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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
	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.
	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
	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
	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
	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
	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
	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
	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
	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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