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ACE: adaptive cluster expansion for maximum entropy graphical model inference

Bioinformatics (Oxford, England), 2016-10, Vol.32 (20), p.3089-3097

2016

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Review of interactive digital solutions improving health literacy of personal cancer risks in the general public

International journal of medical informatics (Shannon, Ireland), 2021-10, Vol.154, p.104564, Article 104564

2021

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Mutations in fibrillin-1 cause congenital scleroderma: stiff skin syndrome

Science translational medicine, 2010-03, Vol.2 (23), p.23ra20

2010

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Zebrafish type I collagen mutants faithfully recapitulate human type I collagenopathies

Proceedings of the National Academy of Sciences - PNAS, 2018-08, Vol.115 (34), p.E8037-E8046

2018

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PO-1052 Cyberknife stereotactic radiotherapy for vestibular schwannomas :a single institution experience

Radiotherapy and oncology, 2021-08, Vol.161, p.S876-S876

2021

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Expert consensus for multi-modality imaging evaluation of cardiovascular complications of radiotherapy in adults: a report from the European Association of Cardiovascular Imaging and the American Society of Echocardiography

European heart journal cardiovascular imaging, 2013-08, Vol.14 (8), p.721-740

2013

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Hearing loss in Waardenburg syndrome: a systematic review

Clinical genetics, 2016-04, Vol.89 (4), p.416-425

2016

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Recurrent Mutation in the First Zinc Finger of the Orphan Nuclear Receptor NR2E3 Causes Autosomal Dominant Retinitis Pigmentosa

American journal of human genetics, 2007-07, Vol.81 (1), p.147-157

2007

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The COVID-19 pandemic : a real opportunity for digital health

Revue médicale de Liège, 2020, Vol.75 (S1), p.74

2020

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Exome sequencing revealed a novel biallelic deletion in the DCAF17 gene underlying Woodhouse Sakati syndrome

Clinical genetics, 2016-09, Vol.90 (3), p.263-269

2016

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Zebrafish Collagen Type I: Molecular and Biochemical Characterization of the Major Structural Protein in Bone and Skin

Scientific reports, 2016-02, Vol.6 (1), p.21540-21540, Article 21540

2016

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Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome

Nature genetics, 2006-04, Vol.38 (4), p.452-457

2006

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A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2

Nature genetics, 2005-03, Vol.37 (3), p.275-281

2005

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Effect of Mutation Type and Location on Clinical Outcome in 1,013 Probands with Marfan Syndrome or Related Phenotypes and FBN1 Mutations: An International Study

American journal of human genetics, 2007-09, Vol.81 (3), p.454-466

2007

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Pharma industry reinvents itself in the turmoil. Part 2. Opportunities

Revue médicale de Liège, 2021-04, Vol.76 (4), p.292

Coucke, P A

2021

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Generation and Validation of a Complete Knockout Model of abcc6a in Zebrafish

Journal of investigative dermatology, 2018-11, Vol.138 (11), p.2333-2342

2018

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TEAD4 regulates trophectoderm differentiation upstream of CDX2 in a GATA3-independent manner in the human preimplantation embryo

Human reproduction (Oxford), 2022-07, Vol.37 (8), p.1760-1773

2022

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Pharma industry reinvents itself in the turmoil. Part 1. Challenges

Revue médicale de Liège, 2021-03, Vol.76 (3), p.216

Coucke, P A

2021

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Mutation detection in the ABCC6 gene and genotype–phenotype analysis in a large international case series affected by pseudoxanthoma elasticum

Journal of medical genetics, 2007-10, Vol.44 (10), p.621-628

2007

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Cumulus cell gene expression predicts better cleavage-stage embryo or blastocyst development and pregnancy for ICSI patients

Human reproduction (Oxford), 2011-05, Vol.26 (5), p.1035-1051

2011

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Risk management and (health) crisis: How to assess the impact of changing a prescription over time in radiotherapy

Cancer radiothérapie, 2021-05, Vol.25 (3), p.268-270

2021

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The Abcc6a Knockout Zebrafish Model as a Novel Tool for Drug Screening for Pseudoxanthoma Elasticum

Frontiers in pharmacology, 2022-03, Vol.13, p.822143-822143

2022

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Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis

Nature genetics, 2004-11, Vol.36 (11), p.1213-1218

2004

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Arterial tortuosity syndrome: clinical and molecular findings in 12 newly identified families

Human mutation, 2008, Vol.29 (1), p.150-158

2008

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Genetic Defects in TAPT1 Disrupt Ciliogenesis and Cause a Complex Lethal Osteochondrodysplasia

American journal of human genetics, 2015-10, Vol.97 (4), p.521-534

2015

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ACE: adaptive cluster expansion for maximum entropy graphical model inference

Review of interactive digital solutions improving health literacy of personal cancer risks in the general public

Mutations in fibrillin-1 cause congenital scleroderma: stiff skin syndrome

Zebrafish type I collagen mutants faithfully recapitulate human type I collagenopathies

PO-1052 Cyberknife stereotactic radiotherapy for vestibular schwannomas :a single institution experience

Expert consensus for multi-modality imaging evaluation of cardiovascular complications of radiotherapy in adults: a report from the European Association of Cardiovascular Imaging and the American Society of Echocardiography

Hearing loss in Waardenburg syndrome: a systematic review

Recurrent Mutation in the First Zinc Finger of the Orphan Nuclear Receptor NR2E3 Causes Autosomal Dominant Retinitis Pigmentosa

The COVID-19 pandemic : a real opportunity for digital health

Exome sequencing revealed a novel biallelic deletion in the DCAF17 gene underlying Woodhouse Sakati syndrome

Zebrafish Collagen Type I: Molecular and Biochemical Characterization of the Major Structural Protein in Bone and Skin

Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome

A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2

Effect of Mutation Type and Location on Clinical Outcome in 1,013 Probands with Marfan Syndrome or Related Phenotypes and FBN1 Mutations: An International Study

Pharma industry reinvents itself in the turmoil. Part 2. Opportunities

Generation and Validation of a Complete Knockout Model of abcc6a in Zebrafish

TEAD4 regulates trophectoderm differentiation upstream of CDX2 in a GATA3-independent manner in the human preimplantation embryo

Pharma industry reinvents itself in the turmoil. Part 1. Challenges

Mutation detection in the ABCC6 gene and genotype–phenotype analysis in a large international case series affected by pseudoxanthoma elasticum

Cumulus cell gene expression predicts better cleavage-stage embryo or blastocyst development and pregnancy for ICSI patients

Risk management and (health) crisis: How to assess the impact of changing a prescription over time in radiotherapy

The Abcc6a Knockout Zebrafish Model as a Novel Tool for Drug Screening for Pseudoxanthoma Elasticum

Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis

Arterial tortuosity syndrome: clinical and molecular findings in 12 newly identified families

Genetic Defects in TAPT1 Disrupt Ciliogenesis and Cause a Complex Lethal Osteochondrodysplasia

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