共 25 条
[1]
Clinical phenotype of germline RUNX1 haploinsufficiency:: from point mutations to large genomic deletions
[J].
Beri-Dexheimer, Mylene
;
Latger-Cannard, Veronique
;
Philippe, Christophe
;
Bonnet, Celine
;
Chambon, Pascal
;
Roth, Virginie
;
Gregoire, Marie-Jose
;
Bordigoni, Pierre
;
Lecompte, Thomas
;
Leheup, Bruno
;
Jonveaux, Philippe
.
EUROPEAN JOURNAL OF HUMAN GENETICS,
2008, 16 (08)
:1014-1018

Beri-Dexheimer, Mylene
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Nancy Brabois, Genet Lab, EA 4002, F-545111 Vandoeuvre Les Nancy, France CHU Nancy Brabois, Genet Lab, EA 4002, F-545111 Vandoeuvre Les Nancy, France

Latger-Cannard, Veronique
论文数: 0 引用数: 0
h-index: 0
机构:
Nancy Univ, INSERM, Hematol Lab, U734,CHU Nancy, Nancy, France CHU Nancy Brabois, Genet Lab, EA 4002, F-545111 Vandoeuvre Les Nancy, France

Philippe, Christophe
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Nancy Brabois, Genet Lab, EA 4002, F-545111 Vandoeuvre Les Nancy, France CHU Nancy Brabois, Genet Lab, EA 4002, F-545111 Vandoeuvre Les Nancy, France

Bonnet, Celine
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Nancy Brabois, Genet Lab, EA 4002, F-545111 Vandoeuvre Les Nancy, France CHU Nancy Brabois, Genet Lab, EA 4002, F-545111 Vandoeuvre Les Nancy, France

Chambon, Pascal
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Nancy Brabois, Genet Lab, EA 4002, F-545111 Vandoeuvre Les Nancy, France CHU Nancy Brabois, Genet Lab, EA 4002, F-545111 Vandoeuvre Les Nancy, France

Roth, Virginie
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Nancy Brabois, Genet Lab, EA 4002, F-545111 Vandoeuvre Les Nancy, France CHU Nancy Brabois, Genet Lab, EA 4002, F-545111 Vandoeuvre Les Nancy, France

Gregoire, Marie-Jose
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Nancy Brabois, Genet Lab, EA 4002, F-545111 Vandoeuvre Les Nancy, France CHU Nancy Brabois, Genet Lab, EA 4002, F-545111 Vandoeuvre Les Nancy, France

Bordigoni, Pierre
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Nancy, Serv Med Infantile 1, Nancy, France CHU Nancy Brabois, Genet Lab, EA 4002, F-545111 Vandoeuvre Les Nancy, France

Lecompte, Thomas
论文数: 0 引用数: 0
h-index: 0
机构:
Nancy Univ, INSERM, Hematol Lab, U734,CHU Nancy, Nancy, France CHU Nancy Brabois, Genet Lab, EA 4002, F-545111 Vandoeuvre Les Nancy, France

Leheup, Bruno
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Nancy, Serv Med Infantile 3 & Genet Clin, Nancy, France CHU Nancy Brabois, Genet Lab, EA 4002, F-545111 Vandoeuvre Les Nancy, France

Jonveaux, Philippe
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Nancy Brabois, Genet Lab, EA 4002, F-545111 Vandoeuvre Les Nancy, France CHU Nancy Brabois, Genet Lab, EA 4002, F-545111 Vandoeuvre Les Nancy, France
[2]
Dysmegakaryopoiesis of FPD/AML pedigrees with constitutional RUNX1 mutations is linked to myosin II deregulated expression
[J].
Bluteau, Dominique
;
Glembotsky, Ana C.
;
Raimbault, Anna
;
Balayn, Nathalie
;
Gilles, Laure
;
Rameau, Philippe
;
Nurden, Paquita
;
Alessi, Marie Christine
;
Debili, Najet
;
Vainchenker, William
;
Heller, Paula G.
;
Favier, Remi
;
Raslova, Hana
.
BLOOD,
2012, 120 (13)
:2708-2718

