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1
Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study

von Okubadejo, Njideka ; Ojo, Oluwadamilola ; Abiodun, Oladunni ; et al.

In The Lancet Neurology November 2023 22(11):1015-1025
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2
MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study

von Warner, Thomas T ; Jaunmuktane, Zane ; Boeve, Bradley F ; et al.

In The Lancet Neurology May 2024 23(5):487-499
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3
Changes in the global hospitalisation burden of respiratory syncytial virus in young children during the COVID-19 pandemic: a systematic analysis

von Mrčela, Dina ; Milić, Petra ; Veljačić Visković, Daniela ; et al.

In The Lancet Infectious Diseases April 2024 24(4):361-374
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4
The clinicopathological features of thrombosis with thrombocytopenia syndrome following ChAdOx1-S (AZD1222) vaccination and case outcomes in Australia: a population-based study

von Tran, Huyen A. ; Deng, Lucy ; Wood, Nicholas ; et al.

In The Lancet Regional Health - Western Pacific November 2023 40
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5
Risk factors and outcomes for recurrent paediatric in-hospital cardiac arrest: Retrospective multicenter cohort study

von Abulebda, Kamal ; Atkins, Diane ; Balikai, Shilpa ; et al.

In Resuscitation December 2021 169:60-66
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6
Heritability and genetic variance of dementia with Lewy bodies

von Guerreiro, Rita ; Escott-Price, Valentina ; Hernandez, Dena G. ; et al.

In Neurobiology of Disease July 2019 127:492-501
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7
Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study

von Guerreiro, Rita ; Ross, Owen A ; Kun-Rodrigues, Celia ; et al.

In The Lancet Neurology January 2018 17(1):64-74
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8
A saturated map of common genetic variants associated with human height

von L Yengo ; S Vedantam ; E Marouli ; et al.

Schlagworte: No keyword
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9
Dietary practices in propionic acidemia: A European survey

von Daly, A. ; Pinto, A. ; Evans, S. ; et al.

In Molecular Genetics and Metabolism Reports December 2017 13:83-89
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10
Global, regional, and national disease burden estimates of acute lower respiratory infections due to respiratory syncytial virus in young children in 2015: a systematic review and modelling study

von Shi, Ting ; McAllister, David A ; O'Brien, Katherine L ; et al.

In The Lancet 2-8 September 2017 390(10098):946-958
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11
A Saturated Map of Common Genetic Variants Associated with Human Height

von Loïc Yengo ; Sailaja Vedantam ; Jenkai Miao ; et al.

Schlagworte: Genetics; Epidemiology; common single-nucleotide polymorphisms (SNPs); human height; genome; ancestry
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12
Dietary practices in isovaleric acidemia: A European survey

von Pinto, A. ; Daly, A. ; Evans, S. ; et al.

In Molecular Genetics and Metabolism Reports September 2017 12:16-22
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13
Frontotemporal dementia and its subtypes: a genome-wide association study

von Ferrari, Raffaele ; Hernandez, Dena G ; Nalls, Michael A ; et al.

In Lancet Neurology July 2014 13(7):686-699
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14
Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study

von Nalls, Mike A ; McLean, Cory Y ; Rick, Jacqueline ; et al.

In The Lancet Neurology October 2015 14(10):1002-1009
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15
How strict is galactose restriction in adults with galactosaemia? International practice

von Adam, S. ; Akroyd, R. ; Bernabei, S. ; et al.

In Molecular Genetics and Metabolism May 2015 115(1):23-26
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16
Years lived with disability (YLDs) for 1160 sequelae of 289 diseases and injuries 1990–2010: a systematic analysis for the Global Burden of Disease Study 2010

von Vos, Theo ; Flaxman, Abraham D ; Naghavi, Mohsen ; et al.

In The Lancet 15 December 2012-4 January 2013 380(9859):2163-2196
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17
Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: a systematic analysis for the Global Burden of Disease Study 2010

von Lozano, Rafael ; Naghavi, Mohsen ; Foreman, Kyle ; et al.

In The Lancet 15 December 2012-4 January 2013 380(9859):2095-2128
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18
Disability-adjusted life years (DALYs) for 291 diseases and injuries in 21 regions, 1990–2010: a systematic analysis for the Global Burden of Disease Study 2010

von Murray, Christopher J L ; Vos, Theo ; Lozano, Rafael ; et al.

In The Lancet 15 December 2012-4 January 2013 380(9859):2197-2223
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19
Global and regional burden of hospital admissions for severe acute lower respiratory infections in young children in 2010: a systematic analysis

von Nair, Harish ; Simões, Eric AF ; Rudan, Igor ; et al.

In The Lancet 20-26 April 2013 381(9875):1380-1390
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20
A Genome-Wide Association Study of Depressive Symptoms

von Hek, Karin ; Demirkan, Ayse ; Lahti, Jari ; et al.

In Biological Psychiatry 1 April 2013 73(7):667-678
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21
Mendelian adult-onset leukodystrophy genes in Alzheimer's disease: critical influence of CSF1R and NOTCH3.

von C Sassi ; MA Nalls ; PG Ridge ; et al.

Schlagworte: Alzheimer's disease; CSF1R; Mendelian leukodystrophies; NOTCH3
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22
Effect modification by population dietary folate on the association between MTHFR genotype, homocysteine, and stroke risk: a meta-analysis of genetic studies and randomised trials

von Holmes, Michael V ; Newcombe, Paul ; Hubacek, Jaroslav A ; et al.

In The Lancet 2011 378(9791):584-594
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23
The commercial genetic testing landscape for Parkinson's disease

von Brice, Alexis ; Kumeh, Amasi ; West, Andrew B. ; et al.

In Parkinsonism and Related Disorders November 2021 92:107-111
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24
Global, regional, and national disease burden estimates of acute lower respiratory infections due to respiratory syncytial virus in children younger than 5 years in 2019: a systematic analysis

von Li, Y ; Wang, X ; Blau, DM ; et al.

Schlagworte: Journal Article
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25
Feasibility and safety of lumbar puncture in the Parkinson's disease research participants: Parkinson's Progression Marker Initiative (PPMI)

von Marek, Kenneth ; Siderowf, Andrew ; Seibyl, John ; et al.

In Parkinsonism and Related Disorders May 2019 62:201-209
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