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Gene-wise association of variants in four lysosomal storage disorder genes in neuropathologically confirmed Lewy body disease.
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Impact of Sixteen Established Pancreatic Cancer Susceptibility Loci in American Jews.
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High-depth whole genome sequencing of an Ashkenazi Jewish reference panel: enhancing sensitivity, accuracy, and imputation.
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Hum Genet
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Novel ultra-rare exonic variants identified in a founder population implicate cadherins in schizophrenia.
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Neuron
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Genome-wide data from medieval German Jews show that the Ashkenazi founder event pre-dated the 14<sup>th</sup> century.
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The predictive capacity of polygenic risk scores for disease risk is only moderately influenced by imputation panels tailored to the target population.
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Bioinformatics
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2024
btae036
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Human Y chromosome haplogroup L1-M22 traces Neolithic expansion in West Asia and supports the Elamite and Dravidian connection.
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iScience
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2024
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