Bluteau, Dominique
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Paris Sud, Villejuif, France Inst Gustave Roussy, INSERM, UMR1009, F-94805 Villejuif, France

Glembotsky, Ana C.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Buenos Aires, Inst Invest Med Alfredo Lanari, Consejo Nacl Invest Cient & Tech, Buenos Aires, DF, Argentina Inst Gustave Roussy, INSERM, UMR1009, F-94805 Villejuif, France

Raimbault, Anna
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Paris Sud, Villejuif, France Inst Gustave Roussy, INSERM, UMR1009, F-94805 Villejuif, France

Balayn, Nathalie
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Paris Sud, Villejuif, France Inst Gustave Roussy, INSERM, UMR1009, F-94805 Villejuif, France

Gilles, Laure
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Paris Sud, Villejuif, France Inst Gustave Roussy, INSERM, UMR1009, F-94805 Villejuif, France

论文数: 引用数:
h-index:
机构:

Nurden, Paquita
论文数: 0 引用数: 0
h-index: 0
机构:
Hop Haut Leveque, Ctr Reference Pathol Plaquettaires, Pessac, France Inst Gustave Roussy, INSERM, UMR1009, F-94805 Villejuif, France

Alessi, Marie Christine
论文数: 0 引用数: 0
h-index: 0
机构:
Fac Med La Timone, INSERM, Marseille, France Inst Gustave Roussy, INSERM, UMR1009, F-94805 Villejuif, France

Debili, Najet
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Paris Sud, Villejuif, France Inst Gustave Roussy, INSERM, UMR1009, F-94805 Villejuif, France

Vainchenker, William
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Paris Sud, Villejuif, France Inst Gustave Roussy, INSERM, UMR1009, F-94805 Villejuif, France

Heller, Paula G.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Buenos Aires, Inst Invest Med Alfredo Lanari, Consejo Nacl Invest Cient & Tech, Buenos Aires, DF, Argentina Inst Gustave Roussy, INSERM, UMR1009, F-94805 Villejuif, France

Favier, Remi
论文数: 0 引用数: 0
h-index: 0
机构:
Hop Haut Leveque, Ctr Reference Pathol Plaquettaires, Pessac, France
Hop Trousseau, AP HP, Serv Hematol Biol, F-75571 Paris, France Inst Gustave Roussy, INSERM, UMR1009, F-94805 Villejuif, France

Raslova, Hana
论文数: 0 引用数: 0
h-index: 0
机构:
Inst Gustave Roussy, INSERM, UMR1009, F-94805 Villejuif, France
Univ Paris Sud, Villejuif, France Inst Gustave Roussy, INSERM, UMR1009, F-94805 Villejuif, France
[3]
Clinical and laboratory characteristics in congenital ANKRD26 mutation-associated thrombocytopenia: A detailed phenotypic study of a family
[J].
Botero, Juliana Perez
;
Chen, Dong
;
He, Rong
;
Viswanatha, David S.
;
Majerus, Julie A.
;
Coon, Lea M.
;
Nguyen, Phuong L.
;
Reichard, Karen K.
;
Oliveira, Jennifer L.
;
Tefferi, Ayalew
;
Gangat, Naseema
;
Pruthi, Rajiv K.
;
Patnaik, Mrinal M.
.
PLATELETS,
2016, 27 (07)
:712-715

Botero, Juliana Perez
论文数: 0 引用数: 0
h-index: 0
机构:
Mayo Clin, Div Hematol, Dept Med, Rochester, MN USA Mayo Clin, Div Hematol, Dept Med, Rochester, MN USA

Chen, Dong
论文数: 0 引用数: 0
h-index: 0
机构:
Mayo Clin, Special Coagulat Lab, Rochester, MN USA
Mayo Clin, Dept Lab Med & Pathol, Div Hematopathol, Rochester, MN USA Mayo Clin, Div Hematol, Dept Med, Rochester, MN USA

He, Rong
论文数: 0 引用数: 0
h-index: 0
机构:
Mayo Clin, Special Coagulat Lab, Rochester, MN USA
Mayo Clin, Dept Lab Med & Pathol, Div Hematopathol, Rochester, MN USA Mayo Clin, Div Hematol, Dept Med, Rochester, MN USA

