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Local seed dispersal in European silver fir (Abies alba Mill.): lessons learned from a seed trap experiment

Trees (Berlin, West), 2012-06, Vol.26 (3), p.987-996

2012

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Population genetics of silver fir (abies alba mill.) in the northern black forest

Cremer, Eva

2009

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Six newly developed microsatellite markers of Laccaria amethystina, using an improved CSSR approach

Mycological progress, 2008-11, Vol.7 (4), p.285-290

2008

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Calcium Directly Regulates Phosphatidylinositol 4,5-Bisphosphate Headgroup Conformation and Recognition

Journal of the American Chemical Society, 2017-03, Vol.139 (11), p.4019-4024

2017

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Clonal haematopoiesis in chronic ischaemic heart failure: prognostic role of clone size for DNMT3A- and TET2-driver gene mutations

European heart journal, 2021-01, Vol.42 (3), p.257-265

2021

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Thyroid-Hormone-Induced Browning of White Adipose Tissue Does Not Contribute to Thermogenesis and Glucose Consumption

Cell reports (Cambridge), 2019-06, Vol.27 (11), p.3385-3400.e3

2019

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Prinzessinnen unterwegs: Reisen fürstlicher Frauen in der Frühen Neuzeit

1st edition., 2017

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Revesz syndrome revisited

Orphanet journal of rare diseases, 2020-10, Vol.15 (1), p.1-299, Article 299

2020

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Frequent horizontal chromosome transfer between asexual fungal insect pathogens

Proceedings of the National Academy of Sciences - PNAS, 2024-03, Vol.121 (11), p.e2316284121

2024

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Determining the Effects of Training Duration on the Behavioral Expression of Habitual Control in Humans: A Multilaboratory Investigation

Learning & memory (Cold Spring Harbor, N.Y.), 2022-01, Vol.29 (1), p.16-28

2022

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Five-year outcome in 18 010 patients from the German Aortic Valve Registry

European journal of cardio-thoracic surgery, 2021-11, Vol.60 (5), p.1139-1146

2021

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Loss-of-function variants of SETD5 cause intellectual disability and the core phenotype of microdeletion 3p25.3 syndrome

European journal of human genetics : EJHG, 2015-06, Vol.23 (6), p.753-760

2015

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Studies on the association of malondialdehyde as a biomarker for oxidative stress and degree of malignancy in dogs with mammary adenocarcinomas

Veterinary medicine and science, 2024-07, Vol.10 (4), p.e1496-n/a

2024

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Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study

The Lancet (British edition), 2012-11, Vol.380 (9854), p.1674-1682

2012

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Regional importation and asymmetric within-country spread of SARS-CoV-2 variants of concern in the Netherlands

eLife, 2022-09, Vol.11

2022

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Outcome of Stable Patients With Acute Myocardial Infarction and Coronary Artery Bypass Surgery Within 48 Hours: A Single‐Center, Retrospective Experience

Journal of the American Heart Association, 2017-10, Vol.6 (10), p.n/a

2017

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Biodiverse edible schools: Linking healthy food, school gardens and local urban biodiversity

Urban forestry & urban greening, 2019-04, Vol.40, p.35-43

2019

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How representative are neuroimaging samples? Large-scale evidence for trait anxiety differences between fMRI and behaviour-only research participants

Social cognitive and affective neuroscience, 2021-10, Vol.16 (10), p.1057-1070

2021

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The effect of six months of elastic band resistance training, nutritional supplementation or cognitive training on chromosomal damage in institutionalized elderly

Experimental gerontology, 2015-05, Vol.65, p.16-22

2015

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Impact of chronic kidney disease in 29 893 patients undergoing transcatheter or surgical aortic valve replacement from the German Aortic Valve Registry

European journal of cardio-thoracic surgery, 2021-04, Vol.59 (3), p.532-544

2021

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Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications

Scientific reports, 2021-01, Vol.11 (1), p.1526-1526, Article 1526

2021

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Disruption of NEUROD2 causes a neurodevelopmental syndrome with autistic features via cell-autonomous defects in forebrain glutamatergic neurons

Molecular psychiatry, 2021-11, Vol.26 (11), p.6125-6148

2021

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De Novo Mutations in CHAMP1 Cause Intellectual Disability with Severe Speech Impairment

American journal of human genetics, 2015-09, Vol.97 (3), p.493-500

2015

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Nine newly identified individuals refine the phenotype associated with MYT1L mutations

American journal of medical genetics. Part A, 2020-05, Vol.182 (5), p.1021-1031

2020

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Local seed dispersal in European silver fir (Abies alba Mill.): lessons learned from a seed trap experiment

Population genetics of silver fir (abies alba mill.) in the northern black forest

Six newly developed microsatellite markers of Laccaria amethystina, using an improved CSSR approach

Calcium Directly Regulates Phosphatidylinositol 4,5-Bisphosphate Headgroup Conformation and Recognition

Clonal haematopoiesis in chronic ischaemic heart failure: prognostic role of clone size for DNMT3A- and TET2-driver gene mutations

Thyroid-Hormone-Induced Browning of White Adipose Tissue Does Not Contribute to Thermogenesis and Glucose Consumption

Prinzessinnen unterwegs: Reisen fürstlicher Frauen in der Frühen Neuzeit

Revesz syndrome revisited

Frequent horizontal chromosome transfer between asexual fungal insect pathogens

SAMHD1 is a biomarker for cytarabine response and a therapeutic target in acute myeloid leukemia

Determining the Effects of Training Duration on the Behavioral Expression of Habitual Control in Humans: A Multilaboratory Investigation

Five-year outcome in 18 010 patients from the German Aortic Valve Registry

Loss-of-function variants of SETD5 cause intellectual disability and the core phenotype of microdeletion 3p25.3 syndrome

Studies on the association of malondialdehyde as a biomarker for oxidative stress and degree of malignancy in dogs with mammary adenocarcinomas

Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study

Regional importation and asymmetric within-country spread of SARS-CoV-2 variants of concern in the Netherlands

Outcome of Stable Patients With Acute Myocardial Infarction and Coronary Artery Bypass Surgery Within 48 Hours: A Single‐Center, Retrospective Experience

Biodiverse edible schools: Linking healthy food, school gardens and local urban biodiversity

How representative are neuroimaging samples? Large-scale evidence for trait anxiety differences between fMRI and behaviour-only research participants

The effect of six months of elastic band resistance training, nutritional supplementation or cognitive training on chromosomal damage in institutionalized elderly

Impact of chronic kidney disease in 29 893 patients undergoing transcatheter or surgical aortic valve replacement from the German Aortic Valve Registry

Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications

Disruption of NEUROD2 causes a neurodevelopmental syndrome with autistic features via cell-autonomous defects in forebrain glutamatergic neurons

De Novo Mutations in CHAMP1 Cause Intellectual Disability with Severe Speech Impairment

Nine newly identified individuals refine the phenotype associated with MYT1L mutations

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