K. Heinimann
发表
O. Sieber,
I. Tomlinson,
K. Heinimann,
2003,
Nature Reviews Cancer.
Peter Devilee,
Florentia Fostira,
Riccardo Fodde,
2010,
Human mutation.
L. Lipton,
O. Sieber,
I. Tomlinson,
2003,
The Journal of pathology.
L. Terracciano,
C. Quintavalle,
D. Baumhoer,
2019,
Scientific Reports.
Raquel Seruca,
Rui Henrique,
Isabel Veiga,
2015,
British Journal of Cancer.
J. Jiricny,
G. Marra,
K. Heinimann,
2003,
The EMBO journal.
L. Terracciano,
P. Demougin,
C. Noppen,
2011,
PloS one.
W. Wasserman,
Judith G Hall,
J. Friedman,
2014,
Clinical genetics.
P. Chappuis,
L. Perey,
C. Monnerat,
2017
.
J. Jiricny,
I. Iaccarino,
G. Marra,
2005,
Cancer research.
E. Valtorta,
G. Marra,
S. Gillessen,
2008,
Familial Cancer.
P. Møller,
D. Evans,
A. Spigelman,
2013,
Familial Cancer.
P. Chappuis,
S. Wieser,
M. Katapodi,
2021,
Journal of Medical Genetics.
An alternative approach to establishing unbiased colorectal cancer risk estimation in Lynch syndrome
J. Houwing-Duistermaat,
David Evans,
S. Nikolaev,
2019,
Genetics in Medicine.
H. Simmen,
K. Heinimann,
M. Turina,
2013,
International Journal of Colorectal Disease.
J. Jiricny,
D. Ilencikova,
G. Marra,
2008,
Clinical chemistry.
L. Terracciano,
M. Heim,
K. Heinimann,
2014,
European journal of cancer.
B. Bonanni,
P. Møller,
E. Hovig,
2020,
Journal of clinical medicine.
P. Chappuis,
P. Hutter,
R. Scott,
1999
.
M. Baudis,
S. Girlando,
L. Messiaen,
2012,
Genes, chromosomes & cancer.
G. Marra,
K. Heinimann,
M. Plášilová,
2006,
Genes, chromosomes & cancer.
A. Viel,
J. Burn,
M. Greenblatt,
2006,
Clinical Cancer Research.
J. Jiricny,
E. Laczko,
G. Marra,
2011,
Familial Cancer.
P. Chappuis,
S. Merajver,
C. Monnerat,
2021,
Cancers.
An MLH1 haplotype is over-represented on chromosomes carrying an HNPCC predisposing mutation in MLH1
P. Hutter,
W. Foulkes,
I. Thiffault,
2002,
Journal of medical genetics.
P. Hutter,
W. Foulkes,
I. Thiffault,
2002
.
R. Herrmann,
C. Rochlitz,
J. Boulay,
2005,
Oncology reports.
R. Scott,
J. Buerstedde,
K. Heinimann,
1999,
Cancer.
Florian Engert,
Joachim Weischenfeldt,
Jan Smida,
2015,
Nature Communications.
E. Bertini,
M. Tosetti,
G. Cioni,
2009,
Human mutation.
M. Zavolan,
S. Kishore,
H. Altermatt,
2013
.
Aung Ko Win,
M. von Knebel Doeberitz,
B. Bonanni,
2021,
European journal of cancer.
Aung Ko Win,
P. Møller,
E. Hovig,
2019,
Genetics in Medicine.
Aung Ko Win,
M. von Knebel Doeberitz,
B. Bonanni,
2020,
Genetics in Medicine.
Aung Ko Win,
P. Møller,
E. Hovig,
2020,
Genetics in Medicine.
Aung Ko Win,
M. Kloor,
B. Bonanni,
2022,
Hereditary Cancer in Clinical Practice.
R. Scott,
U. Meyer,
K. Heinimann,
1997,
European journal of human genetics : EJHG.
K. Heinimann,
S. Elalaoui,
A. Sefiani,
2017,
BMC Medical Genetics.