Viswanatha, David S.
论文数: 0 引用数: 0
h-index: 0
机构:
Mayo Clin, Dept Lab Med & Pathol, Div Hematopathol, Rochester, MN USA Mayo Clin, Div Hematol, Dept Med, Rochester, MN USA

Majerus, Julie A.
论文数: 0 引用数: 0
h-index: 0
机构:
Mayo Clin, Special Coagulat Lab, Rochester, MN USA Mayo Clin, Div Hematol, Dept Med, Rochester, MN USA

Coon, Lea M.
论文数: 0 引用数: 0
h-index: 0
机构:
Mayo Clin, Special Coagulat Lab, Rochester, MN USA
Mayo Clin, Dept Lab Med & Pathol, Div Hematopathol, Rochester, MN USA Mayo Clin, Div Hematol, Dept Med, Rochester, MN USA

Nguyen, Phuong L.
论文数: 0 引用数: 0
h-index: 0
机构:
Mayo Clin, Dept Lab Med & Pathol, Div Hematopathol, Rochester, MN USA Mayo Clin, Div Hematol, Dept Med, Rochester, MN USA

Reichard, Karen K.
论文数: 0 引用数: 0
h-index: 0
机构:
Mayo Clin, Dept Lab Med & Pathol, Div Hematopathol, Rochester, MN USA Mayo Clin, Div Hematol, Dept Med, Rochester, MN USA

Oliveira, Jennifer L.
论文数: 0 引用数: 0
h-index: 0
机构:
Mayo Clin, Dept Lab Med & Pathol, Div Hematopathol, Rochester, MN USA Mayo Clin, Div Hematol, Dept Med, Rochester, MN USA

Tefferi, Ayalew
论文数: 0 引用数: 0
h-index: 0
机构:
Mayo Clin, Div Hematol, Dept Med, Rochester, MN USA Mayo Clin, Div Hematol, Dept Med, Rochester, MN USA

Gangat, Naseema
论文数: 0 引用数: 0
h-index: 0
机构:
Mayo Clin, Div Hematol, Dept Med, Rochester, MN USA Mayo Clin, Div Hematol, Dept Med, Rochester, MN USA

Pruthi, Rajiv K.
论文数: 0 引用数: 0
h-index: 0
机构:
Mayo Clin, Div Hematol, Dept Med, Rochester, MN USA
Mayo Clin, Special Coagulat Lab, Rochester, MN USA Mayo Clin, Div Hematol, Dept Med, Rochester, MN USA

Patnaik, Mrinal M.
论文数: 0 引用数: 0
h-index: 0
机构:
Mayo Clin, Div Hematol, Dept Med, Rochester, MN USA Mayo Clin, Div Hematol, Dept Med, Rochester, MN USA
[4]
INHERITED PLATELET-STORAGE POOL DEFICIENCY ASSOCIATED WITH A HIGH-INCIDENCE OF ACUTE MYELOID-LEUKEMIA
[J].
GERRARD, JM
;
ISRAELS, ED
;
BISHOP, AJ
;
SCHROEDER, ML
;
BEATTIE, LL
;
MCNICOI, A
;
ISRAELS, SJ
;
WALZ, D
;
GREENBERG, AH
;
RAY, M
;
ISRAELS, LG
.
BRITISH JOURNAL OF HAEMATOLOGY,
1991, 79 (02)
:246-255

GERRARD, JM
论文数: 0 引用数: 0
h-index: 0
机构: UNIV MANITOBA,DEPT MED,WINNIPEG R3E 0V9,MANITOBA,CANADA

ISRAELS, ED
论文数: 0 引用数: 0
h-index: 0
机构: UNIV MANITOBA,DEPT MED,WINNIPEG R3E 0V9,MANITOBA,CANADA

BISHOP, AJ
论文数: 0 引用数: 0
h-index: 0
机构: UNIV MANITOBA,DEPT MED,WINNIPEG R3E 0V9,MANITOBA,CANADA

