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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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Hearing loss in Waardenburg syndrome: a systematic review

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

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 fibrillin-1 cause congenital scleroderma: stiff skin syndrome

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

2010

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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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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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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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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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Assisted oocyte activation does not overcome recurrent embryo developmental problems

Human reproduction (Oxford), 2023-05, Vol.38 (5), p.872-885

2023

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Germline nuclear transfer in mice may rescue poor embryo development associated with advanced maternal age and early embryo arrest

Human reproduction (Oxford), 2020-07, Vol.35 (7), p.1562-1577

2020

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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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Comparative analysis of mouse and human preimplantation development following POU5F1 CRISPR/Cas9 targeting reveals interspecies differences

Human reproduction (Oxford), 2021-04, Vol.36 (5), p.1242-1252

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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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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Various repair events following CRISPR/Cas9-based mutational correction of an infertility-related mutation in mouse embryos

Journal of assisted reproduction and genetics, 2024-06, Vol.41 (6), p.1605-1617

2024

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Recessive osteogenesis imperfecta caused by LEPRE1 mutations: clinical documentation and identification of the splice form responsible for prolyl 3-hydroxylation

Journal of medical genetics, 2009-04, Vol.46 (4), p.233-241

2009

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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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Feasibility study: The medical imaging as a tool for therapeutic education in radiotherapy

Cancer radiothérapie, 2022-11, Vol.26 (8), p.1034-1044

2022

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The new Ghent criteria for Marfan syndrome: what do they change?

Clinical genetics, 2012-05, Vol.81 (5), p.433-442

2012

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Impact of the use of Luminette® on well-being at work in a radiotherapy department

Cancer radiothérapie, 2013-12, Vol.17 (8), p.731-735

2013

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Total absence of the alpha2(I) chain of collagen type I causes a rare form of Ehlers-Danlos syndrome with hypermobility and propensity to cardiac valvular problems

Journal of medical genetics, 2006-07, Vol.43 (7), p.e36

2006

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Mutations in the KCNQ4 Gene Are Responsible for Autosomal Dominant Deafness in Four DFNA2 Families

Human molecular genetics, 1999-07, Vol.8 (7), p.1321-1328

1999

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PO-0844: Dosimetrical advantages of 4D mid-vent: should every LA NSCLC patient be treated this way?

Radiotherapy and oncology, 2016-04, Vol.119, p.S401-S402

2016

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EP-1366: Hypofractionated prostate EBRT with simultaneously integrated boost: mono-institutional report

Radiotherapy and oncology, 2016-04, Vol.119, p.S637-S638

2016

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Actual Delivered Dose for CTV and Bladder During External Beam Radiation Therapy of Locally Advanced Cervical Cancer: Deformable Dose Accumulation Quality Assurance and Results

International journal of radiation oncology, biology, physics, 2016-10, Vol.96 (2), p.E319-E320

2016

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

Hearing loss in Waardenburg syndrome: a systematic review

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

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

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

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

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

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

Assisted oocyte activation does not overcome recurrent embryo developmental problems

Germline nuclear transfer in mice may rescue poor embryo development associated with advanced maternal age and early embryo arrest

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

Comparative analysis of mouse and human preimplantation development following POU5F1 CRISPR/Cas9 targeting reveals interspecies differences

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

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

Various repair events following CRISPR/Cas9-based mutational correction of an infertility-related mutation in mouse embryos

Recessive osteogenesis imperfecta caused by LEPRE1 mutations: clinical documentation and identification of the splice form responsible for prolyl 3-hydroxylation

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

Feasibility study: The medical imaging as a tool for therapeutic education in radiotherapy

The new Ghent criteria for Marfan syndrome: what do they change?

Impact of the use of Luminette® on well-being at work in a radiotherapy department

Total absence of the alpha2(I) chain of collagen type I causes a rare form of Ehlers-Danlos syndrome with hypermobility and propensity to cardiac valvular problems

Mutations in the KCNQ4 Gene Are Responsible for Autosomal Dominant Deafness in Four DFNA2 Families

PO-0844: Dosimetrical advantages of 4D mid-vent: should every LA NSCLC patient be treated this way?

EP-1366: Hypofractionated prostate EBRT with simultaneously integrated boost: mono-institutional report

Actual Delivered Dose for CTV and Bladder During External Beam Radiation Therapy of Locally Advanced Cervical Cancer: Deformable Dose Accumulation Quality Assurance and Results

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