Q. Waisfisz
发表
Jaana M. Hartikainen,
A. Hofman,
A. Uitterlinden,
2013,
Nature Genetics.
Jeroen F. J. Laros,
R. Pfundt,
G. Thijs,
2019,
Human mutation.
J. D. de Vries,
F. Baas,
Q. Waisfisz,
2014,
European Journal of Human Genetics.
Hans Joenje,
Edward A. Fox,
Quinten Waisfisz,
2002,
Science.
Q. Waisfisz,
F. Kruyt,
H. Joenje,
1997,
Blood.
Jaana M. Hartikainen,
S. Cross,
M. Beckmann,
2014,
PloS one.
Gary D Bader,
Jaana M. Hartikainen,
Jeffery M. Meyer,
2017,
Nature.
Jeffery M. Meyer,
Richard T. Barfield,
Jack A. Taylor,
2018,
Nature Genetics.
A. W. van der Vaart,
A. van der Vaart,
H. Meijers-Heijboer,
2011,
Journal of Medical Genetics.
Henning Gall,
Andrea Olschewski,
Horst Olschewski,
2018,
Nature Communications.
Quinten Waisfisz,
M. Nelen,
Q. Waisfisz,
2013,
Human mutation.
D. Jong,
F. Baas,
M. Reinders,
2020
.
Edwin Cuppen,
Marcel Nelen,
Wilfred F J van IJcken,
2015,
European Journal of Human Genetics.
Connie,
M. Warmoes,
Q. Waisfisz,
2012
.
Marc Warmoes,
Jos Jonkers,
Thang V Pham,
2012,
Molecular & Cellular Proteomics.
Mahshid S. Azamian,
J. Rosenfeld,
S. Lalani,
2020,
American journal of human genetics.
Q. Waisfisz,
2008
.
Q. Waisfisz,
D. Reinhardt,
G. Schuurhuis,
2006,
Leukemia.
Q. Waisfisz,
F. Kruyt,
H. Joenje,
1999,
Proceedings of the National Academy of Sciences of the United States of America.
Q. Waisfisz,
P. Postmus,
E. Thunnissen,
2012,
Familial Cancer.
Jane E. Carpenter,
Daniel J. Park,
Gary K. Chen,
2012,
Human molecular genetics.
Q. Waisfisz,
G. Schuurhuis,
J. Janssen,
2004,
Leukemia.
E. Bertini,
M. Tarnopolsky,
C. Catsman-Berrevoets,
2015,
Annals of clinical and translational neurology.
Q. Waisfisz,
G. Schuurhuis,
G. Ossenkoppele,
2000
.
Q. Waisfisz,
G. Schuurhuis,
G. Ossenkoppele,
2000,
British journal of haematology.
B. Bonanni,
T. Rebbeck,
J. Benítez,
2011,
British Journal of Cancer.
J. Martens,
A. Broeks,
M. Schmidt,
2013,
European journal of cancer.
Q. Waisfisz,
E. Gizewski,
S. Boesch,
2018,
neurogenetics.
Q. Waisfisz,
H. Niessen,
M. S. van der Knaap,
2016,
Neurology.
Q. Waisfisz,
M. S. van der Knaap,
R. Neeleman,
2016,
Neurology.
D. de Jong,
F. Baas,
M. Reinders,
2020,
Leukemia.
D. de Jong,
F. Baas,
M. Reinders,
2019,
bioRxiv.
D. de Jong,
F. Baas,
M. Reinders,
2019,
Leukemia.
Lisa J. Martin,
Ferhaan Ahmad,
W. Ouwehand,
2018,
bioRxiv.
C. Mathew,
Q. Waisfisz,
H. Hoehn,
2003,
Experimental cell research.
E. Liebau,
P. Pouwels,
Q. Waisfisz,
2021,
Neuropediatrics.
E. Bertini,
A. Vanderver,
Q. Waisfisz,
2017,
Neurology.
G. M. Taylor,
J. Clayton-Smith,
Q. Waisfisz,
2005,
Genes, chromosomes & cancer.
N. Alon,
C. Mathew,
Q. Waisfisz,
2000,
American journal of human genetics.
Lisa J. Martin,
Ferhaan Ahmad,
W. Ouwehand,
2018,
bioRxiv.
Gary D Bader,
C. Gieger,
W. Maier,
2022,
Cancers.
Masa Umicevic Mirkov,
M. Hurles,
R. Zwart,
2020,
Genetics in Medicine.
Q. Waisfisz,
J. V. van Waesberghe,
P. Postmus,
2012,
Journal of the American Academy of Dermatology.