SCHROEDER, ML
论文数: 0 引用数: 0
h-index: 0
机构: UNIV MANITOBA,DEPT MED,WINNIPEG R3E 0V9,MANITOBA,CANADA

BEATTIE, LL
论文数: 0 引用数: 0
h-index: 0
机构: UNIV MANITOBA,DEPT MED,WINNIPEG R3E 0V9,MANITOBA,CANADA

MCNICOI, A
论文数: 0 引用数: 0
h-index: 0
机构: UNIV MANITOBA,DEPT MED,WINNIPEG R3E 0V9,MANITOBA,CANADA

ISRAELS, SJ
论文数: 0 引用数: 0
h-index: 0
机构: UNIV MANITOBA,DEPT MED,WINNIPEG R3E 0V9,MANITOBA,CANADA

WALZ, D
论文数: 0 引用数: 0
h-index: 0
机构: UNIV MANITOBA,DEPT MED,WINNIPEG R3E 0V9,MANITOBA,CANADA

GREENBERG, AH
论文数: 0 引用数: 0
h-index: 0
机构: UNIV MANITOBA,DEPT MED,WINNIPEG R3E 0V9,MANITOBA,CANADA

RAY, M
论文数: 0 引用数: 0
h-index: 0
机构: UNIV MANITOBA,DEPT MED,WINNIPEG R3E 0V9,MANITOBA,CANADA

ISRAELS, LG
论文数: 0 引用数: 0
h-index: 0
机构: UNIV MANITOBA,DEPT MED,WINNIPEG R3E 0V9,MANITOBA,CANADA
[5]
High incidence of somatic mutations in the AML1/RUNX1 gene in myelodysplastic syndrome and low blast percentage myeloid leukemia with myelodysplasia
[J].
Harada, H
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Harada, Y
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Niimi, H
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Kyo, T
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Kimura, A
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Inaba, T
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BLOOD,
2004, 103 (06)
:2316-2324

Harada, H
论文数: 0 引用数: 0
h-index: 0
机构: Hiroshima Univ, Dept Mol Oncol, Res Inst Radiat Biol & Med, Minami Ku, Hiroshima 7348553, Japan

Harada, Y
论文数: 0 引用数: 0
h-index: 0
机构: Hiroshima Univ, Dept Mol Oncol, Res Inst Radiat Biol & Med, Minami Ku, Hiroshima 7348553, Japan

Niimi, H
论文数: 0 引用数: 0
h-index: 0
机构: Hiroshima Univ, Dept Mol Oncol, Res Inst Radiat Biol & Med, Minami Ku, Hiroshima 7348553, Japan

Kyo, T
论文数: 0 引用数: 0
h-index: 0
机构: Hiroshima Univ, Dept Mol Oncol, Res Inst Radiat Biol & Med, Minami Ku, Hiroshima 7348553, Japan

Kimura, A
论文数: 0 引用数: 0
h-index: 0
机构: Hiroshima Univ, Dept Mol Oncol, Res Inst Radiat Biol & Med, Minami Ku, Hiroshima 7348553, Japan

Inaba, T
论文数: 0 引用数: 0
h-index: 0
机构: Hiroshima Univ, Dept Mol Oncol, Res Inst Radiat Biol & Med, Minami Ku, Hiroshima 7348553, Japan
[6]
Diagnostic utility of light transmission platelet aggregometry: results from a prospective study of individuals referred for bleeding disorder assessments
[J].
Hayward, C. P. M.
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Pai, M.
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Liu, Y.
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Moffat, K. A.
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Seecharan, J.
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Webert, K. E.
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Cook, R. J.
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Heddle, N. M.
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JOURNAL OF THROMBOSIS AND HAEMOSTASIS,
2009, 7 (04)
:676-684

Hayward, C. P. M.
论文数: 0 引用数: 0
h-index: 0
机构:
McMaster Univ, Med Ctr, Dept Pathol & Mol Med, Hamilton, ON L8N 3Z5, Canada
McMaster Univ, Dept Med, Hamilton, ON L8N 3Z5, Canada
Hamilton Reg Lab Med Program, Hamilton, ON, Canada McMaster Univ, Med Ctr, Dept Pathol & Mol Med, Hamilton, ON L8N 3Z5, Canada