Mauro Delorenzi,
Vincent Castella,
M. Delorenzi,
2012,
Neuro-oncology.
R. Scott,
K. Heinimann,
D. Bishop,
1997,
Human Genetics.
P. Chappuis,
C. Monnerat,
G. Fink,
2022,
Journal of personalized medicine.
K. Heinimann,
Nadira M'Rabet,
R. Moffat,
2013,
Genetics in Medicine.
N. Probst-Hensch,
P. Chappuis,
M. Katapodi,
2017,
JMIR research protocols.
O. Sieber,
P. Hutter,
A. Rowan,
2006,
Gut.
P. Hutter,
I. Tomlinson,
D. Ilencikova,
2015,
Human mutation.
P. Møller,
G. Capellá,
A. Lindblom,
2013,
Gut.
I. Tomlinson,
I. Christensen,
S. Bülow,
2010,
Colorectal disease : the official journal of the Association of Coloproctology of Great Britain and Ireland.
T. Kühne,
K. Heinimann,
J. Rischewski,
2009
.
K. Heinimann,
P. Miny,
S. Buechner,
2004,
Journal of Medical Genetics.
K. Heinimann,
J. Hammer,
D. Trachsel,
2007,
Journal of Perinatology.
S. Pascual-Pascual,
C. Barbot,
T. Coelho,
2008,
Clinical genetics.
L. Lipton,
O. Sieber,
I. Tomlinson,
2003,
Oncogene.
K. Heinimann,
2013,
Front. Oncol..
S. Gultekin,
D. Ross,
S. Fischer,
2017,
Journal of Neuro-Oncology.
David M. Thomas,
I. Tomlinson,
S. Bielack,
2020,
Journal of Medical Genetics.
M. Fussenegger,
A. Scherberich,
B. Heng,
2013,
Metabolic engineering.
Ville Mustonen,
Andrea Sottoriva,
Xiaowei Jiang,
2018,
Nature Ecology & Evolution.
J. Jiricny,
M. Cattaruzza,
G. Marra,
2001,
Proceedings of the National Academy of Sciences of the United States of America.
K. Heinimann,
Z. Dobbie,
H. Müller,
2000,
European journal of cancer.
K. Heinimann,
H. Müller,
Z. Dobbie,
1999,
Schweizerische medizinische Wochenschrift.
I. Tomlinson,
Jenny C. Taylor,
S. Leedham,
2012,
Nature Genetics.
H. Kehrer-Sawatzki,
L. Messiaen,
K. Wimmer,
2010,
Human mutation.
Josef Jiricny,
Giancarlo Marra,
J. Jiricny,
2005,
Gastroenterology.
D. Evans,
H. Järvinen,
M. Genuardi,
2020,
Genetics in Medicine.
P. Møller,
D. Evans,
A. Spigelman,
2014,
Familial Cancer.
J. Beckmann,
A. Pica,
C. Monnerat,
2011,
Familial Cancer.
S. Frank,
J. Schneider,
D. Fischer,
2014,
Neuromuscular Disorders.
S. Frank,
D. Fischer,
A. Fischmann,
2014,
Neuromuscular Disorders.
K. Heinimann,
P. Miny,
S. Tercanli,
2012,
Molecular Cytogenetics.
N. Probst-Hensch,
P. Chappuis,
Z. Ademi,
2019,
Public Health Genomics.
M. Kool,
H. Friedman,
J. Koster,
2012,
British Journal of Cancer.
P. Hutter,
K. Heinimann,
Claudine Rey Berthod,
2005,
Human Genetics.
Aung Ko Win,
M. von Knebel Doeberitz,
B. Bonanni,
2021,
Journal of clinical medicine.
H. Frick,
K. Heinimann,
A. Omlin,
2017,
ESMO Open.
O. Sieber,
I. Tomlinson,
K. Heinimann,
2005,
Seminars in cancer biology.
O. Sieber,
W. Bodmer,
I. Tomlinson,
2002,
Proceedings of the National Academy of Sciences of the United States of America.
P. Demougin,
K. Heinimann,
P. Miny,
2011,
Clinical genetics.
