LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study

M. Quadri, W. Mandemakers, M.M. Grochowska, R. Masius, H. Geut, E. Fabrizio, G.J. Breedveld, D. Kuipers, M. Minneboo, L.J.M. Vergouw, A. Carreras Mascaro, E. Yonova-Doing, E. Simons, T. Zhao, A.B. Di Fonzo, H.-C. Chang, P. Parchi, M. Melis, L. Correia Guedes, C. CriscuoloA. Thomas, R.W.W. Brouwer, D. Heijsman, A.M.T. Ingrassia, G. Calandra Buonaura, J.P. Rood, S. Capellari, A.J. Rozemuller, M. Sarchioto, H. Fen Chien, N. Vanacore, S. Olgiati, Y.-H. Wu-Chou, T.-H. Yeh, A.J.W. Boon, S.E. Hoogers, M. Ghazvini, A.S. IJpma, W.F.J. van IJcken, M. Onofrj, P. Barone, D.J. Nicholl, A. Puschmann, M. De Mari, A.J. Kievit, E. Barbosa, G. De Michele, D. Majoor-Krakauer, J.C. van Swieten, F.J. de Jong, J.J. Ferreira, G. Cossu, C.-S. Lu, G. Meco, P. Cortelli, W.D.J. van de Berg, V. Bonifati, International Parkinsonism Genetics Network

Research output: Contribution to journalArticle

Original languageEnglish
Pages (from-to)597-608
Number of pages12
JournalThe Lancet Neurology
Volume17
Issue number7
DOIs
Publication statusPublished - 2018

Cite this

Quadri, M., Mandemakers, W., Grochowska, M. M., Masius, R., Geut, H., Fabrizio, E., ... Network, I. P. G. (2018). LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study. The Lancet Neurology, 17(7), 597-608. https://doi.org/10.1016/S1474-4422(18)30179-0

LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study. / Quadri, M.; Mandemakers, W.; Grochowska, M.M.; Masius, R.; Geut, H.; Fabrizio, E.; Breedveld, G.J.; Kuipers, D.; Minneboo, M.; Vergouw, L.J.M.; Carreras Mascaro, A.; Yonova-Doing, E.; Simons, E.; Zhao, T.; Di Fonzo, A.B.; Chang, H.-C.; Parchi, P.; Melis, M.; Correia Guedes, L.; Criscuolo, C.; Thomas, A.; Brouwer, R.W.W.; Heijsman, D.; Ingrassia, A.M.T.; Calandra Buonaura, G.; Rood, J.P.; Capellari, S.; Rozemuller, A.J.; Sarchioto, M.; Fen Chien, H.; Vanacore, N.; Olgiati, S.; Wu-Chou, Y.-H.; Yeh, T.-H.; Boon, A.J.W.; Hoogers, S.E.; Ghazvini, M.; IJpma, A.S.; van IJcken, W.F.J.; Onofrj, M.; Barone, P.; Nicholl, D.J.; Puschmann, A.; De Mari, M.; Kievit, A.J.; Barbosa, E.; De Michele, G.; Majoor-Krakauer, D.; van Swieten, J.C.; de Jong, F.J.; Ferreira, J.J.; Cossu, G.; Lu, C.-S.; Meco, G.; Cortelli, P.; van de Berg, W.D.J.; Bonifati, V.; Network, International Parkinsonism Genetics.

In: The Lancet Neurology, Vol. 17, No. 7, 2018, p. 597-608.

