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The Size–Life Span Trade-Off Decomposed: Why Large Dogs Die Young

The American naturalist, 2013-04, Vol.181 (4), p.492-505

2013

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Mutations in MEF2C from the 5q14.3q15 microdeletion syndrome region are a frequent cause of severe mental retardation and diminish MECP2 and CDKL5 expression

Human mutation, 2010-06, Vol.31 (6), p.722-733

2010

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The mutational and phenotypic spectrum of TUBA1A-associated tubulinopathy

Orphanet journal of rare diseases, 2019-02, Vol.14 (1), p.38-38, Article 38

2019

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Distractible dogs, constant cats? A test of the distraction hypothesis in two domestic species

Animal behaviour, 2014-07, Vol.93, p.173-181

2014

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Senescence or selective disappearance? Age trajectories of body mass in wild and captive populations of a small-bodied primate

Proceedings of the Royal Society. B, Biological sciences, 2014-09, Vol.281 (1791), p.20140830-20140830

2014

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Genetic screening confirms heterozygous mutations in ACAN as a major cause of idiopathic short stature

Scientific reports, 2017-09, Vol.7 (1), p.12225-6, Article 12225

2017

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Stress-related changes in leukocyte profiles and telomere shortening in the shortest-lived tetrapod, Furcifer labordi

BMC ecology and evolution, 2020-12, Vol.20 (1), p.160, Article 160

2020

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The costs of risky male behaviour: sex differences in seasonal survival in a small sexually monomorphic primate

Proceedings of the Royal Society. B, Biological sciences, 2008-07, Vol.275 (1643), p.1635-1644

2008

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A novel splice variant expands the LAMC3‐associated cortical phenotype to frontal only polymicrogyria and adult‐onset epilepsy

American journal of medical genetics. Part A, 2020-11, Vol.182 (11), p.2761-2764

2020

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Stable DNA Methylation Boundaries and Expanded Trinucleotide Repeats: Role of DNA Insertions

Journal of molecular biology, 2014-07, Vol.426 (14), p.2554-2566

2014

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Addition of triple negativity of breast cancer as an indicator for germline mutations in predisposing genes increases sensitivity of clinical selection criteria

BMC cancer, 2018-09, Vol.18 (1), p.926-926, Article 926

2018

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A biallelic truncating AEBP1 variant causes connective tissue disorder in two siblings

American journal of medical genetics. Part A, 2019-01, Vol.179 (1), p.50-56

2019

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Influence of reproductive season and rank on fecal glucocorticoid levels in free-ranging male Verreaux's sifakas ( Propithecus verreauxi)

Hormones and behavior, 2007-05, Vol.51 (5), p.640-648

2007

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Dissecting TSC2-mutated renal and hepatic angiomyolipomas in an individual with ARID1B-associated intellectual disability

BMC cancer, 2019-05, Vol.19 (1), p.435-435, Article 435

2019

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Parasite burden in a short-lived chameleon, Furcifer labordi

International journal for parasitology. Parasites and wildlife, 2019-12, Vol.10, p.231-240

2019

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Breast MRI texture analysis for prediction of BRCA-associated genetic risk

BMC medical imaging, 2020-07, Vol.20 (1), p.1-86, Article 86

2020

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Ist der Gruppe noch zu helfen? Gruppendynamik und Individualisierung

1, 2006

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Mutation in the Scyl1 gene encoding amino-terminal kinase-like protein causes a recessive form of spinocerebellar neurodegeneration

EMBO reports, 2007-07, Vol.8 (7), p.691-697

2007

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Highly variable cutis laxa resulting from a dominant splicing mutation of the elastin gene

American journal of medical genetics. Part A, 2008-04, Vol.146A (8), p.977-983

2008

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Highly variable lifespan in an annual reptile, Labord's chameleon (Furcifer labordi)

Scientific reports, 2017-09, Vol.7 (1), p.11397-5, Article 11397

2017

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A Dual Phenotype of Periventricular Nodular Heterotopia and Frontometaphyseal Dysplasia in One Patient Caused by a Single FLNA Mutation Leading to Two Functionally Different Aberrant Transcripts

American journal of human genetics, 2004-04, Vol.74 (4), p.731-737

2004

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stress of growing old: sex- and season-specific effects of age on allostatic load in wild grey mouse lemurs

Oecologia, 2015-08, Vol.178 (4), p.1063-1075

2015

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Exome Pool-Seq in neurodevelopmental disorders

European journal of human genetics : EJHG, 2017-12, Vol.25 (12), p.1364-1376

2017

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Complete basal cell carcinoma remission with imiquimod in a patient with nevoid basal cell carcinoma syndrome and associated basal cell carcinoma of the scalp and invasive ductal breast cancer

Journal of the American Academy of Dermatology, 2011-03, Vol.64 (3), p.611-613

2011

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Severe manifestation of Rauch‐Azzarello syndrome associated with biallelic deletion of CTNND2

Clinical genetics, 2024-08, Vol.106 (2), p.180-186

2024

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The Size–Life Span Trade-Off Decomposed: Why Large Dogs Die Young

Mutations in MEF2C from the 5q14.3q15 microdeletion syndrome region are a frequent cause of severe mental retardation and diminish MECP2 and CDKL5 expression

The mutational and phenotypic spectrum of TUBA1A-associated tubulinopathy

Distractible dogs, constant cats? A test of the distraction hypothesis in two domestic species

Senescence or selective disappearance? Age trajectories of body mass in wild and captive populations of a small-bodied primate

Genetic screening confirms heterozygous mutations in ACAN as a major cause of idiopathic short stature

Stress-related changes in leukocyte profiles and telomere shortening in the shortest-lived tetrapod, Furcifer labordi

The costs of risky male behaviour: sex differences in seasonal survival in a small sexually monomorphic primate

A novel splice variant expands the LAMC3‐associated cortical phenotype to frontal only polymicrogyria and adult‐onset epilepsy

Stable DNA Methylation Boundaries and Expanded Trinucleotide Repeats: Role of DNA Insertions

Addition of triple negativity of breast cancer as an indicator for germline mutations in predisposing genes increases sensitivity of clinical selection criteria

A biallelic truncating AEBP1 variant causes connective tissue disorder in two siblings

Influence of reproductive season and rank on fecal glucocorticoid levels in free-ranging male Verreaux's sifakas ( Propithecus verreauxi)

Dissecting TSC2-mutated renal and hepatic angiomyolipomas in an individual with ARID1B-associated intellectual disability

Parasite burden in a short-lived chameleon, Furcifer labordi

Breast MRI texture analysis for prediction of BRCA-associated genetic risk

Ist der Gruppe noch zu helfen? Gruppendynamik und Individualisierung

Mutation in the Scyl1 gene encoding amino-terminal kinase-like protein causes a recessive form of spinocerebellar neurodegeneration

Highly variable cutis laxa resulting from a dominant splicing mutation of the elastin gene

Highly variable lifespan in an annual reptile, Labord's chameleon (Furcifer labordi)

A Dual Phenotype of Periventricular Nodular Heterotopia and Frontometaphyseal Dysplasia in One Patient Caused by a Single FLNA Mutation Leading to Two Functionally Different Aberrant Transcripts

stress of growing old: sex- and season-specific effects of age on allostatic load in wild grey mouse lemurs

Exome Pool-Seq in neurodevelopmental disorders

Complete basal cell carcinoma remission with imiquimod in a patient with nevoid basal cell carcinoma syndrome and associated basal cell carcinoma of the scalp and invasive ductal breast cancer

Severe manifestation of Rauch‐Azzarello syndrome associated with biallelic deletion of CTNND2

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