
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23
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

von Sattterstrom, FK ; Kosmicki, JA ; Wang, J ; et al.

Schlagworte: autism spectrum disorder; cell type; cytoskeleton; excitatory neurons; excitatory-inhibitory balance
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24
Mutation screening of human 5-HT2Breceptor gene in early-onset obsessive-compulsive disorder

von Kim, S-J ; Veenstra-VanderWeele, J ; Hanna, GL ; et al.

In Molecular and Cellular Probes February 2000 14(1):47-52
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25
A genome-wide linkage and association scan reveals novel loci for autism.

von WEISS LA, ARKING DE ; GENE DISCOVERY PROJECT OF JOHNS HOPKINS ; THE AUTISM CONSORTIUM ; et al.
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