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Search life-sciences literature (45,104,145 articles, preprints and more)

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Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes.
Epi25 Collaborative
Nat Neurosci, 27(10):1864-1879, 03 Oct 2024
Cited by: 0 articles | PMID: 39363051
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Analysis of single-cell transcriptome data from a mouse model implicates protein synthesis dysfunction in schizophrenia.
Weller AE, Ferraro TN, Doyle GA, Reiner BC, Berrettini WH, Crist RC
Genes Genomics, 46(9):1071-1084, 31 Jul 2024
Cited by: 0 articles | PMID: 39083157
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An exploratory metabolomic comparison of participants with fast or absent functional progression from 2CARE, a randomized, double-blind clinical trial in Huntington's disease.
McGarry A, Hunter K, Gaughan J, Auinger P, Ferraro TN, Pradhan B, Ferrucci L, Egan JM, Moaddel R
Sci Rep, 14(1):1101, 11 Jan 2024
Cited by: 1 article | PMID: 38212353 | PMCID: PMC10784537
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Postmortem toxicology findings from the Camden Opioid Research Initiative.
Kusic DM, Heil J, Zajic S, Brangan A, Dairo O, Heil S, Feigin G, Kacinko S, Buono RJ, Ferraro TN, Rafeq R, Haroz R, Baston K, Bodofsky E, Sabia M, Salzman M, Resch A, Madzo J, Scheinfeldt LB, [...] Jelinek J
PLoS One, 18(11):e0292674, 01 Nov 2023
Cited by: 1 article | PMID: 37910493 | PMCID: PMC10619848
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GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture.
International League Against Epilepsy Consortium on Complex Epilepsies
Nat Genet, 55(9):1471-1482, 31 Aug 2023
Cited by: 32 articles | PMID: 37653029 | PMCID: PMC10484785
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Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals.
Montanucci L, Lewis-Smith D, Collins RL, Niestroj LM, Parthasarathy S, Xian J, Ganesan S, Macnee M, Brünger T, Thomas RH, Talkowski M, Epi25 Collaborative, Helbig I, Leu C, Lal D
Nat Commun, 14(1):4392, 20 Jul 2023
Cited by: 8 articles | PMID: 37474567 | PMCID: PMC10359300
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Decoding brain memory formation by single-cell RNA sequencing.
Sardoo AM, Zhang S, Ferraro TN, Keck TM, Chen Y
Brief Bioinform, 23(6):bbac412, 01 Nov 2022
Cited by: 6 articles | PMID: 36156112 | PMCID: PMC9677489
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Single nucleus transcriptomic analysis of rat nucleus accumbens reveals cell type-specific patterns of gene expression associated with volitional morphine intake.
Reiner BC, Zhang Y, Stein LM, Perea ED, Arauco-Shapiro G, Ben Nathan J, Ragnini K, Hayes MR, Ferraro TN, Berrettini WH, Schmidt HD, Crist RC
Transl Psychiatry, 12(1):374, 08 Sep 2022
Cited by: 18 articles | PMID: 36075888 | PMCID: PMC9458645
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Patient Perceptions and Potential Utility of Pharmacogenetic Testing in Chronic Pain Management and Opioid Use Disorder in the Camden Opioid Research Initiative.
Kusic D, Heil J, Zajic S, Brangan A, Dairo O, Smith G, Morales-Scheihing D, Buono RJ, Ferraro TN, Haroz R, Salzman M, Baston K, Bodofsky E, Sabia M, Resch A, Scheinfeldt LB
Pharmaceutics, 14(9):1863, 03 Sep 2022
Cited by: 2 articles | PMID: 36145611 | PMCID: PMC9505214
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Single Nucleus Transcriptome Data from Alzheimer's Disease Mouse Models Yield New Insight into Pathophysiology.
Weller AE, Ferraro TN, Doyle GA, Reiner BC, Crist RC, Berrettini WH
J Alzheimers Dis, 90(3):1233-1247, 01 Jan 2022
Cited by: 7 articles | PMID: 36213995
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Consensus clustering of single-cell RNA-seq data by enhancing network affinity.
Cui Y, Zhang S, Liang Y, Wang X, Ferraro TN, Chen Y
Brief Bioinform, 22(6):bbab236, 01 Nov 2021
Cited by: 11 articles | PMID: 34160582 | PMCID: PMC8574980
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Genetics and prescription opioid use (GaPO): study design for consenting a cohort from an existing biobank to identify clinical and genetic factors influencing prescription opioid use and abuse.
Troiani V, Crist RC, Doyle GA, Ferraro TN, Beiler D, Ranck S, McBryan K, Jarvis MA, Barbour JS, Han JJ, Ness RJ, Berrettini WH, Robishaw JD
BMC Med Genomics, 14(1):253, 26 Oct 2021
Cited by: 4 articles | PMID: 34702274 | PMCID: PMC8547564
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Distinct gene-set burden patterns underlie common generalized and focal epilepsies.
Koko M, Krause R, Sander T, Bobbili DR, Nothnagel M, May P, Lerche H, Epi25 Collaborative
EBioMedicine, 72:103588, 24 Sep 2021
Cited by: 8 articles | PMID: 34571366 | PMCID: PMC8479647
