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1 |
Upregulation of adenosine A2A receptor in astrocytes is sufficient to trigger hippocampal multicellular dysfunctions and memory deficits
Enthalten in Molecular psychiatry 23.7.2025: 1-15
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2 |
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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3 |
Association of modifiers and other genetic factors explain Marfan syndrome clinical variability
Enthalten in European journal of human genetics 7.8.2018: 1-14
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4 |
A Difficult and Rare Diagnosis of Autoimmune Enteropathy in a Patient Affected by Down Syndrome
Enthalten in Journal of clinical immunology 12.4.2016: 1-6
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5 |
Molecular Evidence of Reproductive Isolation in Sympatric Sibling Species of Mouse Lemurs
Enthalten in International journal of primatology Bd. 23, Nr. 6, date:12.2002: 1335-1343
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6 |
Ameboma: an unusual cause of gastrointestinal bleeding during severe leptospirosis
Enthalten in BMC infectious diseases Bd. 14, 2.6.2014, Nr. 1, date:12.2014: 1-6
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7 |
CA9 gene expression in conventional renal cell carcinoma: a potential marker for prediction of early metastasis after nephrectomy
Enthalten in Clinical & experimental metastasis Bd. 24, 28.3.2007, Nr. 3, date:5.2007: 149-155
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8 |
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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9 |
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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10 |
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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