J. Rosenfeld,
S. Wells,
S. Mane,
2016,
American journal of human genetics.
Q. Waisfisz,
T. Rigter,
A. Tibben,
2011
.
Jianxin Shi,
Daniel F. Schmidt,
Nazneen Rahman,
2014,
Cancer Epidemiology, Biomarkers & Prevention.
Q. Waisfisz,
M. Weiss,
J. Bierau,
2015,
Annals of neurology.
Q. Waisfisz,
D. Micha,
I. B. Mathijssen,
2018,
American journal of medical genetics. Part A.
Q. Waisfisz,
N. Nanninga,
M. Aarsman,
1995,
Journal of bacteriology.
A. Hofman,
A. Uitterlinden,
B. Wirth,
2014
.
Q. Waisfisz,
W. Kamphorst,
G. Scheper,
2005,
Journal of neuropathology and experimental neurology.
J. Berkhof,
Q. Waisfisz,
M. Heinrich,
2009,
Haematologica.
Q. Waisfisz,
T. D. de Gruijl,
G. Ossenkoppele,
2008,
British journal of haematology.
Q. Waisfisz,
G. Ossenkoppele,
S. Kipriyanov,
2006
.
Q. Waisfisz,
G. Ossenkoppele,
T. Westers,
2006,
Leukemia.
Henk M. W. Verheul,
Q. Waisfisz,
H. Meijers-Heijboer,
2013,
Human mutation.
Loris,
Fiona,
Meindl,
2012
.
C. Mathew,
Q. Waisfisz,
R. Gibson,
1999,
Nature Genetics.
B. Tazón-Vega,
Q. Waisfisz,
G. Santen,
2021,
Frontiers in Physiology.
E. Zackai,
H. Hakonarson,
H. Brunner,
2022,
HGG advances.
Q. Waisfisz,
H. Joenje,
2006
.
Q. Waisfisz,
P. Postmus,
E. Thunnissen,
2013,
Familial Cancer.
Q. Waisfisz,
J. M. van de Kamp,
M. Finken,
2022,
Clinical genetics.
Q. Waisfisz,
G. Ossenkoppele,
T. Westers,
2006,
Leukemia.
G. Pals,
Q. Waisfisz,
H. Meijers-Heijboer,
2020,
American journal of human genetics.
G. Pals,
Q. Waisfisz,
A. Medhurst,
2004,
Leukemia.
C. Mathew,
Q. Waisfisz,
A. D’Andrea,
2003,
British journal of haematology.
Keith W. Muir,
William J. Astle,
Mark I. McCarthy,
2020,
Nature.
Q. Waisfisz,
P. Heutink,
M. Knaap,
2013,
Brain : a journal of neurology.
Hans Joenje,
Johan P. de Winter,
Christopher G. Mathew,
2000,
Nature Genetics.
Hans Joenje,
Johan P. de Winter,
Quinten Waisfisz,
1998,
Nature Genetics.
Q. Waisfisz,
G. Schuurhuis,
G. Ossenkoppele,
2005,
Clinical Cancer Research.
Lisa T. Emrick,
Michael F. Wangler,
J. Rosenfeld,
2019,
Nature Communications.
S. Nelson,
P. Kwok,
W. Grody,
2016,
npj Genomic Medicine.
C. Mathew,
G. Pals,
Q. Waisfisz,
2005,
Nature Genetics.
Patrick Neven,
Peter Kraft,
Nazneen Rahman,
2015
.
Patrick Neven,
Michael Jones,
Wei Lu,
2013,
Nature Genetics.
C. Bishop,
Q. Waisfisz,
Weidong Wang,
2003,
Nature Genetics.
G. Gyapay,
A. Smahi,
C. Bodemer,
2017,
Nature Medicine.
Peter Devilee,
Alfons Meindl,
Lesley McGuffog,
2010,
Breast Cancer Research.
Q. Waisfisz,
H. Meijers-Heijboer,
Maarten Massink,
2015
.
M. Smid,
J. Martens,
Q. Waisfisz,
2019,
Clinical Cancer Research.
P. Striano,
B. Wirth,
Q. Waisfisz,
2018,
American journal of human genetics.
Enhanced MAPK1 Function Causes a Neurodevelopmental Disorder within the RASopathy Clinical Spectrum.
W. Chung,
Q. Waisfisz,
B. Gelb,
2020,
American journal of human genetics.
Q. Waisfisz,
K. Odunsi,
R. Dicioccio,
2013,
Genes & cancer.
R. Hochstenbach,
Q. Waisfisz,
R. Person,
2019,
American journal of medical genetics. Part A.