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Genetic Variation in PADI6-PADI4 on 1p36.13 Is Associated with Common Forms of Human Generalized Epilepsy.
Buono RJ, Bradfield JP, Wei Z, Sperling MR, Dlugos DJ, Privitera MD, French JA, Lo W, Cossette P, Schachter SC, Basehore H, Lohoff FW, Grant SFA, Ferraro TN, Hakonarson H
Genes (Basel), 12(9):1441, 18 Sep 2021
Cited by: 3 articles | PMID: 34573423 | PMCID: PMC8472138
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Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals.
Epi25 Collaborative. Electronic address: [email protected], Epi25 Collaborative
Am J Hum Genet, 108(10):2024, 01 Oct 2021
Cited by: 0 articles | PMID: 34626584 | PMCID: PMC8546036
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Effectiveness of a Team-Based Learning exercise in the learning outcomes of a medical pharmacology course: insight from struggling students.
Carrasco GA, Behling KC, Gentile M, Fischer BD, Ferraro TN
Naunyn Schmiedebergs Arch Pharmacol, 394(9):1941-1948, 07 Jun 2021
Cited by: 2 articles | PMID: 34097095
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Shared genetic basis between genetic generalized epilepsy and background electroencephalographic oscillations.
Stevelink R, Luykx JJ, Lin BD, Leu C, Lal D, Smith AW, Schijven D, Carpay JA, Rademaker K, Rodrigues Baldez RA, Devinsky O, Braun KPJ, Jansen FE, Smit DJA, Koeleman BPC, International League Against Epilepsy Consortium on Complex Epilepsies, Epi25 Collaborative
Epilepsia, 62(7):1518-1527, 18 May 2021
Cited by: 3 articles | PMID: 34002374 | PMCID: PMC8672363
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Investigation of long interspersed element-1 retrotransposons as potential risk factors for idiopathic temporal lobe epilepsy.
Doyle GA, Reiner BC, Crist RC, Rao AM, Ojeah NS, Arauco-Shapiro G, Levinson RN, Shah LD, Sperling MR, Ferraro TN, Buono RJ, Berrettini WH
Epilepsia, 62(6):1329-1342, 07 Apr 2021
Cited by: 4 articles | PMID: 33826137
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Author Correction: Cross-sectional analysis of plasma and CSF metabolomic markers in Huntington's disease for participants of varying functional disability: a pilot study.
McGarry A, Gaughan J, Hackmyer C, Lovett J, Khadeer M, Shaikh H, Pradhan B, Ferraro TN, Wainer IW, Moaddel R
Sci Rep, 11(1):9947, 05 May 2021
Cited by: 0 articles | PMID: 33953296 | PMCID: PMC8100122
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Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals.
Epi25 Collaborative. Electronic address: [email protected], Epi25 Collaborative
Am J Hum Genet, 108(6):965-982, 30 Apr 2021
Cited by: 22 articles | PMID: 33932343 | PMCID: PMC8206159
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The Genomics of Opioid Addiction Longitudinal Study (GOALS): study design for a prospective evaluation of genetic and non-genetic factors for development of and recovery from opioid use disorder.
Heil J, Zajic S, Albertson E, Brangan A, Jones I, Roberts W, Sabia M, Bodofsky E, Resch A, Rafeq R, Haroz R, Buono R, Ferraro TN, Scheinfeldt L, Salzman M, Baston K
BMC Med Genomics, 14(1):16, 07 Jan 2021
Cited by: 3 articles | PMID: 33413350 | PMCID: PMC7792024
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Cross-sectional analysis of plasma and CSF metabolomic markers in Huntington's disease for participants of varying functional disability: a pilot study.
McGarry A, Gaughan J, Hackmyer C, Lovett J, Khadeer M, Shaikh H, Pradhan B, Ferraro TN, Wainer IW, Moaddel R
Sci Rep, 10(1):20490, 24 Nov 2020
Cited by: 16 articles | PMID: 33235276 | PMCID: PMC7686309
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Single-nuclei transcriptomics of schizophrenia prefrontal cortex primarily implicates neuronal subtypes
Reiner BC, Crist RC, Stein LM, Weller AE, Doyle GA, Arauco-Shapiro G, Turecki G, Ferraro TN, Hayes MR, Berrettini WH
bioRxiv, 29 Jul 2020
Cited by: 0 articles | PPR: PPR193913
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Assessment of Probable Opioid Use Disorder Using Electronic Health Record Documentation.
Palumbo SA, Adamson KM, Krishnamurthy S, Manoharan S, Beiler D, Seiwell A, Young C, Metpally R, Crist RC, Doyle GA, Ferraro TN, Li M, Berrettini WH, Robishaw JD, Troiani V
JAMA Netw Open, 3(9):e2015909, 01 Sep 2020
Cited by: 33 articles | PMID: 32886123 | PMCID: PMC7489858
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The Molecular Genetic Interaction Between Circadian Rhythms and Susceptibility to Seizures and Epilepsy.
Re CJ, Batterman AI, Gerstner JR, Buono RJ, Ferraro TN
Front Neurol, 11:520, 23 Jun 2020
Cited by: 8 articles | PMID: 32714261 | PMCID: PMC7344275
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1-25 of 156 results

