K. Oexle
发表
H. Stefánsson,
K. Stefánsson,
T. Gislason,
2017,
Nature Genetics.
Rémy Bruggmann,
Gabor Matyas,
Janine Meienberg,
2016,
Human Genetics.
Yara T. E. Lechanteur,
Christine Binquet,
Elena Prokofyeva,
2017,
Ophthalmology.
A. Kaindl,
K. Oexle,
2009
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T. Meitinger,
M. Hempel,
K. Oexle,
2013,
American journal of medical genetics. Part A.
Milly S. Tedja,
David M. Evans,
C. Sudlow,
2020,
Communications Biology.
S. Burdach,
M. Hempel,
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2012,
Journal of pediatric endocrinology & metabolism : JPEM.
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Clinical genetics.
K. Fliessbach,
H. Obrig,
A. Winkler,
2021,
Molecular Psychiatry.
B. Koletzko,
R. Obeid,
K. Oexle,
2016,
Journal of perinatal medicine.
Milly S. Tedja,
Claire L. Simpson,
David M. Evans,
2016,
Nature Communications.
C. Gieger,
A. Hofman,
A. Uitterlinden,
2014,
PloS one.
Claire L. Simpson,
A. Hofman,
A. Uitterlinden,
2012,
Human Genetics.
Thomas Meitinger,
Toomas Haller,
Andres Metspalu,
2013,
American journal of human genetics.
J. Connor,
R. Allen,
K. Oexle,
2017,
Sleep medicine.
K. Oexle,
A. Zwirner,
1997,
Human molecular genetics.
J. Enghild,
S. Thiel,
A. Hansen,
2017,
The Journal of Immunology.
J. Enghild,
S. Thiel,
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2017
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C. Gieger,
A. Peters,
T. Wieland,
2014,
Movement disorders : official journal of the Movement Disorder Society.
Juliane,
Winkelmann,
C. Gieger,
2020
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K. Oexle,
A. Kohlschütter,
A. Speer,
1997,
Pediatric Research.
Milly S. Tedja,
Srujana,
T. Lehtimäki,
2019
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J. Winkelmann,
A. Ludolph,
E. Graf,
2022,
Neurobiology of Aging.
Christian Gieger,
Thomas Meitinger,
Andres Metspalu,
2015,
Nature Communications.
D. Horn,
H. Kehrer-Sawatzki,
E. Seemanová,
2005,
European Journal of Human Genetics.
C. van Broeckhoven,
B. Rautenstrauss,
V. Timmerman,
2000,
Journal of Neurology.
C. Hübner,
T. Voit,
K. Oexle,
1998
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J. Winkelmann,
A. Salminen,
B. Schormair,
2020,
Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine.
C. Gieger,
R. Treede,
A. Pfeufer,
2011,
BMC neurology.
T. Meitinger,
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K. Bidzhekov,
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Diabetes Care.
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R. Krüger,
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T. Roscioli,
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Journal of Medical Genetics.
C. Hübner,
T. Voit,
K. Oexle,
1996,
Human molecular genetics.
K. Oexle,
2006,
Journal of Human Genetics.
K. Oexle,
A. Kohlschütter,
A. Kohlschütter,
2001,
Neuropediatrics.
A. Vortmeyer,
O. Dammann,
K. Oexle,
1992,
European Journal of Pediatrics.
Claire L. Simpson,
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C. Gieger,
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Human Genetics.
A. Uitterlinden,
T. Spector,
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Cell.
C. Gieger,
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PloS one.
K. Oexle,
Konrad Oexle,
1998,
Journal of theoretical biology.
K. Oexle,
2010,
Journal of Human Genetics.
T. Meitinger,
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EBioMedicine.
Gabriëlle H S Buitendijk,
Claire L. Simpson,
David M. Evans,
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Nature Genetics.
H. Goebel,
C. Hübner,
K. Oexle,
1997,
Neuromuscular Disorders.
H. Grundmann,
H. Blum,
W. Offensperger,
1989,
Zentralblatt fur Bakteriologie, Mikrobiologie, und Hygiene. Series A, Medical microbiology, infectious diseases, virology, parasitology.
K. Pelin,
F. Muntoni,
R. Sutphen,
1999,
Nature Genetics.
A. Jauch,
T. Meitinger,
T. Strom,
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European journal of medical genetics.
J. Weis,
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Human mutation.