J. Graham,
Q. Waisfisz,
D. Wieczorek,
2019,
Brain : a journal of neurology.
J. Martens,
Q. Waisfisz,
H. Meijers-Heijboer,
2015,
BMC Cancer.
J. Soulier,
Q. Waisfisz,
D. Stoppa-Lyonnet,
2011,
The Journal of clinical investigation.
J. Foekens,
A. Sieuwerts,
M. Smid,
2015,
Molecular oncology.
Q. Waisfisz,
A. D’Andrea,
M. Sasaki,
2003,
Cancer research.
Q. Waisfisz,
K. J. Patel,
A. Medhurst,
2004,
Journal of Biological Chemistry.
C. Mathew,
Q. Waisfisz,
A. Medhurst,
2001,
Human molecular genetics.
Q. Waisfisz,
F. Kruyt,
H. Joenje,
2000,
Human molecular genetics.
D. de Jong,
R. Hennekam,
P. Wesseling,
2018,
American journal of medical genetics. Part A.
Michael Jones,
Nazneen Rahman,
Daniel J. Park,
2012,
Nature Genetics.
C. Mathew,
Q. Waisfisz,
H. Joenje,
2004,
Blood.
C. Mathew,
Q. Waisfisz,
A. D’Andrea,
2000,
American journal of human genetics.
C. Mathew,
Q. Waisfisz,
R. Wegner,
1999,
American journal of human genetics.
J. Schouten,
Q. Waisfisz,
N. Ameziane,
2005,
Nucleic acids research.
Q. Waisfisz,
M. Weiss,
G. Salomons,
2021,
Molecular genetics & genomic medicine.
Lisa J. Martin,
Keith A. Marsolo,
Ferhaan Ahmad,
2018,
bioRxiv.
C. Mathew,
G. Pals,
Q. Waisfisz,
2007,
Cellular oncology : the official journal of the International Society for Cellular Oncology.
R. Wolthuis,
Wouter van Zon,
Q. Waisfisz,
2009,
PloS one.
E. Jabs,
Q. Waisfisz,
H. Kayserili,
2005,
Nature Genetics.
Q. Waisfisz,
Johnson M Liu,
H. Joenje,
2002,
BMC blood disorders.
S. Cross,
M. Beckmann,
P. Fasching,
2022
.
William E. Byrd,
Gabor T. Marth,
David R. Murdock,
2020,
Genetics in Medicine.
M. Smid,
Q. Waisfisz,
H. Meijers-Heijboer,
2015
.
Q. Waisfisz,
M. Cornel,
P. Borry,
2013,
Human mutation.
T. Pandita,
I. Thiffault,
G. B. Schaefer,
2019,
The Journal of clinical investigation.
Michael Jones,
Julian Peto,
Thomas Brüning,
2016,
Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers.
Mads Thomassen,
Nina Ditsch,
Dieter Niederacher,
2009,
Human molecular genetics.
H. Meijers-Heijboer,
Q. Waisfisz,
E. Sistermans,
2014,
European journal of medical genetics.
H. Meijers-Heijboer,
Q. Waisfisz,
H. Meijers-Heijboer,
2011,
Breast Cancer Research and Treatment.
Q. Waisfisz,
T. Rigter,
L. Henneman,
2013,
Clinical genetics.
H. Hakonarson,
J. A. Taylor,
H. Brunner,
2021,
medRxiv.
P. Pouwels,
Q. Waisfisz,
R. Rodenburg,
2014,
Annals of neurology.
Q. Waisfisz,
D. Reinhardt,
C. Zwaan,
2008,
Cellular oncology : the official journal of the International Society for Cellular Oncology.
R. Wolthuis,
M. Speicher,
Q. Waisfisz,
2022,
Science advances.
William J. Astle,
Sri V. V. Deevi,
Kenneth G. C. Smith,
2020,
Nature.
R. Pfundt,
D. Baralle,
I. Thiffault,
2022,
American journal of human genetics.
Marc Vidal,
Dieter Niederacher,
Roderic Guigó,
2011,
PLoS biology.
A. Hofman,
A. Uitterlinden,
B. Wirth,
2013,
The New England journal of medicine.
R. Taft,
Q. Waisfisz,
R. Rodenburg,
2019,
Neurology.
I. Thiffault,
B. Coulombe,
B. Weschke,
2018,
American journal of human genetics.
M. Reinders,
Q. Waisfisz,
E. Sistermans,
2017,
European Journal of Human Genetics.
