Ghent University Academic Bibliography

Your filters: cql: author="Van Mossevelde, Sara" or (type any "bookEditor issueEditor" and editor="Van Mossevelde, S...

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- Journal Article
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No association of CpG SNP rs9357140 with onset age in Belgian C9orf72 repeat expansion carriers

Cemile Koçoğlu, Helena Gossye, Lubina Dillen, Sara Van Mossevelde, Jan De Bleecker (UGent) , Rik Vandenberghe, Peter P. De Deyn, Kristel Sleegers, Patrick Cras, Sebastiaan Engelborghs, et al.

(2021) NEUROBIOLOGY OF AGING. 97. p.145.e1-145.e4
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- Miscellaneous
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Homozygous and compound heterozygous rare variants in VPS13C contribute to Lewy body diseases

Stefanie Smolders, Stéphanie Philtjens, David Crosiers, Anne Sieben, Elisabeth Hens, Bavo Heeman, Sara Van Mossevelde, Philippe Pals, Bob Asselbergh, Roberto Dos Santos Dias, et al.

(2020) Research Square.
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Loss of DPP6 in neurodegenerative dementia : a genetic player in the dysfunction of neuronal excitability

Rita Cacace, Bavo Heeman, Sara Van Mossevelde, Arne De Roeck, Julie Hoogmartens, Peter De Rijk, Helena Gossye, Kristof De Vos, Wouter De Coster, Mojca Strazisar, et al.

(2019) ACTA NEUROPATHOLOGICA. 137(6). p.901-918
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Teenage-onset progressive myoclonic epilepsy due to a familial C9orf72 repeat expansion

Jelle van den Ameele (UGent) , Ivana Jedlickova, Anna Pristoupilova, Anne Sieben, Sara Van Mossevelde, Chantal Ceuterick-de Groote, Helena Hůlková, Radoslav Matej, Alfred Meurs, Christine Van Broeckhoven, et al.

(2018) NEUROLOGY. 90(8). p.e658-e663
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Extended FTLD pedigree segregating a Belgian GRN-null mutation : neuropathological heterogeneity in one family

Anne Sieben, Sara Van Mossevelde, Eline Wauters, Sebastiaan Engelborghs, Julie van der Zee, Tim Van Langenhove (UGent) , Patrick Santens (UGent) , Marleen Praet, Paul Boon (UGent) , Marijke Miatton (UGent) , et al.

(2018) ALZHEIMERS RESEARCH & THERAPY. 10.
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Clinical variability and onset age modifiers in an extended Belgian GRN founder family

Eline Wauters, Sara Van Mossevelde, Kristel Sleegers, Julie van der Zee, Sebastiaan Engelborghs, Anne Sieben, Rik Vandenberghe, Stephanie Philtjens, Marleen Van den Broeck, Karin Peeters, et al.

(2018) NEUROBIOLOGY OF AGING. 67. p.84-94
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No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients

Yalda Baradaran-Heravi, Lubina Dillen, Hung Phuoc Nguyen, Sara Van Mossevelde, Jonathan Baets, Peter De Jonghe, Sebastiaan Engelborghs, Peter P De Deyn, Mathieu Vandenbulcke, Rik Vandenberghe, et al.

(2018) NEUROBIOLOGY OF AGING. 69.
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Investigating the role of ALS genes CHCHD10 and TUBA4A in Belgian FTD-ALS spectrum patients

Federica Perrone, Hung Phuoc Nguyen, Sara Van Mossevelde, Matthieu Moisse, Anne Sieben, Patrick Santens (UGent) , Jan De Bleecker (UGent) , Mathieu Vandenbulcke, Sebastiaan Engelborghs, Jonathan Baets, et al.

(2017) NEUROBIOLOGY OF AGING. 51. p.177.e9-177.e16
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Clinical evidence of disease anticipation in families segregating a C9orf72 repeat expansion

Sara Van Mossevelde, Julie van der Zee, Ilse Gijselinck, Kristel Sleegers, Jan De Bleecker (UGent) , Anne Sieben, Rik Vandenberghe, Tim Van Langenhove (UGent) , Jonathan Baets, Olivier Deryck, et al.

(2017) JAMA NEUROLOGY. 74(4). p.445-452
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TBK1 mutation spectrum in an extended European patient cohort with frontotemporal dementia and amyotrophic lateral sclerosis

Julie van der Zee, Ilse Gijselinck, Sara Van Mossevelde, Federica Perrone, Lubina Dillen, Bavo Heeman, Veerle Bäumer, Sebastiaan Engelborghs, Jan De Bleecker (UGent) , Jonathan Baets, et al.

(2017) HUMAN MUTATION. 38(3). p.297-309

Academic Bibliography

No association of CpG SNP rs9357140 with onset age in Belgian C9orf72 repeat expansion carriers

Homozygous and compound heterozygous rare variants in VPS13C contribute to Lewy body diseases

Loss of DPP6 in neurodegenerative dementia : a genetic player in the dysfunction of neuronal excitability

Teenage-onset progressive myoclonic epilepsy due to a familial C9orf72 repeat expansion

Extended FTLD pedigree segregating a Belgian GRN-null mutation : neuropathological heterogeneity in one family

Clinical variability and onset age modifiers in an extended Belgian GRN founder family

No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients

Investigating the role of ALS genes CHCHD10 and TUBA4A in Belgian FTD-ALS spectrum patients

Clinical evidence of disease anticipation in families segregating a C9orf72 repeat expansion

TBK1 mutation spectrum in an extended European patient cohort with frontotemporal dementia and amyotrophic lateral sclerosis

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