Research output: Contribution to journalArticle

Quadri, M, Mandemakers, W, Grochowska, MM, Masius, R, Geut, H, Fabrizio, E, Breedveld, GJ, Kuipers, D, Minneboo, M, Vergouw, LJM, Carreras Mascaro, A, Yonova-Doing, E, Simons, E, Zhao, T, Di Fonzo, AB, Chang, H-C, Parchi, P, Melis, M, Correia Guedes, L, Criscuolo, C, Thomas, A, Brouwer, RWW, Heijsman, D, Ingrassia, AMT, Calandra Buonaura, G, Rood, JP, Capellari, S, Rozemuller, AJ, Sarchioto, M, Fen Chien, H, Vanacore, N, Olgiati, S, Wu-Chou, Y-H, Yeh, T-H, Boon, AJW, Hoogers, SE, Ghazvini, M, IJpma, AS, van IJcken, WFJ, Onofrj, M, Barone, P, Nicholl, DJ, Puschmann, A, De Mari, M, Kievit, AJ, Barbosa, E, De Michele, G, Majoor-Krakauer, D, van Swieten, JC, de Jong, FJ, Ferreira, JJ, Cossu, G, Lu, C-S, Meco, G, Cortelli, P, van de Berg, WDJ, Bonifati, V & Network, IPG 2018, 'LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study', The Lancet Neurology, vol. 17, no. 7, pp. 597-608. https://doi.org/10.1016/S1474-4422(18)30179-0
Quadri, M. ; Mandemakers, W. ; Grochowska, M.M. ; Masius, R. ; Geut, H. ; Fabrizio, E. ; Breedveld, G.J. ; Kuipers, D. ; Minneboo, M. ; Vergouw, L.J.M. ; Carreras Mascaro, A. ; Yonova-Doing, E. ; Simons, E. ; Zhao, T. ; Di Fonzo, A.B. ; Chang, H.-C. ; Parchi, P. ; Melis, M. ; Correia Guedes, L. ; Criscuolo, C. ; Thomas, A. ; Brouwer, R.W.W. ; Heijsman, D. ; Ingrassia, A.M.T. ; Calandra Buonaura, G. ; Rood, J.P. ; Capellari, S. ; Rozemuller, A.J. ; Sarchioto, M. ; Fen Chien, H. ; Vanacore, N. ; Olgiati, S. ; Wu-Chou, Y.-H. ; Yeh, T.-H. ; Boon, A.J.W. ; Hoogers, S.E. ; Ghazvini, M. ; IJpma, A.S. ; van IJcken, W.F.J. ; Onofrj, M. ; Barone, P. ; Nicholl, D.J. ; Puschmann, A. ; De Mari, M. ; Kievit, A.J. ; Barbosa, E. ; De Michele, G. ; Majoor-Krakauer, D. ; van Swieten, J.C. ; de Jong, F.J. ; Ferreira, J.J. ; Cossu, G. ; Lu, C.-S. ; Meco, G. ; Cortelli, P. ; van de Berg, W.D.J. ; Bonifati, V. ; Network, International Parkinsonism Genetics. / LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study. In: The Lancet Neurology. 2018 ; Vol. 17, No. 7. pp. 597-608.
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title = "LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study",
author = "M. Quadri and W. Mandemakers and M.M. Grochowska and R. Masius and H. Geut and E. Fabrizio and G.J. Breedveld and D. Kuipers and M. Minneboo and L.J.M. Vergouw and {Carreras Mascaro}, A. and E. Yonova-Doing and E. Simons and T. Zhao and {Di Fonzo}, A.B. and H.-C. Chang and P. Parchi and M. Melis and {Correia Guedes}, L. and C. Criscuolo and A. Thomas and R.W.W. Brouwer and D. Heijsman and A.M.T. Ingrassia and {Calandra Buonaura}, G. and J.P. Rood and S. Capellari and A.J. Rozemuller and M. Sarchioto and {Fen Chien}, H. and N. Vanacore and S. Olgiati and Y.-H. Wu-Chou and T.-H. Yeh and A.J.W. Boon and S.E. Hoogers and M. Ghazvini and A.S. IJpma and {van IJcken}, W.F.J. and M. Onofrj and P. Barone and D.J. Nicholl and A. Puschmann and {De Mari}, M. and A.J. Kievit and E. Barbosa and {De Michele}, G. and D. Majoor-Krakauer and {van Swieten}, J.C. and {de Jong}, F.J. and J.J. Ferreira and G. Cossu and C.-S. Lu and G. Meco and P. Cortelli and {van de Berg}, W.D.J. and V. Bonifati and Network, {International Parkinsonism Genetics}",
note = "Ricercatori distaccati presso IRCCS a seguito Convenzione esclusiva con Universit{\`a} di Bologna (Parchi Piero,Calandra-Buonaura Giovanna, Capellari Sabina, Cortelli Pietro). Richiesto CORRIGENDUM per modifica di affiliazione (affiliazione imprecisa).",
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TY - JOUR

T1 - LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study

AU - Quadri, M.

AU - Mandemakers, W.

AU - Grochowska, M.M.

AU - Masius, R.

AU - Geut, H.

AU - Fabrizio, E.

AU - Breedveld, G.J.

AU - Kuipers, D.

AU - Minneboo, M.

AU - Vergouw, L.J.M.

AU - Carreras Mascaro, A.

AU - Yonova-Doing, E.

AU - Simons, E.

AU - Zhao, T.

AU - Di Fonzo, A.B.

AU - Chang, H.-C.

AU - Parchi, P.

AU - Melis, M.

AU - Correia Guedes, L.

AU - Criscuolo, C.

AU - Thomas, A.

AU - Brouwer, R.W.W.

AU - Heijsman, D.

AU - Ingrassia, A.M.T.

AU - Calandra Buonaura, G.

AU - Rood, J.P.

AU - Capellari, S.

AU - Rozemuller, A.J.

AU - Sarchioto, M.

AU - Fen Chien, H.

AU - Vanacore, N.

AU - Olgiati, S.

AU - Wu-Chou, Y.-H.

AU - Yeh, T.-H.

AU - Boon, A.J.W.

AU - Hoogers, S.E.

AU - Ghazvini, M.

AU - IJpma, A.S.

AU - van IJcken, W.F.J.

AU - Onofrj, M.

AU - Barone, P.

AU - Nicholl, D.J.

AU - Puschmann, A.

AU - De Mari, M.

AU - Kievit, A.J.

AU - Barbosa, E.

AU - De Michele, G.

AU - Majoor-Krakauer, D.

AU - van Swieten, J.C.

AU - de Jong, F.J.

AU - Ferreira, J.J.

AU - Cossu, G.

AU - Lu, C.-S.

AU - Meco, G.

AU - Cortelli, P.

AU - van de Berg, W.D.J.

AU - Bonifati, V.

AU - Network, International Parkinsonism Genetics

N1 - Ricercatori distaccati presso IRCCS a seguito Convenzione esclusiva con Università di Bologna (Parchi Piero,Calandra-Buonaura Giovanna, Capellari Sabina, Cortelli Pietro). Richiesto CORRIGENDUM per modifica di affiliazione (affiliazione imprecisa).

PY - 2018

Y1 - 2018

U2 - 10.1016/S1474-4422(18)30179-0

DO - 10.1016/S1474-4422(18)30179-0

M3 - Article

C2 - 29887161

VL - 17

SP - 597

EP - 608

JO - The Lancet Neurology

JF - The Lancet Neurology

SN - 1474-4422

IS - 7

ER -