17q21.31 duplication causes prominent tau-related dementia with increased MAPT expression

Authors: Le Guennec, K., Quenez, O., Nicolas, G., Wallon, D., Rousseau, S., Richard, A. C., Alexander, J., Paschou, P., Charbonnier, C., Bellenguez, C.

Source: MOLECULAR PSYCHIATRY. 22(8):1119-1125

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN385685590&indx=1&recIds=ETOCRN385685590

SORL1 rare variants: a major risk factor for familial early-onset Alzheimer’s disease

Authors: Nicolas, G., Charbonnier, C., Wallon, D., Quenez, O., Bellenguez, C., Grenier-Boley, B., Rousseau, S., Richard, A. C., Rovelet-Lecrux, A., Le Guennec, K.

Source: MOLECULAR PSYCHIATRY. 21(6):831-836

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN377532466&indx=1&recIds=ETOCRN377532466

Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons

Authors: Nicolas, G., Wallon, D., Charbonnier, C., Quenez, O., Rousseau, S., Richard, A. C., Rovelet-Lecrux, A., Coutant, S., Le Guennec, K., Bacq, D.

Source: EUROPEAN JOURNAL OF HUMAN GENETICS. 24(5):710-716

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ABCA7 rare variants and Alzheimer disease risk

Authors: Le Guennec, K., Nicolas, G., Quenez, O., Charbonnier, C., Wallon, D., Bellenguez, C., Grenier-Boley, B., Rousseau, S., Richard, A.-C., Rovelet-Lecrux, A.

Source: Neurology. 86(23):2134-2137

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN606742070&indx=1&recIds=ETOCRN606742070

Alzheimer disease: modeling an Aβ-centered biological network

Authors: Campion, D., Pottier, C., Nicolas, G., Le Guennec, K., Rovelet-Lecrux, A.

Source: MOLECULAR PSYCHIATRY. 21(7):861-871

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN378856072&indx=1&recIds=ETOCRN378856072

De novo deleterious genetic variations target a biological network centered on Aβ peptide in early-onset Alzheimer disease

Authors: Rovelet-Lecrux, A, Charbonnier, C, Wallon, D, Nicolas, G, Seaman, M N J, Pottier, C, Breusegem, S Y, Mathur, P P, Jenardhanan, P, Le Guennec, K, Mukadam, A S, Quenez, O, Coutant, S, Rousseau, S, Richard, A-C, Boland, A, Deleuze, J-F, Frebourg, T, Hannequin, D, Campion, D

Source: Molecular psychiatry. 20(9):1046-1056

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100194144043.0x000001&indx=1&recIds=ETOCvdc_100194144043.0x000001

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SORL1rare variants: a major risk factor for familial early-onset Alzheimer’s disease

Authors: Nicolas, G, Charbonnier, C, Wallon, D, Quenez, O, Bellenguez, C, Grenier-Boley, B, Rousseau, S, Richard, A-C, Rovelet-Lecrux, A, Le Guennec, K, Bacq, D, Garnier, J-G, Olaso, R, Boland, A, Meyer, V, Deleuze, J-F, Amouyel, P, Munter, H M, Bourque, G, Lathrop, M, Frebourg, T, Redon, R, Letenneur, L, Dartigues, J-F, Génin, E, Lambert, J-C, Hannequin, D, Campion, D

Source: Molecular Psychiatry; June 2016, Vol. 21 Issue: 6 p831-836, 6p

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