Personal profile
Expertise related to UN Sustainable Development Goals
In 2015, UN member states agreed to 17 global Sustainable Development Goals (SDGs) to end poverty, protect the planet and ensure prosperity for all. This person’s work contributes towards the following SDG(s):
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SDG 3 Good Health and Well-being
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Dive into the research topics where Andrew Klaus Sobering is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Collaborations and top research areas from the last five years
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
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Insights into ancestral diversity in Parkinson’s disease risk: a comparative assessment of polygenic risk scores
the 23andMe Research Team & Global Parkinson’s Genetics Program (GP2), Dec 2025, In: npj Parkinson's Disease. 11, 1, 201.Research output: Contribution to journal › Article › peer-review
Open Access3 Link opens in a new tab Scopus citations -
The LRRK2 p.L1795F variant causes Parkinson’s disease in the European population
the Global Parkinson’s Genetics Program (GP2), Dec 2025, In: npj Parkinson's Disease. 11, 1, 58.Research output: Contribution to journal › Article › peer-review
Open Access2 Link opens in a new tab Scopus citations -
TMEM175, SCARB2 and CTSB associations with Parkinson’s disease risk across populations
the Global Parkinson’s Genetic Program (GP2), Dec 2025, In: npj Parkinson's Disease. 11, 1, 348.Research output: Contribution to journal › Article › peer-review
Open Access1 Link opens in a new tab Scopus citations -
Two New Cases Expand the Phenotypic Spectrum of TUBG1 Missense Variants
Urreizti, R., Vissicchio, J., Idries, M., Cozar, M., Rabionet, R., Donald, T., Bhoj, E. J., Nomakuchi, T. T., Shipley, S. C., Timms, A. E., Mirzaa, G. M., Serrano, M. & Sobering, A. K., Sep 2025, In: American Journal of Medical Genetics, Part A. 197, 9, e64095.Research output: Contribution to journal › Article › peer-review
Open Access -
Expanding the clinical phenotype and variant spectrum associated with RFX7
Sisroe, T., Santos, A. D., Rippert, A. L., Gray, C., Skraban, C. M., Nelson, B., Tefft, S., Helbig, I., Li, D., Bhoj, E. J. & Sobering, A. K., Dec 2024, In: American Journal of Medical Genetics, Part A. 194, 12, e63816.Research output: Contribution to journal › Article › peer-review
Open Access