J. Berkhof,
J. Schouten,
Q. Waisfisz,
2007,
Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
Jane E. Carpenter,
Daniel J. Park,
Gary K. Chen,
2012,
Human molecular genetics.
Q. Waisfisz,
A. Medhurst,
H. Joenje,
2006,
Mutation research.
Quinten Waisfisz,
Johannes Berkhof,
Abdellatif Errami,
2008,
Leukemia & lymphoma.
R. Hruban,
S. Kern,
G. Pals,
2003
.
A. Vanderver,
R. Schiffmann,
R. Taft,
2014,
Brain : a journal of neurology.
R. Taft,
Q. Waisfisz,
J. Crawford,
2017,
Brain : a journal of neurology.
A. Reymond,
R. Myers,
G. Cooper,
2022,
American journal of human genetics.
Jeffery M. Meyer,
Jack A. Taylor,
A. Whittemore,
2018,
International journal of epidemiology.
E. Kuipers,
Q. Waisfisz,
A. Wagner,
2011,
European Journal of Human Genetics.
V. Pankratz,
F. Couch,
T. Rebbeck,
2010
.
P. Pouwels,
Q. Waisfisz,
J. M. van de Kamp,
2023,
JIMD reports.
R. Wolthuis,
Q. Waisfisz,
P. Postmus,
2023,
Journal of Human Genetics.
Q. Waisfisz,
S. Julia,
D. Wieczorek,
2023,
European Journal of Human Genetics.
Golder N Wilson,
E. Roeder,
D. Horn,
2020,
Brain : a journal of neurology.
E. Kuipers,
Q. Waisfisz,
A. Wagner,
2012
.
Q. Waisfisz,
H. Meijers-Heijboer,
M. Adank,
2009,
Breast Cancer Research and Treatment.
Q. Waisfisz,
E. Boon,
E. L. van den Akker,
2020,
European Journal of Human Genetics.
J. Berkhof,
Q. Waisfisz,
G. Schuurhuis,
2011
.
Q. Waisfisz,
E. Gizewski,
S. Boesch,
2018,
neurogenetics.
Q. Waisfisz,
J. M. van de Kamp,
M. S. van der Knaap,
2015,
Neuropediatrics.
Henk M. W. Verheul,
Q. Waisfisz,
H. Meijers-Heijboer,
2014,
Human mutation.
J. Veltman,
E. Cuppen,
R. Hennekam,
2015,
European Journal of Human Genetics.
E. Bertini,
Q. Waisfisz,
M. Knaap,
2018
.
Masa Umicevic Mirkov,
M. Hurles,
R. Zwart,
2020,
Genetics in Medicine.
M. Kool,
Q. Waisfisz,
H. Meijers-Heijboer,
2010,
Pediatric blood & cancer.
L. Vissers,
R. Pfundt,
R. V. van Lingen,
2023,
European Journal of Pediatrics.
R. Leurs,
H. Mansvelder,
Maarten H. P. Kole,
2023,
Brain : a journal of neurology.
C. Mathew,
Q. Waisfisz,
H. Joenje,
2004,
Blood.
J. Schouten,
C. Mcelgunn,
Q. Waisfisz,
2004,
Leukemia.
P. Striano,
B. Wirth,
Q. Waisfisz,
2021,
American journal of human genetics.
P. Striano,
B. Wirth,
Q. Waisfisz,
2018,
American journal of human genetics.
P. Pouwels,
Q. Waisfisz,
R. Rodenburg,
2014,
Annals of neurology.
C. Mathew,
Q. Waisfisz,
H. Joenje,
2004,
Blood.
Q. Waisfisz,
T. D. de Gruijl,
G. Ossenkoppele,
2008,
British journal of haematology.
Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers.
F. Couch,
B. Bonanni,
J. Benítez,
2009,
Human molecular genetics.
B. Wirth,
G. Pals,
Q. Waisfisz,
2013,
The New England journal of medicine.
Q. Waisfisz,
P. Heutink,
M. Knaap,
2013,
Brain : a journal of neurology.
Q. Waisfisz,
K. J. Patel,
A. Medhurst,
2004,
Journal of Biological Chemistry.
N. Soranzo,
Q. Waisfisz,
M. Haimel,
2018,
Nature Communications.
Jaana M. Hartikainen,
Sandra L. Halverson,
A. Whittemore,
2015,
Nature Genetics.
M. Reinders,
Q. Waisfisz,
E. Sistermans,
2017,
European Journal of Human Genetics.
Q. Waisfisz,
T. Rigter,
L. Henneman,
2013,
Clinical genetics.
Marni J. Falk,
J. Rosenfeld,
S. Wells,
2016,
American journal of human genetics.