Pihlstrom, Lasse: search on Z-Library

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1

Deep brain stimulation and genetic variability in Parkinson’s disease: a review of the literature

Ligaard, Johanne, Sannæs, Julia, Pihlstrøm, Lasse

Journal:

npj Parkinson s Disease

Year:

2019

File:

PDF, 722 KB

2019

2

NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases

Blauwendraat, Cornelis, Faghri, Faraz, Pihlstrom, Lasse, Geiger, Joshua T., Elbaz, Alexis, Lesage, Suzanne, Corvol, Jean-Christophe, May, Patrick, Nicolas, Aude, Abramzon, Yevgeniya, Murphy, Natalie A

Journal:

Neurobiology of Aging

Year:

2017

Language:

english

File:

PDF, 726 KB

english, 2017

3

Deep brain stimulation and genetic variability in Parkinson’s disease: a review of the literature

Ligaard, Johanne, Sannæs, Julia, Pihlstrøm, Lasse

Journal:

npj Parkinson s Disease

Year:

2019

Language:

english

File:

PDF, 722 KB

english, 2019

4

Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease

Blauwendraat, Cornelis, Reed, Xylena, Kia, Demis A., Gan-Or, Ziv, Lesage, Suzanne, Pihlstrøm, Lasse, Guerreiro, Rita, Gibbs, J. Raphael, Sabir, Marya, Ahmed, Sarah, Ding, Jinhui, Alcalay, Roy N., Hass

Journal:

Year:

2018

Language:

english

File:

PDF, 277 KB

english, 2018

5

Understanding the role of genetic variability in LRRK2 in Indian population

Kishore, Asha, Ashok Kumar Sreelatha, Ashwin, Sturm, Marc, von-Zweydorf, Felix, Pihlstrøm, Lasse, Raimondi, Francesco, Russell, Rob, Lichtner, Peter, Banerjee, Moinak, Krishnan, Syam, Rajan, Roopa, Pu

Journal:

Movement Disorders

Year:

2018

Language:

english

File:

PDF, 362 KB

english, 2018

6

Genetic variability inSNCAand Parkinson’s disease

Lasse Pihlstrøm, Mathias Toft

Journal:

Year:

2011

Language:

english

File:

PDF, 486 KB

english, 2011

7

A cumulative genetic risk score predicts progression in Parkinson's disease

Pihlstrøm, Lasse, Morset, Kristina Rebekka, Grimstad, Espen, Vitelli, Valeria, Toft, Mathias

Journal:

Movement Disorders

Year:

2016

Language:

english

File:

PDF, 331 KB

english, 2016

8

LRP10 in α-synucleinopathies

Pihlstrøm, Lasse, Schottlaender, Lucia, Chelban, Viorica, Houlden, Henry, Al-Sarraj, Safa, Arzberger, Thomas, Bettencourt, Conceicao, Bhatia, Kailash, Dickson, Dennis W, Federoff, Monica, Gelpi, Ellen

Journal:

The Lancet Neurology

Year:

2018

Language:

english

File:

PDF, 56 KB

english, 2018

9

ARSA variants in α-synucleinopathies

Makarious, Mary B, Diez-Fairen, Monica, Krohn, Lynne, Blauwendraat, Cornelis, Bandres-Ciga, Sara, Ding, Jinhui, Pihlstrøm, Lasse, Houlden, Henry, Scholz, Sonja W, Gan-Or, Ziv

Journal:

Year:

2019

Language:

english

File:

PDF, 425 KB

english, 2019

10

The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease

Lill, Christina M., Rengmark, Aina, Pihlstrøm, Lasse, Fogh, Isabella, Shatunov, Aleksey, Sleiman, Patrick M., Wang, Li-San, Liu, Tian, Lassen, Christina F., Meissner, Esther, Alexopoulos, Panos, Calvo

Journal:

Alzheimer's & Dementia

Year:

2015

Language:

english

File:

PDF, 1.04 MB

english, 2015

11

Fine mapping and resequencing of the PARK16 locus in Parkinson’s disease

Pihlstrøm, Lasse, Rengmark, Aina, Bjørnarå, Kari Anne, Dizdar, Nil, Fardell, Camilla, Forsgren, Lars, Holmberg, Björn, Larsen, Jan Petter, Linder, Jan, Nissbrandt, Hans, Tysnes, Ole-Bjørn, Dietrichs,

Journal:

Journal of Human Genetics

Year:

2015

Language:

english

File:

PDF, 500 KB

english, 2015

12

Cumulative genetic risk and age at onset in Parkinson's disease

Pihlstrøm, Lasse, Toft, Mathias

Journal:

Movement Disorders

Year:

2015

Language:

english

File:

PDF, 122 KB

english, 2015

13

Parkinson's disease: What remains of the “missing heritability”?