Pai, M.
论文数: 0 引用数: 0
h-index: 0
机构:
McMaster Univ, Dept Med, Hamilton, ON L8N 3Z5, Canada McMaster Univ, Med Ctr, Dept Pathol & Mol Med, Hamilton, ON L8N 3Z5, Canada

Liu, Y.
论文数: 0 引用数: 0
h-index: 0
机构:
McMaster Univ, Dept Med, Hamilton, ON L8N 3Z5, Canada McMaster Univ, Med Ctr, Dept Pathol & Mol Med, Hamilton, ON L8N 3Z5, Canada

Moffat, K. A.
论文数: 0 引用数: 0
h-index: 0
机构:
McMaster Univ, Dept Med, Hamilton, ON L8N 3Z5, Canada
Hamilton Reg Lab Med Program, Hamilton, ON, Canada McMaster Univ, Med Ctr, Dept Pathol & Mol Med, Hamilton, ON L8N 3Z5, Canada

Seecharan, J.
论文数: 0 引用数: 0
h-index: 0
机构:
Hamilton Reg Lab Med Program, Hamilton, ON, Canada McMaster Univ, Med Ctr, Dept Pathol & Mol Med, Hamilton, ON L8N 3Z5, Canada

Webert, K. E.
论文数: 0 引用数: 0
h-index: 0
机构:
McMaster Univ, Dept Med, Hamilton, ON L8N 3Z5, Canada
Hamilton Reg Lab Med Program, Hamilton, ON, Canada McMaster Univ, Med Ctr, Dept Pathol & Mol Med, Hamilton, ON L8N 3Z5, Canada

Cook, R. J.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Waterloo, Dept Stat & Actuarial Sci, Waterloo, ON N2L 3G1, Canada McMaster Univ, Med Ctr, Dept Pathol & Mol Med, Hamilton, ON L8N 3Z5, Canada

Heddle, N. M.
论文数: 0 引用数: 0
h-index: 0
机构:
McMaster Univ, Dept Med, Hamilton, ON L8N 3Z5, Canada McMaster Univ, Med Ctr, Dept Pathol & Mol Med, Hamilton, ON L8N 3Z5, Canada
[7]
Linkage of a familial platelet disorder with a propensity to develop myeloid malignancies to human chromosome 21q22.1-22.2
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Ho, CY
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Otterud, B
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Legare, RD
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Varvil, T
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Saxena, R
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DeHart, DB
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Kohler, SE
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Aster, JC
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Dowton, SB
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Li, FP
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Leppert, M
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Gilliland, DG
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BLOOD,
1996, 87 (12)
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Ho, CY
论文数: 0 引用数: 0
h-index: 0
机构: HARVARD UNIV,BRIGHAM & WOMENS HOSP,SCH MED,DEPT MED,DIV HEMATOL ONCOL,BOSTON,MA 02115

Otterud, B
论文数: 0 引用数: 0
h-index: 0
机构: HARVARD UNIV,BRIGHAM & WOMENS HOSP,SCH MED,DEPT MED,DIV HEMATOL ONCOL,BOSTON,MA 02115

Legare, RD
论文数: 0 引用数: 0
h-index: 0
机构: HARVARD UNIV,BRIGHAM & WOMENS HOSP,SCH MED,DEPT MED,DIV HEMATOL ONCOL,BOSTON,MA 02115

Varvil, T
论文数: 0 引用数: 0
h-index: 0
机构: HARVARD UNIV,BRIGHAM & WOMENS HOSP,SCH MED,DEPT MED,DIV HEMATOL ONCOL,BOSTON,MA 02115

Saxena, R
论文数: 0 引用数: 0
h-index: 0
机构: HARVARD UNIV,BRIGHAM & WOMENS HOSP,SCH MED,DEPT MED,DIV HEMATOL ONCOL,BOSTON,MA 02115

DeHart, DB
论文数: 0 引用数: 0
h-index: 0
机构: HARVARD UNIV,BRIGHAM & WOMENS HOSP,SCH MED,DEPT MED,DIV HEMATOL ONCOL,BOSTON,MA 02115