1 2 3 Next ...

Search life-sciences literature (45,104,145 articles, preprints and more)

Search results

Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes.

Analysis of single-cell transcriptome data from a mouse model implicates protein synthesis dysfunction in schizophrenia.

An exploratory metabolomic comparison of participants with fast or absent functional progression from 2CARE, a randomized, double-blind clinical trial in Huntington's disease.

Postmortem toxicology findings from the Camden Opioid Research Initiative.

GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture.

Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals.

Decoding brain memory formation by single-cell RNA sequencing.

Single nucleus transcriptomic analysis of rat nucleus accumbens reveals cell type-specific patterns of gene expression associated with volitional morphine intake.

Patient Perceptions and Potential Utility of Pharmacogenetic Testing in Chronic Pain Management and Opioid Use Disorder in the Camden Opioid Research Initiative.

Single Nucleus Transcriptome Data from Alzheimer's Disease Mouse Models Yield New Insight into Pathophysiology.

Consensus clustering of single-cell RNA-seq data by enhancing network affinity.

Genetics and prescription opioid use (GaPO): study design for consenting a cohort from an existing biobank to identify clinical and genetic factors influencing prescription opioid use and abuse.

Distinct gene-set burden patterns underlie common generalized and focal epilepsies.

Genetic Variation in PADI6-PADI4 on 1p36.13 Is Associated with Common Forms of Human Generalized Epilepsy.

Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals.

Effectiveness of a Team-Based Learning exercise in the learning outcomes of a medical pharmacology course: insight from struggling students.

Shared genetic basis between genetic generalized epilepsy and background electroencephalographic oscillations.

Investigation of long interspersed element-1 retrotransposons as potential risk factors for idiopathic temporal lobe epilepsy.

Author Correction: Cross-sectional analysis of plasma and CSF metabolomic markers in Huntington's disease for participants of varying functional disability: a pilot study.

Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals.

The Genomics of Opioid Addiction Longitudinal Study (GOALS): study design for a prospective evaluation of genetic and non-genetic factors for development of and recovery from opioid use disorder.

Cross-sectional analysis of plasma and CSF metabolomic markers in Huntington's disease for participants of varying functional disability: a pilot study.

Single-nuclei transcriptomics of schizophrenia prefrontal cortex primarily implicates neuronal subtypes

Assessment of Probable Opioid Use Disorder Using Electronic Health Record Documentation.

The Molecular Genetic Interaction Between Circadian Rhythms and Susceptibility to Seizures and Epilepsy.

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