M. Roncalli,
S. Francisconi,
G. Ranzani,
2002,
Laboratory Investigation.
K. Heinimann,
P. Miny,
S. Tercanli,
2011,
Prenatal diagnosis.
J. Jiricny,
Jacob Sabates-Bellver,
E. Cattaneo,
2007
.
I. Varela,
S. Horswell,
J. Larkin,
2015,
Nature Communications.
K. Heinimann,
Z. Dobbie,
A. Russell,
2004,
European Journal of Human Genetics.
L. Lipton,
O. Sieber,
W. Bodmer,
2002,
Proceedings of the National Academy of Sciences of the United States of America.
H. Moch,
M. Montani,
T. Rudolph,
2010,
The American journal of surgical pathology.
S. Stoeckli,
D. Engeler,
I. Binet,
2014,
Oncology Research and Treatment.
K. Heinimann,
A. Russell,
M. Plášilová,
2003,
Recent results in cancer research. Fortschritte der Krebsforschung. Progres dans les recherches sur le cancer.
A. Huber,
C. Noppen,
K. Heinimann,
2009,
American journal of medical genetics. Part A.
L. Lipton,
L. Aaltonen,
O. Sieber,
2003,
The New England journal of medicine.
D. Bartholdi,
S. Hoeller,
T. Kühne,
2015,
European journal of haematology.
L. Terracciano,
F. Molinari,
M. Frattini,
2010,
International journal of cancer.
L. Mazzucchelli,
G. Singer,
L. Terracciano,
2009,
British Journal of Cancer.
L. Kappos,
P. Fuhr,
S. Rüegg,
2005,
Swiss medical weekly.
S. Tschudin,
C. Kunz,
G. Szinnai,
2011,
Fertility and sterility.
K. Scheffler,
O. Bieri,
M. Gloor,
2011,
Journal of Neurology.
G. Marra,
K. Heinimann,
D. Foernzler,
2001,
Cancer research.
G. Marra,
K. Heinimann,
D. Foernzler,
2001
.
Oliver Bieri,
Klaus Scheffler,
Arne Fischmann,
2011,
Journal of magnetic resonance imaging : JMRI.
K. Heinimann,
N. Gürtler,
M. Plášilová,
2006,
The Laryngoscope.
A. Huber,
K. Heinimann,
P. Miny,
2008,
American journal of medical genetics. Part A.
R. Scott,
M. Fried,
B. Müllhaupt,
1998,
Gut.
P. Møller,
G. Capellá,
A. Lindblom,
2010,
Familial Cancer.
P. Chappuis,
P. Hutter,
J. Luz,
2006,
International journal of cancer.
Katherine M. Tucker,
Aung Ko Win,
Swati G. Patel,
2021,
The Lancet. Oncology.
Aung Ko Win,
P. Møller,
E. Hovig,
2019,
Genetics in Medicine.
A. Huber,
K. Heinimann,
P. Miny,
2010,
American journal of medical genetics. Part A.
S. Gallati,
A. Schaller,
Thomas von Kanel,
2010,
Clinical chemistry.
P. Chappuis,
P. Hutter,
R. Scott,
1999,
Cancer research.
A. Huber,
J. Sidler,
G. Ramelli,
2012,
Clinical dysmorphology.
M. Zavolan,
S. Kishore,
L. Terracciano,
2014,
Cancer research.
C. Albrecht,
K. Heinimann,
P. Bauerfeind,
2002,
Anticancer research.
R. Chaoui,
J. Hench,
S. Hoeller,
2019,
European Journal of Human Genetics.
L. Terracciano,
C. Quintavalle,
D. Baumhoer,
2019,
Scientific Reports.
G. Marra,
K. Heinimann,
M. Buser,
2012,
Genes, chromosomes & cancer.
D. Kerr,
E. Papaemmanuil,
J. Peto,
2008,
Nature Genetics.
S. Ollila,
M. Nyström,
M. Kansikas,
2010,
British Journal of Cancer.
M. Kloor,
P. Møller,
E. Hovig,
2019,
Hereditary Cancer in Clinical Practice.
