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Showing 401–450 of 450 results

Advanced filters: Author: Mark D Wheeler Clear advanced filters

Reversal of Startle Gating Deficits in Transgenic Mice Overexpressing Corticotropin-Releasing Factor by Antipsychotic Drugs

Anneloes Dirks
Lucianne Groenink
Berend Olivier
Research03 Jun 2003
Neuropsychopharmacology

Volume: 28, P: 1790-1798
Visiting nature is associated with lower socioeconomic inequalities in well-being in Wales

Joanne K. Garrett
Francis M. Rowney
Benedict W. Wheeler
ResearchOpen Access15 Jun 2023
Scientific Reports

Volume: 13, P: 1-13
Alterations in the BOLD fMRI signal with ageing and disease: a challenge for neuroimaging

Mark D'Esposito
Leon Y. Deouell
Adam Gazzaley
Reviews01 Nov 2003
Nature Reviews Neuroscience

Volume: 4, P: 863-872
Identification of circulating proteins associated with general cognitive function among middle-aged and older adults

Analysis of circulating proteins across multiple cohorts identifies proteins that are associated with cognitive function and may serve as targets to understand the relationship between immunity and Alzheimer’s disease risk.

Adrienne Tin
Alison E. Fohner
Myriam Fornage
ResearchOpen Access03 Nov 2023
Communications Biology

Volume: 6, P: 1-14
The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities

A comparison of the frequency of pathogenic mutations in 73 genes in the All of Us cohort highlights the differences in pathogenic variation attributed to ancestry.

Eric Venner
Karynne Patterson
Miriam Vos
ResearchOpen Access19 Feb 2024
Communications Biology

Volume: 7, P: 1-11
Effect of cardiometabolic risk factors on the relationship between adiposity and bone mass in girls

Megan Hetherington-Rauth
Jennifer W. Bea
Scott B. Going
Research11 Jun 2018
International Journal of Obesity

Volume: 42, P: 1185-1194
Clinical sites of the Undiagnosed Diseases Network: unique contributions to genomic medicine and science

Kelly Schoch
Cecilia Esteves
Vandana Shashi
Research23 Oct 2020
Genetics in Medicine

Volume: 23, P: 259-271
Multigene methylation analysis of Wilms' tumour and adult renal cell carcinoma

Mark R Morris
Luke B Hesson
Eamonn R Maher
Research02 Oct 2003
Oncogene

Volume: 22, P: 6794-6801
Mendelian randomisation analysis strongly implicates adiposity with risk of developing colorectal cancer

David Jarvis
Jonathan S Mitchell
Richard S Houlston
ResearchOpen Access23 Jun 2016
British Journal of Cancer

Volume: 115, P: 266-272
Genome-wide association analysis of type 2 diabetes in the EPIC-InterAct study

Lina Cai
Eleanor Wheeler
Nicholas J. Wareham
ResearchOpen Access13 Nov 2020
Scientific Data

Volume: 7, P: 1-6
Bioengineered model of the human motor unit with physiologically functional neuromuscular junctions

Rowan P. Rimington
Jacob W. Fleming
Mark P. Lewis
ResearchOpen Access03 Jun 2021
Scientific Reports

Volume: 11, P: 1-15
Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes

Sonja I. Berndt
Joseph Vijai
Nathaniel Rothman
Research22 Oct 2022
Leukemia

Volume: 36, P: 2835-2844
Experimental demonstration of dynamic thermal regulation using vanadium dioxide thin films

Ahmed M. Morsy
Michael T. Barako
Michelle L. Povinelli
ResearchOpen Access18 Aug 2020
Scientific Reports

Volume: 10, P: 1-10
Cardioprotective effects of early versus late initiated antiretroviral treatment in adolescents with perinatal HIV-1 infection

Itai M. Magodoro
Carlos E. Guerrero-Chalela
Ntobeko A. B. Ntusi
ResearchOpen Access20 Jun 2024
Scientific Reports

Volume: 14, P: 1-10
New paradigms for understanding and step changes in treating active and chronic, persistent apicomplexan infections

Martin McPhillie
Ying Zhou
Rima McLeod
ResearchOpen Access14 Jul 2016
Scientific Reports

Volume: 6, P: 1-23
Is the rostro-caudal axis of the frontal lobe hierarchical?

Studies into the role of different frontal cortex areas in cognitive control have suggested that there is a rostral-to-caudal processing gradient. Drawing on anatomical and functional data from humans and monkeys, Badre and D'Esposito discuss whether this gradient might reflect a hierarchical organization.

