Familial predisposition to TP53/complex karyotype MDS and leukemia in DNA repair-deficient xeroderma pigmentosum

Alain Sarasin; Samuel Quentin; Nathalie Droin; Mourad Sahbatou; Véronique Saada; Nathalie Auger; Yannick Boursin; Philippe Dessen; Anna Raimbault; Vahid Asnafi; Jean Luc Schmutz; Alain Taïeb; Carlos F.M. Menck; Filippo Rosselli; Laurianne Drieu La Rochelle; Caroline Robert; Flore Sicre De Fontbrune; Marie Sébert; Thierry Leblanc; Patricia Kannouche; Stéphane De Botton; Eric Solary; Jean Soulier

doi:10.1182/blood-2019-01-895698

Familial predisposition to TP53/complex karyotype MDS and leukemia in DNA repair-deficient xeroderma pigmentosum

Alain Sarasin, Samuel Quentin, Nathalie Droin, Mourad Sahbatou, Véronique Saada, Nathalie Auger, Yannick Boursin, Philippe Dessen, Anna Raimbault, Vahid Asnafi, Jean Luc Schmutz, Alain Taïeb, Carlos F.M. Menck, Filippo Rosselli, Laurianne Drieu La Rochelle, Caroline Robert, Flore Sicre De Fontbrune, Marie Sébert, Thierry Leblanc, Patricia KannoucheStéphane De Botton, Eric Solary, Jean Soulier

Résultats de recherche: Contribution à un journal › Letter › Revue par des pairs

34 Citations (Scopus)

langue originale	Anglais
Pages (de - à)	2718-2724
Nombre de pages	7
journal	Blood
Volume	133
Numéro de publication	25
Les DOIs	https://doi.org/10.1182/blood-2019-01-895698
état	Publié - 20 juin 2019

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10.1182/blood-2019-01-895698

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Sarasin, A., Quentin, S., Droin, N., Sahbatou, M., Saada, V., Auger, N., Boursin, Y., Dessen, P., Raimbault, A., Asnafi, V., Schmutz, J. L., Taïeb, A., Menck, C. F. M., Rosselli, F., La Rochelle, L. D., Robert, C., De Fontbrune, F. S., Sébert, M., Leblanc, T., ... Soulier, J. (2019). Familial predisposition to TP53/complex karyotype MDS and leukemia in DNA repair-deficient xeroderma pigmentosum. Blood, 133(25), 2718-2724. https://doi.org/10.1182/blood-2019-01-895698

@article{0a05f99976234e40898bc4a4a7794d5f,

title = "Familial predisposition to TP53/complex karyotype MDS and leukemia in DNA repair-deficient xeroderma pigmentosum",

author = "Alain Sarasin and Samuel Quentin and Nathalie Droin and Mourad Sahbatou and V{\'e}ronique Saada and Nathalie Auger and Yannick Boursin and Philippe Dessen and Anna Raimbault and Vahid Asnafi and Schmutz, {Jean Luc} and Alain Ta{\"i}eb and Menck, {Carlos F.M.} and Filippo Rosselli and {La Rochelle}, {Laurianne Drieu} and Caroline Robert and {De Fontbrune}, {Flore Sicre} and Marie S{\'e}bert and Thierry Leblanc and Patricia Kannouche and {De Botton}, St{\'e}phane and Eric Solary and Jean Soulier",

note = "Funding Information: Part of this work was supported by the “Association des Enfants de La Lune” (Bellegarde sur Valserine, France) (A.S.), the European Research Council St Grant Consolidator #311660, the ANR-10-IBHU-0002 Saint-Louis Institute program, and the Programme d{\textquoteright}Action Int{\'e}gr{\'e}e de Recherche CONECT-AML (Collaborative Network on research for children and teenagers with AML) INCa-ARC-LIGUE_11905 (J.S.). Funding Information: The authors are very thankful to the physicians who took care of some of these patients with XP: C. Blanchet-Bardon, M. F. Avril, S. Hadj-Rabia, and R. Itzykson from Paris, France, and L. Schirmer (Nancy, France), C. Hardy (Vaison-la-Romaine, France), J. F. Stalder (Nantes, France), L. Sutton and J. Lejeune (Tours, France), G. Michel (Marseille), and M. Beylot-Barry (Bordeaux, France). The authors are also thankful to I. Plo (Villejuif, France), D. Stoppa-Lyonnet (Paris, France), and A. Remenieras, M. Lafage-Pochitaloff and I. Arnoux (Marseille, France) for their sequence analysis and helpful discussion. The authors are thankful to J. C. Ehrhart (Villejuif) for critical reading of the manuscript. Part of this work was supported by the ?Association des Enfants de La Lune? (Bellegarde sur Valserine, France) (A.S.), the European Research Council St Grant Consolidator #311660, the ANR-10-IBHU-0002 Saint-Louis Institute program, and the Programme d?Action Int?gr?e de Recherche CONECT-AML (Collaborative Network on research for children and teenagers with AML) INCa-ARC-LIGUE_11905 (J.S.).",