Kohler, SE
论文数: 0 引用数: 0
h-index: 0
机构: HARVARD UNIV,BRIGHAM & WOMENS HOSP,SCH MED,DEPT MED,DIV HEMATOL ONCOL,BOSTON,MA 02115

Aster, JC
论文数: 0 引用数: 0
h-index: 0
机构: HARVARD UNIV,BRIGHAM & WOMENS HOSP,SCH MED,DEPT MED,DIV HEMATOL ONCOL,BOSTON,MA 02115

Dowton, SB
论文数: 0 引用数: 0
h-index: 0
机构: HARVARD UNIV,BRIGHAM & WOMENS HOSP,SCH MED,DEPT MED,DIV HEMATOL ONCOL,BOSTON,MA 02115

Li, FP
论文数: 0 引用数: 0
h-index: 0
机构: HARVARD UNIV,BRIGHAM & WOMENS HOSP,SCH MED,DEPT MED,DIV HEMATOL ONCOL,BOSTON,MA 02115

Leppert, M
论文数: 0 引用数: 0
h-index: 0
机构: HARVARD UNIV,BRIGHAM & WOMENS HOSP,SCH MED,DEPT MED,DIV HEMATOL ONCOL,BOSTON,MA 02115

Gilliland, DG
论文数: 0 引用数: 0
h-index: 0
机构: HARVARD UNIV,BRIGHAM & WOMENS HOSP,SCH MED,DEPT MED,DIV HEMATOL ONCOL,BOSTON,MA 02115
[8]
Oncogenic potential of the RUNX gene family: 'Overview'
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Ito, Y
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ONCOGENE,
2004, 23 (24)
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Ito, Y
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h-index: 0
机构: Natl Univ Singapore, Inst Mol & Cell Biol, Singapore 117609, Singapore
[9]
The RUNX family: developmental regulators in cancer
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Ito, Yoshiaki
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Bae, Suk-Chul
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Chuang, Linda Shyue Huey
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NATURE REVIEWS CANCER,
2015, 15 (02)
:81-95

Ito, Yoshiaki
论文数: 0 引用数: 0
h-index: 0
机构:
Natl Univ Singapore, Ctr Translat Med, Canc Sci Inst Singapore, Singapore 117599, Singapore Natl Univ Singapore, Ctr Translat Med, Canc Sci Inst Singapore, Singapore 117599, Singapore

Bae, Suk-Chul
论文数: 0 引用数: 0
h-index: 0
机构:
Chungbuk Natl Univ, Dept Biochem, Sch Med, Chongju 361763, South Korea
Chungbuk Natl Univ, Inst Tumour Res, Chongju 361763, South Korea Natl Univ Singapore, Ctr Translat Med, Canc Sci Inst Singapore, Singapore 117599, Singapore

