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1 |
Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation
Enthalten in Molecular psychiatry 14.8.2018: 1-17
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2 |
CHCHD 10 mutations promote loss of mitochondrial cristae junctions with impaired mitochondrial genome maintenance and inhibition of apoptosis
Enthalten in European Molecular Biology Organization: EMBO molecular medicine Bd. 8, 2016, Nr. 1: 58-72. 15 S.
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3 |
Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease
Enthalten in Nature genetics Bd. 54, 21.11.2022, Nr. 12, date:12.2022: 1786-1794
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4 |
Genome-wide association study of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Europe
Enthalten in Orphanet journal of rare diseases Bd. 6, 29.7.2011, Nr. 1, date:12.2011: 1-10
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5 |
How local reference panels improve imputation in French populations
Enthalten in Scientific reports Bd. 14, 3.1.2024, Nr. 1, date:12.2024: 1-13
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6 |
Human genetic structure in Northwest France provides new insights into West European historical demography
Enthalten in Nature Communications Bd. 15, 7.8.2024, Nr. 1, date:12.2024: 1-18
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7 |
Identification of potential genetic risk factors for bipolar disorder by whole-exome sequencing
Enthalten in Translational Psychiatry Bd. 8, 5.12.2018, Nr. 1, date:12.2018: 1-7
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8 |
Increased risk of severe COVID-19 in hospitalized patients with SARS-CoV-2 Alpha variant infection: a multicentre matched cohort study
Enthalten in BMC infectious diseases Bd. 22, 13.6.2022, Nr. 1, date:12.2022: 1-9
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9 |
On the use of haplotype phylogeny to detect disease susceptibility loci
Enthalten in BMC genetics Bd. 6, 18.5.2005, Nr. 1, date:12.2005: 1-13
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10 |
Prolonged increase in psychotropic drug use among young women following the COVID-19 pandemic: a French nationwide retrospective study
Enthalten in BMC medicine Bd. 22, 2.7.2024, Nr. 1, date:12.2024: 1-10
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Administration
