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Martin Kehrer
Observed names:
Kehrer, Martin,
M Kehrer,
M. Kehrer,
M. Kehrer,
Μ. Kehrer
Institutions:
Universitätsklinikum Tübingen,
University of Tübingen
Observed institutions:
Universitätsklinikum Tübingen,
University Children's Hospital Tübingen,
Hertie Institute for Clinical Brain Research,
University of Tübingen
ORCID:
0000-0002-0324-6925
Observed ORCID:
0000-0002-0324-6925
OpenAlex ID:
A5066348261
Next-generation sequencing in X-linked intellectual disability
2015
·
Andreas Tzschach
, Ute Grasshoff
, et al.
·
European Journal of Human Genetics
·
147
Development of Cerebral Blood Flow Volume in Preterm Neonates during the First Two Weeks of Life
2005
·
Martin Kehrer
, Gunnar Blumenstock
, et al.
·
Pediatric Research
·
96
Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings
2024
·
Axel Schmidt
, Magdalena Danyel
, et al.
·
Nature Genetics
·
59
The Development of Cerebral Perfusion in Healthy Preterm and Term Neonates
2003
·
M. Kehrer
, I. Krägeloh-Mann
, et al.
·
Neuropediatrics
·
50
Measurement of volume of cerebral blood flow in healthy preterm and term neonates with ultrasound
2002
·
M Kehrer
, R Goelz
, et al.
·
The Lancet
·
50
Incidence of IDDM in German Children Aged 0–14 years: A 6-year population-based study (1987–1993)
1997
·
Andreas Neu
, Martin Kehrer
, et al.
·
Diabetes Care
·
49
HBOC multi-gene panel testing: comparison of two sequencing centers
2015
·
Christopher Schroeder
, Ulrike Faust
, et al.
·
Breast Cancer Research and Treatment
·
47
Varying clinical presentations at onset of type 1 diabetes mellitus in children - epidemiological evidence for different subtypes of the disease?
2001
·
Andreas Neu
, Stefan Ehehalt
, et al.
·
Pediatric Diabetes
·
46
PDF
Bi-allelic loss-of-function variants in KIF21A cause severe fetal akinesia with arthrogryposis multiplex
2021
·
Ruth J Falb
, Amelie J Müller
, et al.
·
Journal of Medical Genetics
·
45
PDF
Diabetes incidence in children of different nationalities: an epidemiological approach to the pathogenesis of diabetes
2001
·
A. Neu
, A. Willasch
, et al.
·
Diabetologia
·
40
PDF
Postnatal decrease in substantia nigra echogenicity
2004
·
Alexander Iova
, Andrew Garmashov
, et al.
·
Journal of Neurology
·
37
Rising Incidence of Type 1 Diabetes in Germany
2001
·
Andreas Neu
, Stefan Ehehalt
, et al.
·
Diabetes Care
·
36
PDF
A Longitudinal Study of Cerebral Blood Flow Over the First 30 Months
2009
·
Martin Kehrer
, Martin Schöning
·
Pediatric Research
·
30
Investigating the effects of additional truncating variants in DNA-repair genes on breast cancer risk in BRCA1-positive women
2019
·
Ilnaz Sepahi
, Ulrike Faust
, et al.
·
BMC Cancer
·
24
PDF
Floating‐Harbor syndrome: SRCAP mutations are not restricted to exon 34
2013
·
M. Kehrer
, A. Beckmann
, et al.
·
Clinical Genetics
·
23
Cerebral blood flow volume measurements with ultrasound: Interobserver reproducibility in preterm and term neonates
2005
·
Stefan Ehehalt
, Martin Kehrer
, et al.
·
Ultrasound in Medicine & Biology
·
20
Seasonality of Birth in Children (0-14 Years) with Diabetes Mellitus Type 1 in Baden-Wuerttemberg, Germany
2000
·
A. Neu
, Μ. Kehrer
, et al.
·
Journal of Pediatric Endocrinology and Metabolism
·
19
The development of haemodynamics in the extracranial cerebral arteries of healthy preterm and term neonates
2004
·
Martin Kehrer
, Rangmar Goelz
, et al.
·
Ultrasound in Medicine & Biology
·
14
Next-generation phenotyping integrated in a national framework for patients with ultra-rare disorders improves genetic diagnostics and yields new molecular findings
2023
·
Axel Schmidt
, Magdalena Danyel
, et al.
·
medRxiv
·
12
PDF
A single center experience of prenatal parent‐fetus trio exome sequencing for pregnancies with congenital anomalies
2022
·
Andreas Dufke
, Markus Hoopmann
, et al.
·
Prenatal Diagnosis
·
11
PDF
Novel HIVEP2 Variants in Patients with Intellectual Disability
2019
·
Joohyun Park
, Roberto Colombo
, et al.
·
Molecular Syndromology
·
10
Interstitial 1p32.1p32.3 deletion in a patient with multiple congenital anomalies
2015
·
Martin Kehrer
, Karin Schäferhoff
, et al.
·
American Journal of Medical Genetics Part A
·
8
Diabeteshäufigkeit bei Kindern und Jugendlichen in Deutschland – 20 Jahre Diabetes-Inzidenzregister Baden-Württemberg
2008
·
A. Neu
, S. Ehehalt
, et al.
·
Diabetologie und Stoffwechsel
·
8
Interstitial duplication of chromosome region 1q25.1q25.3: Report of a patient with mild cognitive deficits, tall stature and facial dysmorphisms
2015
·
Martin Kehrer
, Thomas Liehr
, et al.
·
American Journal of Medical Genetics Part A
·
6
The Effect of Vasospasm on Cerebral Perfusion: A Colour Duplex Study of the Extra- and Intracranial Cerebral Arteries
2012
·
Martin Schöning
, Peter Scheel
, et al.
·
Ultrasound in Medicine & Biology
·
6
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Works count:
55
Citation count:
920
H-index:
17
I10-index:
21
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