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Low Physical Activity Accentuates the Effect of the FTO rs9939609 Polymorphism on Body Fat Accumulation

Diabetes (New York, N.Y.), 2008-01, Vol.57 (1), p.95-101

2008

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Frontal alpha oscillations distinguish leaders from followers: Multivariate decoding of mutually interacting brains

NeuroImage (Orlando, Fla.), 2014-07, Vol.94, p.79-88

2014

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Association Between Urinary Markers of Nucleic Acid Oxidation and Mortality in Type 2 Diabetes: A population-based cohort study

Diabetes care, 2013-03, Vol.36 (3), p.669-676

2013

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Clinical benefit of a gluten-free diet in type 1 diabetic children with screening-detected celiac disease : A population-based screening study with 2 years' follow-up

Diabetes care, 2006-11, Vol.29 (11), p.2452-2456

2006

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Identification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment

American journal of medical genetics. Part A, 2011-06, Vol.155A (6), p.1298-1313

2011

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Association of IL-1ra and Adiponectin With C-Peptide and Remission in Patients With Type 1 Diabetes

Diabetes (New York, N.Y.), 2008-04, Vol.57 (4), p.929-937

2008

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Infantile spasms and pigmentary mosaicism

Epilepsia (Copenhagen), 2010-07, Vol.51 (7), p.1317-1318

2010

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The Angiotensin-converting Enzyme Inhibition Post Revascularization Study (APRES)

Journal of the American College of Cardiology, 2000-03, Vol.35 (4), p.881-888

2000

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Mutation analysis of the WFS1 gene in seven Danish Wolfram syndrome families; four new mutations identified

European journal of human genetics : EJHG, 2005-12, Vol.13 (12), p.1275-1284

2005

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Variants Within the Calpain-10 Gene on Chromosome 2q37 (NIDDM1) and Relationships to Type 2 Diabetes, Insulin Resistance, and Impaired Acute Insulin Secretion Among Scandinavian Caucasians

Diabetes (New York, N.Y.), 2002-12, Vol.51 (12), p.3561-3567

2002

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Patients Newly Diagnosed with Clinical Type 2 Diabetes during Oral Glucocorticoid Treatment and Observed for 14 Years: All‐Cause Mortality and Clinical Developments

Basic & clinical pharmacology & toxicology, 2011-04, Vol.108 (4), p.285-288

2011

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Autozygosity mapping of a large consanguineous Pakistani family reveals a novel non-syndromic autosomal recessive mental retardation locus on 11p15-tel

Neurogenetics, 2011-08, Vol.12 (3), p.247-251

2011

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Psychosocial work environment and registered absence from work: Estimating the etiologic fraction

American journal of industrial medicine, 2006-03, Vol.49 (3), p.187-196

2006

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Efficacy and safety of 5-grass-pollen sublingual immunotherapy tablets in pediatric allergic rhinoconjunctivitis

Journal of allergy and clinical immunology, 2009, Vol.123 (1), p.160-166.e3

2009

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Reference interval for serum cystatin C in children

Clinical chemistry (Baltimore, Md.), 1999-10, Vol.45 (10), p.1856-1858

1999

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Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expression

Human genetics, 2008-03, Vol.123 (2), p.177-187

2008

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Beneficial effects of ramipril on left ventricular end-diastolic and end-systolic volume indexes after uncomplicated invasive revascularization are associated with a reduction in cardiac events in patients with moderately impaired left ventricular function and no clinical heart failure

Journal of the American College of Cardiology, 2001-04, Vol.37 (5), p.1214-1220

2001

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Pallister-Killian Syndrome: Multiband FISH of Tetrasomy 12p

Pediatric dermatology, 2006-07, Vol.23 (4), p.378-381

2006

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Genetic Heterogeneity in Microcornea-Cataract: Five Novel Mutations in CRYAA, CRYGD, and GJA8

Investigative ophthalmology & visual science, 2007-09, Vol.48 (9), p.3937-3944

2007

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Comprehensive Mutational Screening in a Cohort of Danish Families with Hereditary Congenital Cataract

Investigative ophthalmology & visual science, 2009-07, Vol.50 (7), p.3291-3303

2009

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Combined Analyses of 20 Common Obesity Susceptibility Variants

Diabetes (New York, N.Y.), 2010-07, Vol.59 (7), p.1667-1673

2010

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Cluster analysis of activity-time series in motor learning

Human brain mapping, 2002-03, Vol.15 (3), p.135-145

2002

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Changes in nasal volume after surgically assisted bone-borne rapid maxillary expansion

American journal of orthodontics and dentofacial orthopedics, 2010-06, Vol.137 (6), p.782-789

2010

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Traumatic bilateral quadriceps tendon rupture

Journal of orthopaedic science : official journal of the Japanese Orthopaedic Association, 2001-04, Vol.6 (2), p.187-188

2001

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Cone Dystrophy with Supernormal Rod Response Is Strictly Associated with Mutations in KCNV2

Investigative ophthalmology & visual science, 2008-02, Vol.49 (2), p.751-757

2008

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Low Physical Activity Accentuates the Effect of the FTO rs9939609 Polymorphism on Body Fat Accumulation

Frontal alpha oscillations distinguish leaders from followers: Multivariate decoding of mutually interacting brains

Association Between Urinary Markers of Nucleic Acid Oxidation and Mortality in Type 2 Diabetes: A population-based cohort study

Clinical benefit of a gluten-free diet in type 1 diabetic children with screening-detected celiac disease : A population-based screening study with 2 years' follow-up

Identification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment

Association of IL-1ra and Adiponectin With C-Peptide and Remission in Patients With Type 1 Diabetes

Infantile spasms and pigmentary mosaicism

The Angiotensin-converting Enzyme Inhibition Post Revascularization Study (APRES)

Mutation analysis of the WFS1 gene in seven Danish Wolfram syndrome families; four new mutations identified

Variants Within the Calpain-10 Gene on Chromosome 2q37 (NIDDM1) and Relationships to Type 2 Diabetes, Insulin Resistance, and Impaired Acute Insulin Secretion Among Scandinavian Caucasians

Patients Newly Diagnosed with Clinical Type 2 Diabetes during Oral Glucocorticoid Treatment and Observed for 14 Years: All‐Cause Mortality and Clinical Developments

Autozygosity mapping of a large consanguineous Pakistani family reveals a novel non-syndromic autosomal recessive mental retardation locus on 11p15-tel

Psychosocial work environment and registered absence from work: Estimating the etiologic fraction

Efficacy and safety of 5-grass-pollen sublingual immunotherapy tablets in pediatric allergic rhinoconjunctivitis

Reference interval for serum cystatin C in children

Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expression

Beneficial effects of ramipril on left ventricular end-diastolic and end-systolic volume indexes after uncomplicated invasive revascularization are associated with a reduction in cardiac events in patients with moderately impaired left ventricular function and no clinical heart failure

Pallister-Killian Syndrome: Multiband FISH of Tetrasomy 12p

Genetic Heterogeneity in Microcornea-Cataract: Five Novel Mutations in CRYAA, CRYGD, and GJA8

Comprehensive Mutational Screening in a Cohort of Danish Families with Hereditary Congenital Cataract

Combined Analyses of 20 Common Obesity Susceptibility Variants

Cluster analysis of activity-time series in motor learning

Changes in nasal volume after surgically assisted bone-borne rapid maxillary expansion

Traumatic bilateral quadriceps tendon rupture

Cone Dystrophy with Supernormal Rod Response Is Strictly Associated with Mutations in KCNV2

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