Chuang, Linda Shyue Huey
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h-index: 0
机构:
Natl Univ Singapore, Ctr Translat Med, Canc Sci Inst Singapore, Singapore 117599, Singapore Natl Univ Singapore, Ctr Translat Med, Canc Sci Inst Singapore, Singapore 117599, Singapore
[10]
The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data
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Koehler, Sebastian
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Doelken, Sandra C.
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Mungall, Christopher J.
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Bauer, Sebastian
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Firth, Helen V.
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Bailleul-Forestier, Isabelle
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Black, Graeme C. M.
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Brown, Danielle L.
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Brudno, Michael
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Campbell, Jennifer
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FitzPatrick, David R.
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Eppig, Janan T.
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Jackson, Andrew P.
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Freson, Kathleen
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Girdea, Marta
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Helbig, Ingo
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Hurst, Jane A.
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Jaehn, Johanna
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Jackson, Laird G.
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Kelly, Anne M.
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Ledbetter, David H.
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Mansour, Sahar
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Martin, Christa L.
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Moss, Celia
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Mumford, Andrew
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Ouwehand, Willem H.
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Park, Soo-Mi
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Riggs, Erin Rooney
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Scott, Richard H.
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Sisodiya, Sanjay
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Van Vooren, Steven
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Wapner, Ronald J.
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Wilkie, Andrew O. M.
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Wright, Caroline F.
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Vulto-van Silfhout, Anneke T.
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de Leeuw, Nicole
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de Vries, Bert B. A.
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Washingthon, Nicole L.
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Smith, Cynthia L.
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Westerfield, Monte
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Schofield, Paul
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Ruef, Barbara J.
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NUCLEIC ACIDS RESEARCH,
2014, 42 (D1)
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Koehler, Sebastian
论文数: 0 引用数: 0
h-index: 0
机构:
Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany
Charite, Berlin Brandenburg Ctr Regenerat Therapies, D-13353 Berlin, Germany Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Doelken, Sandra C.
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机构:
Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Mungall, Christopher J.
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机构:
Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Berkeley, CA 94720 USA Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Bauer, Sebastian
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机构:
Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Firth, Helen V.
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h-index: 0
机构:
Wellcome Trust Sanger Inst, Hinxton CB10 1SA, Cambs, England
Univ Cambridge, Addenbrookes Hosp, Dept Med Genet, Cambridge CB2 2QQ, England Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Bailleul-Forestier, Isabelle
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机构:
Univ Toulouse 3, Fac Chirurg Dent, CHU Toulouse, F-31062 Toulouse, France Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Black, Graeme C. M.
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机构:
Cent Manchester Univ Hosp NHS Fdn Trust, Manchester Acad Hlth Sci Ctr, Ctr Genom Med, Manchester, Lancs, England
Univ Manchester, MAHSC, Fac Med & Human Sci, Inst Human Dev,Ctr Genom Med, Manchester M13 9WL, Lancs, England Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Brown, Danielle L.
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机构:
Newcastle Univ, Inst Med Genet, Newcastle Upon Tyne NE1 3BZ, Tyne & Wear, England Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Brudno, Michael
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h-index: 0
机构:
Univ Toronto, Dept Comp Sci, Toronto, ON M5S 1A1, Canada
Hosp Sick Children, Ctr Computat Med, Toronto, ON M5G 1X8, Canada Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Campbell, Jennifer
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h-index: 0
机构:
Newcastle Univ, Inst Med Genet, Newcastle Upon Tyne NE1 3BZ, Tyne & Wear, England
Leeds Teaching Hosp NHS Trust, Dept Clin Genet, Leeds LS2 9NS, W Yorkshire, England Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