year = "2019",

month = jun,

day = "20",

doi = "10.1182/blood-2019-01-895698",

language = "English",

volume = "133",

pages = "2718--2724",

journal = "Blood",

issn = "0006-4971",

number = "25",

}

Sarasin, A, Quentin, S, Droin, N, Sahbatou, M, Saada, V, Auger, N, Boursin, Y, Dessen, P, Raimbault, A, Asnafi, V, Schmutz, JL, Taïeb, A, Menck, CFM, Rosselli, F, La Rochelle, LD, Robert, C, De Fontbrune, FS, Sébert, M, Leblanc, T, Kannouche, P, De Botton, S, Solary, E & Soulier, J 2019, 'Familial predisposition to TP53/complex karyotype MDS and leukemia in DNA repair-deficient xeroderma pigmentosum', Blood, VOL. 133, Numéro 25, p. 2718-2724. https://doi.org/10.1182/blood-2019-01-895698

TY - JOUR

T1 - Familial predisposition to TP53/complex karyotype MDS and leukemia in DNA repair-deficient xeroderma pigmentosum

AU - Sarasin, Alain

AU - Quentin, Samuel

AU - Droin, Nathalie

AU - Sahbatou, Mourad

AU - Saada, Véronique

AU - Auger, Nathalie

AU - Boursin, Yannick

AU - Dessen, Philippe

AU - Raimbault, Anna

AU - Asnafi, Vahid

AU - Schmutz, Jean Luc

AU - Taïeb, Alain

AU - Menck, Carlos F.M.

AU - Rosselli, Filippo

AU - La Rochelle, Laurianne Drieu

AU - Robert, Caroline

AU - De Fontbrune, Flore Sicre

AU - Sébert, Marie

AU - Leblanc, Thierry

AU - Kannouche, Patricia

AU - De Botton, Stéphane

AU - Solary, Eric

AU - Soulier, Jean

N1 - Funding Information: Part of this work was supported by the “Association des Enfants de La Lune” (Bellegarde sur Valserine, France) (A.S.), the European Research Council St Grant Consolidator #311660, the ANR-10-IBHU-0002 Saint-Louis Institute program, and the Programme d’Action Intégrée de Recherche CONECT-AML (Collaborative Network on research for children and teenagers with AML) INCa-ARC-LIGUE_11905 (J.S.). Funding Information: The authors are very thankful to the physicians who took care of some of these patients with XP: C. Blanchet-Bardon, M. F. Avril, S. Hadj-Rabia, and R. Itzykson from Paris, France, and L. Schirmer (Nancy, France), C. Hardy (Vaison-la-Romaine, France), J. F. Stalder (Nantes, France), L. Sutton and J. Lejeune (Tours, France), G. Michel (Marseille), and M. Beylot-Barry (Bordeaux, France). The authors are also thankful to I. Plo (Villejuif, France), D. Stoppa-Lyonnet (Paris, France), and A. Remenieras, M. Lafage-Pochitaloff and I. Arnoux (Marseille, France) for their sequence analysis and helpful discussion. The authors are thankful to J. C. Ehrhart (Villejuif) for critical reading of the manuscript. Part of this work was supported by the ?Association des Enfants de La Lune? (Bellegarde sur Valserine, France) (A.S.), the European Research Council St Grant Consolidator #311660, the ANR-10-IBHU-0002 Saint-Louis Institute program, and the Programme d?Action Int?gr?e de Recherche CONECT-AML (Collaborative Network on research for children and teenagers with AML) INCa-ARC-LIGUE_11905 (J.S.).

PY - 2019/6/20

Y1 - 2019/6/20

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U2 - 10.1182/blood-2019-01-895698

DO - 10.1182/blood-2019-01-895698

M3 - Letter

C2 - 30914417

AN - SCOPUS:85068361613

SN - 0006-4971

VL - 133

SP - 2718

EP - 2724

JO - Blood

JF - Blood

IS - 25

ER -