Lasse Pihlstrøm, Mathias Toft

Journal:

Movement Disorders

Year:

2011

Language:

english

File:

PDF, 71 KB

english, 2011

14

[Handbook of Clinical Neurology] Neuropathology Volume 145 || Genetics of neurodegenerative diseases: an overview

Pihlstrøm, Lasse

Year:

2017

Language:

english

File:

PDF, 484 KB

english, 2017

15

A comprehensive analysis of SNCA -related genetic risk in sporadic parkinson disease

Pihlstrøm, Lasse, Blauwendraat, Cornelis, Cappelletti, Chiara, Berge-Seidl, Victoria, Langmyhr, Margrete, Henriksen, Sandra Pilar, van de Berg, Wilma D. J., Gibbs, J. Raphael, Cookson, Mark R., Single

Journal:

Annals of Neurology

Year:

2018

Language:

english

File:

PDF, 581 KB

english, 2018

16

Effective Variant Detection by Targeted Deep Sequencing of DNA Pools: An Example from Parkinson's Disease

Pihlstrøm, Lasse, Rengmark, Aina, Bjørnarå, Kari Anne, Toft, Mathias

Journal:

Annals of Human Genetics

Year:

2014

Language:

english

File:

PDF, 428 KB

english, 2014

17

The endocytic membrane trafficking pathway plays a major role in the risk of Parkinson's disease

Bandres-Ciga, Sara, Saez-Atienzar, Sara, Bonet-Ponce, Luis, Billingsley, Kimberley, Vitale, Dan, Blauwendraat, Cornelis, Gibbs, Jesse Raphael, Pihlstrøm, Lasse, Gan-Or, Ziv, Cookson, Mark R., Nalls, M

Journal:

Movement Disorders

Year:

2019

File:

PDF, 517 KB

2019

18

Insufficient evidence for pathogenicity of SNCA His50Gln (H50Q) in Parkinson’s disease

Blauwendraat, Cornelis, Kia, Demis A., Pihlstrom, Lasse, Gan-Or, Ziv, Lesage, Suzanne, Gibbs, J. Raphael, Ding, Jinhui, Alcalay, Roy N., Hassin-Baer, Sharon, Pittman, Alan M., Brooks, Janet, Edsall, C

Journal:

Neurobiology of Aging

Year:

2017

Language:

english

File:

PDF, 364 KB

english, 2017

19

Genetic modifier of LRRK2-parkinsonism is not transferable to idiopathic disease No evidence for DNM3 as genetic modifier of age at onset in idiopathic Parkinson's disease

Berge-Seidl, Victoria, Pihlstrøm, Lasse, Wszolek, Zbigniew K., Ross, Owen A., Toft, Mathias

Journal:

Neurobiology of Aging

Year:

2018

Language:

english

File:

PDF, 317 KB

english, 2018

20

A paradoxical relationship between family history, onset age, and genetic risk in Parkinson's disease

Kristiansen, Madeleine, Maple-Grødem, Jodi, Alves, Guido, Arepalli, Sampath, Hernandez, Dena G., Iwaki, Hirotaka, Nalls, Mike A., Singleton, Andrew, Tysnes, Ole-Bjørn, Toft, Mathias, Pihlstrøm, Lasse

Journal:

Movement Disorders

Year:

2018

Language:

english

File:

PDF, 121 KB

english, 2018

21

The GBA variant E326K is associated with Parkinson's disease and explains a genome-wide association signal

Berge-Seidl, Victoria, Pihlstrøm, Lasse, Maple-Grødem, Jodi, Forsgren, Lars, Linder, Jan, Larsen, Jan Petter, Tysnes, Ole-Bjørn, Toft, Mathias

Journal:

Neuroscience Letters

Year:

2017

Language:

english

File:

PDF, 228 KB

english, 2017

22

Missense mutations in DYT-TOR1A dystonia

Iqbal, Zafar, Koht, Jeanette, Pihlstrøm, Lasse, Henriksen, Sandra P., Cappelletti, Chiara, Russel, Michael Bjørn, Norberto de Souza, Osmar, Skogseid, Inger Marie, Toft, Mathias

Journal:

Neurology: Genetics

Year:

2019

Language:

english

File:

PDF, 330 KB

english, 2019

23

Parkinson's disease correlates with promoter methylation in the α-synuclein gene

Pihlstrøm, Lasse, Berge, Victoria, Rengmark, Aina, Toft, Mathias

Journal:

Movement Disorders

Year:

2015

Language:

english

File:

PDF, 254 KB

english, 2015

24

Lysosomal storage disorder gene variants in multiple system atrophy

Pihlstrøm, Lasse, Schottlaender, Lucia, Chelban, Viorica, Meissner, Wassilios G, Federoff, Monica, Singleton, Andy, Houlden, Henry

Journal:

Year:

2018

Language:

english

File:

PDF, 232 KB

english, 2018

25

Genomewide association study of Parkinson's disease clinical biomarkers in 12 longitudinal patients' cohorts

Iwaki, Hirotaka, Blauwendraat, Cornelis, Leonard, Hampton L., Kim, Jonggeol J., Liu, Ganqiang, Maple‐Grødem, Jodi, Corvol, Jean‐Christophe, Pihlstrøm, Lasse, Nimwegen, Marlies, Hutten, Samantha J., Ng

Journal:

Movement Disorders

Year:

2019

File:

PDF, 1.38 MB

2019

26

Genomewide association study of Parkinson's disease clinical biomarkers in 12 longitudinal patients' cohorts

Iwaki, Hirotaka, Blauwendraat, Cornelis, Leonard, Hampton L., Kim, Jonggeol J., Liu, Ganqiang, Maple‐Grødem, Jodi, Corvol, Jean‐Christophe, Pihlstrøm, Lasse, Nimwegen, Marlies, Hutten, Samantha J., Ng

Journal:

Movement Disorders

Year:

2019

Language:

english

File:

PDF, 1.38 MB

english, 2019

27

Supportive evidence for 11 loci from genome-wide association studies in Parkinson's disease

Pihlstrøm, Lasse, Axelsson, Gunnar, Bjørnarå, Kari Anne, Dizdar, Nil, Fardell, Camilla, Forsgren, Lars, Holmberg, Björn, Larsen, Jan Petter, Linder, Jan, Nissbrandt, Hans, Tysnes, Ole-Bjørn, Öhman, Ei

Journal:

Neurobiology of Aging

Year:

2013

Language:

english

File:

PDF, 250 KB

english, 2013

28

Genetic risk of Parkinson disease and progression:

Iwaki, Hirotaka, Blauwendraat, Cornelis, Leonard, Hampton L., Liu, Ganqiang, Maple-Grødem, Jodi, Corvol, Jean-Christophe, Pihlstrøm, Lasse, van Nimwegen, Marlies, Hutten, Samantha J., Nguyen, Khanh-Du

Journal:

Neurology: Genetics

Year:

2019

Language:

english

File:

PDF, 1.03 MB

english, 2019

29

Analysis of the prion protein gene in multiple system atrophy

Chelban, Viorica, Manole, Andreea, Pihlstrøm, Lasse, Schottlaender, Lucia, Efthymiou, Stephanie, OConnor, Emer, Meissner, Wassilios, Holton, Janice L., Houlden, Henry

Journal:

Neurobiology of Aging

Year:

2016

Language:

english

File:

PDF, 698 KB

english, 2016

30

Correction: Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia

Iqbal, Zafar, Rydning, Siri L., Wedding, Iselin M., Koht, Jeanette, Pihlstrøm, Lasse, Rengmark, Aina H., Henriksen, Sandra P., Tallaksen, Chantal M. E., Toft, Mathias

Journal:

Year:

2017

Language:

english

File:

PDF, 299 KB

english, 2017

31

Low frequency of GCH1 and TH mutations in Parkinson's disease

Rengmark, Aina, Pihlstrøm, Lasse, Linder, Jan, Forsgren, Lars, Toft, Mathias

Journal:

Parkinsonism & Related Disorders

Year:

2016

Language:

english

File:

PDF, 192 KB

english, 2016

32

Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia

Iqbal, Zafar, Rydning, Siri L., Wedding, Iselin M., Koht, Jeanette, Pihlstrøm, Lasse, Rengmark, Aina H., Henriksen, Sandra P., Tallaksen, Chantal M. E., Toft, Mathias, Brusgaard, Klaus

Journal:

Year:

2017

Language:

english

File:

PDF, 1.98 MB

english, 2017

33

Rare variants in dementia genes and Parkinson’s disease

Iqbal, Zafar, Pihlstrøm, Lasse, Rengmark, Aina, Henriksen, Sandra Pilar, Linder, Jan, Forsgren, Lars, Toft, Mathias

Journal:

European Journal of Human Genetics

Year:

2016

Language:

english

File:

PDF, 114 KB

english, 2016

34

Risk variants of the α-synuclein locus and REM sleep behavior disorder in Parkinson’s disease: a genetic association study

Bjørnarå, Kari Anne, Pihlstrøm, Lasse, Dietrichs, Espen, Toft, Mathias

Journal:

Year:

2018

Language:

english

File:

PDF, 391 KB

english, 2018

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