FitzPatrick, David R.
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机构:
Univ Edinburgh, MRC Inst Genet & Mol Med, MRC Human Genet Unit, Edinburgh EH4 2XU, Midlothian, Scotland Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Eppig, Janan T.
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机构:
Jackson Lab, Bar Harbor, ME 04609 USA Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Jackson, Andrew P.
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h-index: 0
机构:
Univ Edinburgh, MRC Inst Genet & Mol Med, MRC Human Genet Unit, Edinburgh EH4 2XU, Midlothian, Scotland Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Freson, Kathleen
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h-index: 0
机构:
Univ Leuven, Ctr Mol & Vasc Biol, Louvain, Belgium Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Girdea, Marta
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Toronto, Dept Comp Sci, Toronto, ON M5S 1A1, Canada
Hosp Sick Children, Ctr Computat Med, Toronto, ON M5G 1X8, Canada Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Helbig, Ingo
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机构:
Univ Med Ctr Schleswig Holstein, Dept Neuropediat, D-24105 Kiel, Germany Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Hurst, Jane A.
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h-index: 0
机构:
Great Ormond St Hosp Sick Children, NE Thames Genet Serv, London WC1N 3JH, England Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Jaehn, Johanna
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h-index: 0
机构:
Univ Med Ctr Schleswig Holstein, Dept Neuropediat, D-24105 Kiel, Germany Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Jackson, Laird G.
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h-index: 0
机构:
Drexel Univ, Coll Med, Philadelphia, PA 19102 USA Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Kelly, Anne M.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Cambridge, Dept Haematol, Cambridge CB2 0PT, England
NHS Blood & Transplant Cambridge, Cambridge CB2 0PT, England Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Ledbetter, David H.
论文数: 0 引用数: 0
h-index: 0
机构:
Geisinger Hlth Syst, Autism & Dev Med Inst, Danville, PA 17822 USA Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Mansour, Sahar
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h-index: 0
机构:
St Georges Healthcare NHS Trust, SW Thames Reg Genet Serv, London SW17 0RE, England Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Martin, Christa L.
论文数: 0 引用数: 0
h-index: 0
机构:
Geisinger Hlth Syst, Autism & Dev Med Inst, Danville, PA 17822 USA Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Moss, Celia
论文数: 0 引用数: 0
h-index: 0
机构:
Birmingham Childrens Hosp, Dept Dermatol, Birmingham, W Midlands, England Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Mumford, Andrew
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Bristol, Bristol Heart Inst, Bristol, Avon, England Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Ouwehand, Willem H.
论文数: 0 引用数: 0
h-index: 0
机构:
Wellcome Trust Sanger Inst, Hinxton CB10 1SA, Cambs, England
Univ Cambridge, Dept Haematol, Cambridge CB2 0PT, England
NHS Blood & Transplant Cambridge, Cambridge CB2 0PT, England Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Park, Soo-Mi
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h-index: 0
机构:
Univ Cambridge, Addenbrookes Hosp, Dept Med Genet, Cambridge CB2 2QQ, England Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Riggs, Erin Rooney
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h-index: 0
机构:
Geisinger Hlth Syst, Autism & Dev Med Inst, Danville, PA 17822 USA Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Scott, Richard H.
论文数: 0 引用数: 0
h-index: 0
机构:
Great Ormond St Hosp Sick Children, Dept Clin Genet, London, England
UCL Inst Child Hlth, Clin & Mol Genet Unit, London, England Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Sisodiya, Sanjay
论文数: 0 引用数: 0
h-index: 0
机构:
UCL Inst Neurol, Dept Clin & Expt Epilepsy, London, England Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Van Vooren, Steven
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机构:
Cartagenia, Louvain, Belgium Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Wapner, Ronald J.
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h-index: 0
机构:
Columbia Univ, Med Ctr, Dept Obstet & Gynecol, New York, NY 10032 USA Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Wilkie, Andrew O. M.
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h-index: 0
机构:
Univ Oxford, John Radcliffe Hosp, Weatherall Inst Mol Med, Oxford OX3 9DS, England Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Wright, Caroline F.
论文数: 0 引用数: 0
h-index: 0
机构:
Wellcome Trust Sanger Inst, Hinxton CB10 1SA, Cambs, England Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Vulto-van Silfhout, Anneke T.
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h-index: 0
机构:
Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

de Leeuw, Nicole
论文数: 0 引用数: 0
h-index: 0
机构:
Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

de Vries, Bert B. A.
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h-index: 0
机构:
Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Washingthon, Nicole L.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Berkeley, CA 94720 USA Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Smith, Cynthia L.
论文数: 0 引用数: 0
h-index: 0
机构:
Jackson Lab, Bar Harbor, ME 04609 USA Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Westerfield, Monte
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h-index: 0
机构:
Univ Oregon, ZFIN, Eugene, OR 97403 USA Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Schofield, Paul
论文数: 0 引用数: 0
h-index: 0
机构:
Jackson Lab, Bar Harbor, ME 04609 USA
Dept Physiol Dev & Neurosci, Cambridge CB2 3EG, England Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Ruef, Barbara J.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Oregon, ZFIN, Eugene, OR 97403 USA Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Gkoutos, Georgios V.
论文数: 0 引用数: 0
h-index: 0
机构:
Aberystwyth Univ, Dept Comp Sci, Aberystwyth SY23 3DB, Ceredigion, Wales Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

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Smedley, Damian
论文数: 0 引用数: 0
h-index: 0
机构:
Wellcome Trust Sanger Inst, Hinxton CB10 1SA, Cambs, England Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Lewis, Suzanna E.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Berkeley, CA 94720 USA Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany

Robinson, Peter N.
论文数: 0 引用数: 0
h-index: 0
机构:
Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany
Charite, Berlin Brandenburg Ctr Regenerat Therapies, D-13353 Berlin, Germany
Max Planck Inst Mol Genet, D-14195 Berlin, Germany Charite, Inst Med Genet & Human Genet, D-13353 Berlin, Germany