David Badre
Mark D'Esposito
Reviews12 Aug 2009
Nature Reviews Neuroscience

Volume: 10, P: 659-669
COVID-19 due to the B.1.617.2 (Delta) variant compared to B.1.1.7 (Alpha) variant of SARS-CoV-2: a prospective observational cohort study

Kerstin Kläser
Erika Molteni
Emma L. Duncan
ResearchOpen Access28 Jun 2022
Scientific Reports

Volume: 12, P: 1-17
An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids

Sacha Ferdinandusse
Kirsty McWalter
Frédéric M. Vaz
ResearchOpen Access26 Nov 2020
Genetics in Medicine

Volume: 23, P: 740-750
DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract

Alexandria T. M. Blackburn
Nasim Bekheirnia
Mir Reza Bekheirnia
Research02 Jul 2019
Genetics in Medicine

Volume: 21, P: 2755-2764
Haploinsufficiency of PRR12 causes a spectrum of neurodevelopmental, eye, and multisystem abnormalities

Fuad Chowdhury
Lei Wang
Tugce B. Balci
Research06 Apr 2021
Genetics in Medicine

Volume: 23, P: 1234-1245
Publisher Correction: SARS-CoV-2 Omicron is an immune escape variant with an altered cell entry pathway

Brian J. Willett
Joe Grove
Emma C. Thomson
Amendments and CorrectionsOpen Access16 Sept 2022
Nature Microbiology

Volume: 7, P: 1709
Poorer aging trajectories are associated with elevated serotonin synthesis capacity

Teodora Z. Markova
Claire J. Ciampa
Anne S. Berry
Research17 Jul 2023
Molecular Psychiatry

Volume: 28, P: 4390-4398
DNA methylation patterns identify subgroups of pancreatic neuroendocrine tumors with clinical association

Lakis et al. report novel findings related to the epigenetic landscape of pancreatic neuroendocrine cancer. This relatively large cohort provides functional insights into the epigenetic wiring of pancreatic neuroendocrine tumor sub-types with the potential ability to stratify tumours of different prognosis.

Vanessa Lakis
Rita T. Lawlor
Aldo Scarpa
ResearchOpen Access03 Feb 2021
Communications Biology

Volume: 4, P: 1-11
Bi-allelic ATG4D variants are associated with a neurodevelopmental disorder characterized by speech and motor impairment

Marie Morimoto
Vikas Bhambhani
May Christine V. Malicdan
ResearchOpen Access10 Feb 2023
npj Genomic Medicine

Volume: 8, P: 1-16
Results from an 18 country cross-sectional study examining experiences of nature for people with common mental health disorders

Michelle Tester-Jones
Mathew P. White
Lora E. Fleming
ResearchOpen Access06 Nov 2020
Scientific Reports

Volume: 10, P: 1-11
Associations among locus coeruleus catecholamines, tau pathology, and memory in aging

Claire J. Ciampa
Jourdan H. Parent
Anne S. Berry
Research15 Jan 2022
Neuropsychopharmacology

Volume: 47, P: 1106-1113
Associations between green/blue spaces and mental health across 18 countries

Mathew P. White
Lewis R. Elliott
Lora E. Fleming
ResearchOpen Access26 Apr 2021
Scientific Reports

Volume: 11, P: 1-12
Connectivity to the surface determines diversity patterns in subsurface aquifers of the Fennoscandian shield

Valerie Hubalek
Xiaofen Wu
Danny Ionescu
ResearchOpen Access29 Mar 2016
The ISME Journal

Volume: 10, P: 2447-2458
Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11

Thomas A. Ravenscroft
Jennifer B. Phillips
Hugo J. Bellen
Research10 Jun 2021
Genetics in Medicine

Volume: 23, P: 1889-1900
Genomic epidemiology of SARS-CoV-2 in a university outbreak setting and implications for public health planning

Sema Nickbakhsh
Joseph Hughes
Alison Smith-Palmer
ResearchOpen Access19 Jul 2022
Scientific Reports

Volume: 12, P: 1-17
An analysis and evaluation of the WeFold collaborative for protein structure prediction and its pipelines in CASP11 and CASP12

Chen Keasar
Liam J. McGuffin
Silvia N. Crivelli
ResearchOpen Access02 Jul 2018
Scientific Reports

Volume: 8, P: 1-18
Next-generation carrier screening

Mark A. Umbarger
Caleb J. Kennedy
Gregory J. Porreca
ResearchOpen Access13 Jun 2013
Genetics in Medicine

Volume: 16, P: 132-140
Effects of YM155 on survivin levels and viability in neuroblastoma cells with acquired drug resistance

