[Molecular analysis of 68 Swiss-Romance subjects at risk for fragile X syndrome]

Reduction in Nuclear Size and Quadrupole Deformation of High-Spin Isomers of ^{127,129}In.

Physical review letters·2025

An asymmetric fission island driven by shell effects in light fragments.

Nature·2025

Evidence for Coexisting Shapes through Lifetime Measurements in ^{98}Zr.

Physical review letters·2018

Prominent Optic Disc Featured in Inherited Retinopathy.

Klinische Monatsblatter fur Augenheilkunde·2017

Preserved functional and structural integrity of the papillomacular area correlates with better visual acuity in retinitis pigmentosa.

Eye (London, England)·2016

A Novel Recessive RPGRIP1 Mutation Causing Leber Congenital Amaurosis.

Klinische Monatsblatter fur Augenheilkunde·2016

Large-scale association study identifies lung cancer susceptibility copy number variants and their potential functional role in genetic instability.

Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology·2026

Disease associations for rare immune genetic variants require statistical or rule-based support.

Journal of human immunity·2026

Protocol for Designing and Interpreting Minigene Assays to Validate Candidate Splice-Altering Variants Using Long-read Sequencing.

Current protocols·2026

Genetics of vasculitis.

Current opinion in rheumatology·2026

First Genetics Association Study of the ACE I/D Polymorphism with Inflammatory Arthropathy Susceptibility in the Western Algerian Population: A Case-Control Study.

Current rheumatology reviews·2026

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[Molecular analysis of 68 Swiss-Romance subjects at risk for fragile X syndrome]

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Reduction in Nuclear Size and Quadrupole Deformation of High-Spin Isomers of ^{127,129}In.

An asymmetric fission island driven by shell effects in light fragments.

Evidence for Coexisting Shapes through Lifetime Measurements in ^{98}Zr.

Prominent Optic Disc Featured in Inherited Retinopathy.

Preserved functional and structural integrity of the papillomacular area correlates with better visual acuity in retinitis pigmentosa.

A Novel Recessive RPGRIP1 Mutation Causing Leber Congenital Amaurosis.

Large-scale association study identifies lung cancer susceptibility copy number variants and their potential functional role in genetic instability.

Disease associations for rare immune genetic variants require statistical or rule-based support.

Protocol for Designing and Interpreting Minigene Assays to Validate Candidate Splice-Altering Variants Using Long-read Sequencing.

Genetics of vasculitis.

First Genetics Association Study of the ACE I/D Polymorphism with Inflammatory Arthropathy Susceptibility in the Western Algerian Population: A Case-Control Study.

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[Molecular analysis of 68 Swiss-Romance subjects at risk for fragile X syndrome]

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