S. Gallati,
P. Itin,
P. Lapunzina,
2016,
Molecular genetics & genomic medicine.
A. Zettl,
K. Heinimann,
D. Koeberle,
2016,
Swiss medical weekly.
S. Ollila,
G. Marra,
K. Heinimann,
2006,
Cancer research.
M. Zavolan,
S. Kishore,
L. Terracciano,
2013
.
K. Heinimann,
M. Kovác,
B. Reichlin,
2011,
Journal of Medical Genetics.
K. Heinimann,
W. Weber,
H. Müller,
1997,
International journal of cancer.
Aung Ko Win,
M. von Knebel Doeberitz,
B. Bonanni,
2023,
EClinicalMedicine.
R. Ashfaq,
L. Terracciano,
S. Gokaslan,
2015,
Genes, Chromosomes and Cancer.
M. Southey,
W. Bodmer,
A. Rowan,
2003,
American journal of human genetics.
A. Peyer,
D. Fischer,
K. Heinimann,
2013,
Neuromuscular Disorders.
N. Probst-Hensch,
P. Chappuis,
C. Monnerat,
2022,
Cancers.
B. Zimmermann,
L. Knabben,
D. Shaw,
2020,
European Journal of Human Genetics.
Yoav Goldberg,
A. Wagner,
W. Sjursen,
2017,
Familial Cancer.
A. Spigelman,
N. Lindor,
P. Möller,
2012,
Colorectal disease : the official journal of the Association of Coloproctology of Great Britain and Ireland.
O. Eickelberg,
M. Bihl,
M. Tamm,
2002,
American journal of respiratory cell and molecular biology.
Prevalence of skin lesions in familial adenomatous polyposis: a marker for presymptomatic diagnosis?
P. Itin,
K. Heinimann,
B. Burger,
2011,
The oncologist.
P. Itin,
K. Heinimann,
B. Burger,
2010,
European journal of dermatology : EJD.
M. Kloor,
P. Møller,
E. Hovig,
2019
.
K. Heinimann,
H. Müller,
Z. Dobbie,
2000,
The New England journal of medicine.
C. Albrecht,
K. Heinimann,
P. Tondelli,
2002,
Anticancer Research.
A. Campbell,
J. Sampson,
Lynn Martin,
2023,
Nature communications.
S. Lévesque,
G. Szinnai,
K. Heinimann,
2019,
Thyroid : official journal of the American Thyroid Association.
K. Heinimann,
2018,
Therapeutische Umschau. Revue thérapeutique.
R. Chaoui,
J. Hench,
S. Hoeller,
2019,
European Journal of Human Genetics.
Jenny C. Taylor,
S. Leedham,
K. Howarth,
2015
.
K. Heinimann,
P. Miny,
S. Buechner,
2004,
Journal of Medical Genetics.
D. Bartholdi,
S. Hoeller,
T. Kühne,
2015,
European journal of haematology.
P. Devilee,
F. Fostira,
I. Fokkema,
2010,
Human mutation.
P. Chappuis,
F. Ciorba,
M. Katapodi,
2023,
Cancers.
B. Zimmermann,
L. Knabben,
D. Shaw,
2020,
European Journal of Human Genetics.
G. Szinnai,
K. Heinimann,
M. Janner,
2023,
Archives of Pediatrics.
Prevalence of skin lesions in familial adenomatous polyposis: a marker for presymptomatic diagnosis?
P. Itin,
K. Heinimann,
B. Burger,
2011,
The oncologist.
B. Bonanni,
E. Hovig,
S. Nakken,
2023,
Hereditary Cancer in Clinical Practice.
M. Delorenzi,
M. Hegi,
M. Hamou,
2012,
Neuro-oncology.
G. Marra,
K. Heinimann,
P. Peltomaki,
2006,
Cancer research.
K. Heinimann,
Melanie Gass,
Britta Seebauer,
2024,
Molecular genetics & genomic medicine.
S. Farrington,
C. Tops,
A. Laner,
2022
.
M. Zavolan,
L. Terracciano,
P. Peltomäki,
2014,
Cancer research.