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Feasibility, pitfalls and results of a structured concept-development phase for a randomized controlled phase III trial on radiotherapy in primary prostate cancer patients

BMC cancer, 2022-03, Vol.22 (1), p.337-337, Article 337

2022

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A segmental maximum a posteriori approach to genome-wide copy number profiling

Bioinformatics, 2008-03, Vol.24 (6), p.751-758

2008

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Somatic mosaicism for copy number variation in differentiated human tissues

Human mutation, 2008-09, Vol.29 (9), p.1118-1124

2008

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Sexual function of men undergoing single prostate cancer treatment – results of the EUPROMS study

European urology open science (Online), 2020-11, Vol.21, p.S130-S131

2020

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Characterization of novel and complex genomic aberrations in glioblastoma using a 32K BAC array

Neuro-oncology (Charlottesville, Va.), 2009-12, Vol.11 (6), p.803-818

2009

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Profiling of copy number variations (CNVs) in healthy individuals from three ethnic groups using a human genome 32 K BAC-clone-based array

Human mutation, 2008-03, Vol.29 (3), p.398-408

2008

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Distal 22q11.2 microduplication encompassing the BCR gene

American journal of medical genetics. Part A, 2008-12, Vol.146A (23), p.3075-3081

2008

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The impact of prostate cancer ADT and EBRT follow-up treatment on patient-reported quality of life – results from the EUPROMS 2.0 follow-up study

European urology, 2024-03, Vol.85, p.S672-S673

2024

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A0001 - The impact of prostate cancer ADT and EBRT follow-up treatment on patient-reported quality of life – results from the EUPROMS 2.0 follow-up study

European urology, 2024-03, Vol.85, p.S672-S673

2024

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A previously unrecognized microdeletion syndrome on chromosome 22 band q11.2 encompassing the BCR gene

American journal of medical genetics. Part A, 2007-09, Vol.143A (18), p.2178-2184

2007

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Quality of life for higher vs. lower educated men following active surveillance, radical prostatectomy or radiotherapy in the patient-initiated EUPROMS study

European urology, 2022-02, Vol.81, p.S442-S443

2022

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Sexual function of men undergoing invasive prostate cancer treatment versus active surveillance – Results of the EUPROMS study

European urology, 2021-06, Vol.79, p.S1483-S1484

2021

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684P The real effects of prostate cancer chemotherapy: Results of the EUPROMs prostate patient-driven quality of life study

Annals of oncology, 2020-09, Vol.31, p.S544-S544

2020

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A patient with 22q11.2 deletion and Opitz syndrome‐like phenotype has the same deletion as velocardiofacial patients

American journal of medical genetics. Part A, 2007-12, Vol.143A (24), p.3302-3308

2007

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Strong conservation of the human NF2 locus based on sequence comparison in five species

Mammalian genome, 2003-08, Vol.14 (8), p.526-536

2003

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Gene expression profiling shows that macrophages derived from mouse embryonic stem cells is an improved in vitro model for studies of vascular disease

Experimental cell research, 2004-11, Vol.300 (2), p.335-344

2004

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Fine mapping of the constitutional translocation t(11;22)(q23;q11)

Human genetics, 2000-05, Vol.106 (5), p.506-516

2000

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A group of schwannomas with interstitial deletions on 22q located outside the NF2 locus shows no detectable mutations in the NF2 gene

Human genetics, 1999-05, Vol.104 (5), p.418-424

1999

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Profiling of copy number variations (CNVs) in healthy individuals from three ethnic groups using a human genome 32K BAC-clone-based array

Human mutation, 2008-03, Vol.29 (3), p.398-408

2008

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No evidence demonstrating hepatotoxicity associated with hydroxycitric acid

World journal of gastroenterology : WJG, 2009-08, Vol.15 (32), p.4087-4089

2009

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In vivo and ex vivo confocal endomicroscopy of pancreatic cystic lesions: A prospective study

World journal of gastroenterology : WJG, 2017-05, Vol.23 (18), p.3338-3348

2017

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Pore Scale Geochemical Processes

1, 2015

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Feasibility, pitfalls and results of a structured concept-development phase for a randomized controlled phase III trial on radiotherapy in primary prostate cancer patients

A segmental maximum a posteriori approach to genome-wide copy number profiling

Somatic mosaicism for copy number variation in differentiated human tissues

Sexual function of men undergoing single prostate cancer treatment – results of the EUPROMS study

Characterization of novel and complex genomic aberrations in glioblastoma using a 32K BAC array

Profiling of copy number variations (CNVs) in healthy individuals from three ethnic groups using a human genome 32 K BAC-clone-based array

Distal 22q11.2 microduplication encompassing the BCR gene

The impact of prostate cancer ADT and EBRT follow-up treatment on patient-reported quality of life – results from the EUPROMS 2.0 follow-up study

A0001 - The impact of prostate cancer ADT and EBRT follow-up treatment on patient-reported quality of life – results from the EUPROMS 2.0 follow-up study

A previously unrecognized microdeletion syndrome on chromosome 22 band q11.2 encompassing the BCR gene

Quality of life for higher vs. lower educated men following active surveillance, radical prostatectomy or radiotherapy in the patient-initiated EUPROMS study

Sexual function of men undergoing invasive prostate cancer treatment versus active surveillance – Results of the EUPROMS study

684P The real effects of prostate cancer chemotherapy: Results of the EUPROMs prostate patient-driven quality of life study

A patient with 22q11.2 deletion and Opitz syndrome‐like phenotype has the same deletion as velocardiofacial patients

Strong conservation of the human NF2 locus based on sequence comparison in five species

A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications

Gene expression profiling shows that macrophages derived from mouse embryonic stem cells is an improved in vitro model for studies of vascular disease

Fine mapping of the constitutional translocation t(11;22)(q23;q11)

A group of schwannomas with interstitial deletions on 22q located outside the NF2 locus shows no detectable mutations in the NF2 gene

Profiling of copy number variations (CNVs) in healthy individuals from three ethnic groups using a human genome 32K BAC-clone-based array

A full-coverage, high-resolution human chromosome 22 genomic microarrayfor clinical and research applications

No evidence demonstrating hepatotoxicity associated with hydroxycitric acid

High resolution deletion analysis of conctitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH

In vivo and ex vivo confocal endomicroscopy of pancreatic cystic lesions: A prospective study

Pore Scale Geochemical Processes

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