Yvonne Voges
Martin Michaelis
Jindrich Cinatl
ResearchOpen Access13 Oct 2016
Cell Death & Disease

Volume: 7, P: e2410
Culture- and metagenomics-enabled analyses of the Methanosphaera genus reveals their monophyletic origin and differentiation according to genome size

Emily C. Hoedt
Donovan H. Parks
Mark Morrison
Research01 Aug 2018
The ISME Journal

Volume: 12, P: 2942-2953
Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations

Lance H. Rodan
Rebecca C. Spillmann
Vandana Shashi
Research23 Jun 2021
Genetics in Medicine

Volume: 23, P: 1922-1932
Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain

Felix Marbach
Georgi Stoyanov
Christian P. Schaaf
ResearchOpen Access08 Apr 2021
Genetics in Medicine

Volume: 23, P: 1465-1473
Sharing brain mapping statistical results with the neuroimaging data model

Camille Maumet
Tibor Auer
Thomas E. Nichols
ResearchOpen Access06 Dec 2016
Scientific Data

Volume: 3, P: 1-15
Temporal Pattern of Cocaine Intake Determines Tolerance vs Sensitization of Cocaine Effects at the Dopamine Transporter

Erin S Calipari
Mark J Ferris
Sara R Jones
Research30 May 2013
Neuropsychopharmacology

Volume: 38, P: 2385-2392
Prediction of short-term neonatal complications in preterm infants using exome-wide genetic variation and gestational age: a pilot study

William C. L. Stewart
Komla M. Gnona
Leif D. Nelin
Research05 Feb 2020
Pediatric Research

Volume: 88, P: 653-660
Author Correction: Cancer LncRNA Census reveals evidence for deep functional conservation of long noncoding RNAs in tumorigenesis

Joana Carlevaro-Fita
Andrés Lanzós
Christian von Mering
Amendments and CorrectionsOpen Access08 Dec 2022
Communications Biology

Volume: 5, P: 1
Author Correction: The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities

Eric Venner
Karynne Patterson
Miriam Vos
Amendments and CorrectionsOpen Access10 Jun 2024
Communications Biology

Volume: 7, P: 1
Endogenous Opioid Blockade and Impulsive Responding in Alcoholics and Healthy Controls

Jennifer M Mitchell
Venessa C Tavares
Charlotte A Boettiger
Research18 Oct 2006
Neuropsychopharmacology

Volume: 32, P: 439-449
The retrospective analysis of Antarctic tracking data project

Yan Ropert-Coudert
Anton P. Van de Putte
Mark A. Hindell
ResearchOpen Access18 Mar 2020
Scientific Data

Volume: 7, P: 1-11
Physiological and perceived health effects from daily changes in air pollution and weather among persons with heart failure: A panel study

Mark S Goldberg
Amanda J Wheeler
Nadia Giannetti
Research18 Jun 2014
Journal of Exposure Science & Environmental Epidemiology

Volume: 25, P: 187-199
Within- and between-city contrasts in nitrogen dioxide and mortality in 10 Canadian cities; a subset of the Canadian Census Health and Environment Cohort (CanCHEC)

Dan L Crouse
Paul A Peters
Richard T Burnett
ResearchOpen Access21 Jan 2015
Journal of Exposure Science & Environmental Epidemiology

Volume: 25, P: 482-489
Exclusion Mapping of Classical Late Infantile Neuronal Ceroid Lipofuscinosis (Jansky-Bielschowsky Disease, CLN2)

Julie D. Sharp
Ruth B. Wheeler
Ruth Williams
Correspondence01 Sept 1995
European Journal of Human Genetics

Volume: 3, P: 326-328
Correction to: An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids

Sacha Ferdinandusse
Kirsty McWalter
Frédéric M. Vaz
Amendments and CorrectionsOpen Access19 Oct 2021
Genetics in Medicine

Volume: 23, P: 2467
Erratum: Genomes and phenomes of a population of outbred rats and its progenitors

Amelie Baud
Victor Guryev
Jonathan Flint
Amendments and Corrections08 Jul 2014
Scientific Data

Volume: 1, P: 1
Genomes and phenomes of a population of outbred rats and its progenitors

Amelie Baud
Victor Guryev
Jonathan Flint
ResearchOpen Access10 Jun 2014
Scientific Data

Volume: 1, P: 1-15
Correction: Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations

Lance H. Rodan
Rebecca C. Spillmann
Vandana Shashi
Amendments and Corrections14 Sept 2021
Genetics in Medicine

Volume: 23, P: 2016

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