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Alexandre Janin

University of Lyon

26

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215

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Characterization of Loss-Of-Function KCNJ2 Mutations in Atypical Andersen Tawil Syndrome

2021 Frontiers in Genetics
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Active transpression along the Owen oceanic transform fault, India - Somalia plate boundary

2021
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Geophysical investigation of the western end of the Carlsberg Ridge: preliminary results of the CARLMAG cruise

2020
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Impact of APOB missense variations on apolipoprotein B secretion: A CRISPR-cas9 model

2020 Atherosclerosis
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Imaging the past and present Owen transform fault: preliminary results from the VARUNA seismic cruise

2020
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Author response for "DEVELOPMENT OF A NEW EXPANDED NEXT‐GENERATION SEQUENCING PANEL FOR GENETIC DISEASES INVOLVED IN DYSLIPIDEMIA"

2020
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Seismic profiles across the North Anatolian Fault in the Aegean Sea

2018 European geosciences union general assembly
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A Novel Missense Mutation p.Gly162Glu of the Gene MYL2 Involved in Hypertrophic Cardiomyopathy: A Pedigree Analysis of a Proband

2018 Molecular Diagnosis & Therapy
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First identification of homozygous truncating CSRP3 variants in two unrelated cases with hypertrophic cardiomyopathy

2018 Gene
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TRPM4 mutations to cause autosomal recessive and not autosomal dominant Brugada type 1 syndrome

2018 European Journal of Medical Genetics
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