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Co-authors
(228)
Michael Z. Ludwig
21
Friedhelm Hildebrandt
8
Massimo Attanasio
7
Edgar A. Otto
7
Heiko Reutter
6
Journals
(25)
EXP CLIN ENDOCRINOL DIABETES
2
AMER J KIDNEY DIS
2
J MED GENET
2
J PEDIAT
2
KIDNEY BLOOD PRESSURE RES
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Academic
Authors
Boris Utsch
Boris Utsch,Universitatsspital Bern,Genetics & Genealogy,Urology,Family Medicine
Edit
Boris Utsch
Universitatsspital Bern
Publications:
36
|
Citations:
577
Fields:
Genetics & Genealogy
,
Urology
,
Family Medicine
View FAQ about top research areas and Fields of study
Collaborated with
228 co-authors
from 1998 to 2011
|
Cited by
1940 authors
Cumulative
Annual
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Publications
(36)
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RefWorks
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A Hospital-Based Intermittent Nocturnal Hemodialysis Program for Children and Adolescents
(
Citations: 3
)
Anne Hoppe
,
Christina von Puttkamer
,
Ursula Linke
,
Cindy Kahler
,
Martina Booß
,
Renate Braunauer-Kolberg
,
Katja Hofmann
,
Petra Joachimsky
,
Ingrid Hirte
,
Sylke Schley
,
Boris Utsch
,
Julia Thumfart
http://academic.research.microsoft.com/io.ashx?type=5&id=30896230&selfId1=23520788&selfId2=0&maxNumber=12&query=
Journal:
Journal of Pediatrics - J PEDIAT
, vol. 158, no. 1, pp. 64-68.e1, 2011
Phenotype Severity in the Bladder Exstrophy-Epispadias Complex: Analysis of Genetic and Nongenetic Contributing Factors in 441 Families from North America and Europe
Heiko Reutter
,
Simeon A. Boyadjiev
,
Lisa Gambhir
,
Anne-Karoline Ebert
,
Wolfgang H. Rösch
,
Raimund Stein
,
Annette Schröder
,
Thomas M. Boemers
,
Enrika Bartels
,
Hannes Vogt
,
Boris Utsch
,
Martin Müller
http://academic.research.microsoft.com/io.ashx?type=5&id=49094038&selfId1=23520788&selfId2=0&maxNumber=12&query=
Journal:
Journal of Pediatrics - J PEDIAT
, vol. 159, no. 5, pp. 825-831.e1, 2011
Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11)
(
Citations: 16
)
E. A Otto
,
K. Tory
,
M. Attanasio
,
W. Zhou
,
M. Chaki
,
Y. Paruchuri
,
E. L Wise
,
M T F Wolf
,
B Utsch
,
C. Becker
,
G. Nurnberg
,
P. Nurnberg
http://academic.research.microsoft.com/io.ashx?type=5&id=30638927&selfId1=23520788&selfId2=0&maxNumber=12&query=
Journal:
Journal of Medical Genetics - J MED GENET
, vol. 46, no. 10, pp. 663-670, 2009
Infantile Hypophosphatasia due to a New Compound Heterozygous TNSALP Mutation – Functional Evidence for a Hydrophobic Side-Chain?
(
Citations: 1
)
B. Utsch
,
I. Brun-Heath
,
G. Staatz
,
C. Gravou-Apostolatou
,
S. Karle
,
U. Jacobs
,
M. Ludwig
,
M. Zenker
,
H.-G. Dörr
,
W. Rascher
,
E. Mornet
,
J. Dötsch
Journal:
Experimental and Clinical Endocrinology & Diabetes - EXP CLIN ENDOCRINOL DIABETES
, vol. 117, no. 01, pp. 28-33, 2009
Valsartan fetopathy: a case report
B Huber
,
C Schindera
,
B Utsch
,
M Nelle
,
R Gerull
Journal:
Zeitschrift Fur Geburtshilfe Und Neonatologie - Z GEBURTSH NEONATOLOGIE
, vol. 213, no. S 01, 2009
Sort by:
Citations
(577 times by 383 publications)
Nephronophthisis
(
Citations: 5
)
Matthias T. F. Wolf
,
Friedhelm Hildebrandt
Journal:
Pediatric Nephrology - PEDIAT NEPHROL
, vol. 26, no. 2, pp. 181-194, 2011
Cystic diseases of the kidney: ciliary dysfunction and cystogenic mechanisms
(
Citations: 4
)
Cecilia Gascue
,
Nicholas Katsanis
,
Jose L. Badano
Journal:
Pediatric Nephrology - PEDIAT NEPHROL
, vol. 26, no. 8, pp. 1181-1195, 2011
TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum
(
Citations: 1
)
Erica E Davis
,
Qi Zhang
,
Qin Liu
,
Bill H Diplas
,
Lisa M Davey
,
Jane Hartley
,
Corinne Stoetzel
,
Katarzyna Szymanska
,
Gokul Ramaswami
,
Clare V Logan
,
Donna M Muzny
,
Alice C Young
http://academic.research.microsoft.com/io.ashx?type=5&id=56593681&selfId1=23520788&selfId2=0&maxNumber=12&query=
Journal:
Nature Genetics - NAT GENET
, vol. 43, no. 3, pp. 189-196, 2011
Ciliopathies: an expanding disease spectrum
(
Citations: 2
)
Aoife M. Waters
,
Philip L. Beales
Journal:
Pediatric Nephrology - PEDIAT NEPHROL
, vol. 26, no. 7, pp. 1039-1056, 2011
Complex interactions between genes controlling trafficking in primary cilia
(
Citations: 2
)
Polloneal Jymmiel R Ocbina
,
Jonathan T Eggenschwiler
,
Ivan Moskowitz
,
Kathryn V Anderson
Journal:
Nature Genetics - NAT GENET
, vol. 43, no. 6, pp. 547-553, 2011
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