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ArticlesPeer ReviewedFull Text
APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases
Author / Creator:Lanoiselée, Hélène-Marie ; Nicolas, Gaël ; Wallon, David ; Rovelet-Lecrux, Anne ; Lacour, Morgane ; Rousseau, Stéphane ; Richard, Anne-Claire ; Pasquier, Florence ; Rollin-Sillaire, Adeline ; Martinaud, Olivier ; Quillard-Muraine, Muriel ; de la Sayette, Vincent ; Boutoleau-Bretonniere, Claire ; Etcharry-Bouyx, Frédérique ; Chauviré, Valérie ; Sarazin, Marie ; le Ber, Isabelle ; Epelbaum, Stéphane ; Jonveaux, Thérèse ; Rouaud, Olivier ; Ceccaldi, Mathieu ; Félician, Olivier ; Godefroy, Olivier ; Formaglio, Maite ; Croisile, Bernard ; Auriacombe, Sophie ; Chamard, Ludivine ; Vincent, Jean-Louis ; Sauvée, Mathilde ; Marelli-Tosi, Cecilia ; Gabelle, Audrey ; Ozsancak, Canan ; Pariente, Jérémie ; Paquet, Claire ; Hannequin, Didier ; Campion, Dominique
Publisher:United States: Public Library of Science
Journal title:PLoS medicine, 2017-03, Vol.14 (3), p.e1002270-e1002270
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Publisher Correction: Penetrance estimation of Alzheimer disease in SORL1 loss-of-function variant carriers using a family-based strategy and stratification by APOE genotypes
Author / Creator:Schramm, Catherine ; Charbonnier, Camille ; Zaréa, Aline ; Lacour, Morgane ; Wallon, David ; Boland, Anne ; Deleuze, Jean-François ; Olaso, Robert ; Alarcon, Flora ; Campion, Dominique ; Nuel, Grégory ; Nicolas, Gaël
Publisher:London: BioMed Central Ltd
Journal title:Genome medicine, 2022-08, Vol.14 (1), p.1-83, Article 83
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Penetrance estimation of SORL1 loss-of-function variants using a family-based strategy adjusted on APOE genotypes suggest a non-monogenic inheritance
Author / Creator:Schramm, Catherine ; Charbonnier, Camille ; Zaréa, Aline ; Lacour, Morgane ; Wallon, David ; Collaborators, Cnrmaj ; Boland, Anne ; Deleuze, Jean-François ; Olaso, Robert ; Alarcon, Flora ; Campion, Dominique ; Nuel, Grégory ; Nicolas, Gaël
Publisher:Cold Spring Harbor: Cold Spring Harbor Laboratory Press
Journal title:bioRxiv, 2021-07
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ReportsFull Text
APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases
Author / Creator:Lanoiselée, Hélène-Marie ; Nicolas, Gaël ; Wallon, David ; Rovelet-Lecrux, Anne ; Lacour, Morgane ; Rousseau, Stéphane ; Richard, Anne-Claire ; Pasquier, Florence ; Rollin-Sillaire, Adeline ; Martinaud, Olivier ; Quillard-Muraine, Muriel ; de la Sayette, Vincent ; Boutoleau-Bretonniere, Claire ; Etcharry-Bouyx, Frédérique ; Chauviré, Valérie ; Sarazin, Marie ; le Ber, Isabelle ; Epelbaum, Stéphane ; Jonveaux, Thérèse ; Rouaud, Olivier ; Ceccaldi, Mathieu ; Félician, Olivier ; Godefroy, Olivier ; Formaglio, Maite ; Croisile, Bernard ; Auriacombe, Sophie ; Chamard, Ludivine ; Vincent, Jean-Louis ; Sauvée, Mathilde ; Marelli-Tosi, Cecilia ; Gabelle, Audrey ; Ozsancak, Canan ; Pariente, Jérémie ; Paquet, Claire ; Hannequin, Didier ; Campion, Dominique
Publisher:Public Library of Science
Journal title:PLoS Medicine, 2017, Vol.14 (3)
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ReportsFull Text
APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases
Author / Creator:Lanoiselée, Hélène-Marie ; Nicolas, Gaël ; Wallon, David ; Rovelet-Lecrux, Anne ; Lacour, Morgane ; Rousseau, Stéphane ; Richard, Anne-Claire ; Pasquier, Florence ; Rollin-Sillaire, Adeline ; Martinaud, Olivier ; Quillard-Muraine, Muriel ; de la Sayette, Vincent ; Boutoleau-Bretonniere, Claire ; Etcharry-Bouyx, Frédérique ; Chauviré, Valérie ; Sarazin, Marie ; le Ber, Isabelle ; Epelbaum, Stéphane ; Jonveaux, Thérèse ; Rouaud, Olivier ; Ceccaldi, Mathieu ; Félician, Olivier ; Godefroy, Olivier ; Formaglio, Maite ; Croisile, Bernard ; Auriacombe, Sophie ; Chamard, Ludivine ; Vincent, Jean-Louis ; Sauvée, Mathilde ; Marelli-Tosi, Cecilia ; Gabelle, Audrey ; Ozsancak, Canan ; Pariente, Jérémie ; Paquet, Claire ; Hannequin, Didier ; Campion, Dominique
Publisher:Public Library of Science
Journal title:PLoS Medicine, 2017, Vol.14 (3)
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ArticlesPeer ReviewedFull Text
Penetrance estimation of Alzheimer disease in SORL1 loss-of-function variant carriers using a family-based strategy and stratification by APOE genotypes
Author / Creator:Schramm, Catherine ; Charbonnier, Camille ; Zaréa, Aline ; Lacour, Morgane ; Wallon, David ; Boland, Anne ; Deleuze, Jean-François ; Olaso, Robert ; Alarcon, Flora ; Campion, Dominique ; Nuel, Grégory ; Nicolas, Gaël
Publisher:England: BioMed Central Ltd
Journal title:Genome medicine, 2022-06, Vol.14 (1), p.69-69, Article 69
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APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases

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Publisher Correction: Penetrance estimation of Alzheimer disease in SORL1 loss-of-function variant carriers using a family-based strategy and stratification by APOE genotypes

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Penetrance estimation of SORL1 loss-of-function variants using a family-based strategy adjusted on APOE genotypes suggest a non-monogenic inheritance

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APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases

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APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases

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Penetrance estimation of Alzheimer disease in SORL1 loss-of-function variant carriers using a family-based strategy and stratification by APOE genotypes

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