J. Winkelmann,
Nazanin Mirza-Schreiber,
W. Krężel,
2021,
bioRxiv.
K. Oexle,
2006,
European Journal of Pediatrics.
J. Winkelmann,
K. Oexle,
2018,
Neuron.
Tentative clinical diagnosis of Lujan‐Fryns syndrome—A conglomeration of different genetic entities?
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European Journal of Pediatrics.
Gabriëlle H S Buitendijk,
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A. Hofman,
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Nature Genetics.
A. Rump,
C. Fauth,
S. Tinschert,
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American journal of medical genetics. Part A.
K. Oexle,
G. Mátyás,
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American journal of medical genetics. Part A.
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Toshiko Tanaka,
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Annals of neurology.
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Nature Communications.
C. Gieger,
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T. Meitinger,
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European Journal of Human Genetics.
Claire L. Simpson,
David M. Evans,
C. Gieger,
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Scientific Reports.
Christian Gieger,
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Paul Mitchell,
2013,
Human molecular genetics.
Stephen H. Bell,
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C. Gieger,
2022
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K. Oexle,
2021,
Strategies for Sustainability of the Earth System.
K. Oexle,
2016,
Journal of Human Genetics.
H. Blum,
K. Oexle,
Konrad Oexle,
2014
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F. Kronenberg,
W. Rathmann,
A. Peters,
2015,
European journal of endocrinology.
S. Tinschert,
K. Oexle,
M. Lee-Kirsch,
2008,
Journal of Inherited Metabolic Disease.
K. Oexle,
2018,
Sleep.
M. Schliwa,
K. Oexle,
1989,
Biology of the cell.
K. Campbell,
F. Leturcq,
J. Kaplan,
1996,
Neuropediatrics.
K. Oexle,
R. Heyer,
1999,
Annals of neurology.
R. Jech,
S. Schneider,
B. Haslinger,
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Movement disorders : official journal of the Movement Disorder Society.
T. Mayer,
S. Tinschert,
K. Oexle,
2005,
European Journal of Pediatrics.
Adriana I. Iglesias,
T. Lehtimäki,
J. Jonas,
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Communications Biology.
Gabriëlle H S Buitendijk,
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European Journal of Epidemiology.
W. Chung,
J. Volkmann,
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The Lancet Neurology.
B. Hemmer,
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2011
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B. Meyer,
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Acta Neurochirurgica.
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Human Genetics.
C. Gieger,
M. Waldenberger,
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Brain : a journal of neurology.
C. Gieger,
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Journal of Medical Genetics.
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Matthias W. Riepe,
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M. Riepe,
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Brain Research.
B. Hemmer,
J. Winkelmann,
K. Oexle,
2011,
Movement disorders : official journal of the Movement Disorder Society.
H. Prokisch,
J. Winkelmann,
V. Mall,
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Annals of neurology.
Jonathan H. Morgan,
Adriana I. Iglesias,
Kristina L. H. Lee,
2023,
EBioMedicine.
M. Nöthen,
M. Müller-Nurasyid,
B. Müller-Myhsok,
2022,
Sleep medicine.
Christian Gieger,
Thomas Meitinger,
Karsten Suhre,
2012,
Genetic epidemiology.
K. Oexle,
1989,
New England Journal of Medicine.
R. Jech,
B. Haslinger,
J. Winkelmann,
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European Journal of Human Genetics.
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medRxiv.
Jonathan H. Morgan,
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Nature Genetics.
Jonathan H. Morgan,
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JAMA ophthalmology.
Jonathan H. Morgan,
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PloS one.
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A. Auton,
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The Lancet Neurology.
C. Gieger,
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Movement disorders : official journal of the Movement Disorder Society.
Benjamin J. Wright,
C. Gieger,
J. Pankow,
2011
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L. Bonafė,
K. Oexle,
B. Steinmann,
2002,
Molecular genetics and metabolism.
T. Meitinger,
M. Hempel,
K. Oexle,
2013,
American journal of medical genetics. Part A.
K. Oexle,
G. Mátyás,
P. Naef,
2014,
American journal of medical genetics. Part A.
Adriana I. Iglesias,
Claire L. Simpson,
T. Lehtimäki,
2023,
Communications Biology.
A. Rump,
C. Fauth,
S. Tinschert,
2013,
American journal of medical genetics. Part A.
C. Gieger,
B. Schormair,
K. Oexle,
2024,
EBioMedicine.