Canlyniadau Chwilio - Prokopenko, Dmitry

Parallel multiplex thermodynamic analysis of coaxial base stacking in DNA duplexes by oligodeoxyribonucleotide microchips gan Vasiliskov, Vadim A., Prokopenko, Dmitry V., Mirzabekov, Andrei D.

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PolyGEE: a generalized estimating equation approach to the efficient and robust estimation of polygenic effects in large-scale association studies gan Hecker, Julian, Prokopenko, Dmitry, Lange, Christoph, Fier, Heide Loehlein

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Reporting Correct p Values in VEGAS Analyses gan Hecker, Julian, Maaser, Anna, Prokopenko, Dmitry, Fier, Heide Loehlein, Lange, Christoph

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Massive parallel analysis of the binding specificity of histone-like protein HU to single- and double-stranded DNA with generic oligodeoxyribonucleotide microchips gan Krylov, Alexander S., Zasedateleva, Olga A., Prokopenko, Dmitry V., Rouviere-Yaniv, Josette, Mirzabekov, Andrei D.

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Reply to Neupane et al.: Replication study of AD‐associated rare variants gan Prokopenko, Dmitry, Morgan, Sarah L., Lange, Christoph, Hide, Winston, Bertram, Lars, Tanzi, Rudolph E.

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Using Network Methodology to Infer Population Substructure gan Prokopenko, Dmitry, Hecker, Julian, Silverman, Edwin, Nöthen, Markus M., Schmid, Matthias, Lange, Christoph, Loehlein Fier, Heide

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Estimating the effective sample size in association studies of quantitative traits gan Ziyatdinov, Andrey, Kim, Jihye, Prokopenko, Dmitry, Privé, Florian, Laporte, Fabien, Loh, Po-Ru, Kraft, Peter, Aschard, Hugues

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Utilizing the Jaccard index to reveal population stratification in sequencing data: a simulation study and an application to the 1000 Genomes Project gan Prokopenko, Dmitry, Hecker, Julian, Silverman, Edwin K., Pagano, Marcello, Nöthen, Markus M., Dina, Christian, Lange, Christoph, Fier, Heide Loehlein

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locStra: Fast analysis of regional/global stratification in whole-genome sequencing studies gan Hahn, Georg, Lutz, Sharon M., Hecker, Julian, Prokopenko, Dmitry, Cho, Michael H., Silverman, Edwin K., Weiss, Scott T., Lange, Christoph

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On the association analysis of genome-sequencing data: A spatial clustering approach for partitioning the entire genome into nonoverlapping windows gan Fier, Heide Loehlein, Prokopenko, Dmitry, Hecker, Julian, Cho, Michael H., Silverman, Edwin K., Weiss, Scott T., Tanzi, Rudolph E., Lange, Christoph

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A Smoothed Version of the Lassosum Penalty for Fitting Integrated Risk Models Using Summary Statistics or Individual-Level Data gan Hahn, Georg, Prokopenko, Dmitry, Lutz, Sharon M., Mullin, Kristina, Tanzi, Rudolph E., Cho, Michael H., Silverman, Edwin K., Lange, Christoph

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Most Pathways Can Be Related to the Pathogenesis of Alzheimer’s Disease gan Morgan, Sarah L., Naderi, Pourya, Koler, Katjuša, Pita-Juarez, Yered, Prokopenko, Dmitry, Vlachos, Ioannis S., Tanzi, Rudolph E., Bertram, Lars, Hide, Winston A.

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Gel-based oligonucleotide microarray approach to analyze protein–ssDNA binding specificity gan Zasedateleva, Olga A., Mikheikin, Andrey L., Turygin, Alexander Y., Prokopenko, Dmitry V., Chudinov, Alexander V., Belobritskaya, Elena E., Chechetkin, Vladimir R., Zasedatelev, Alexander S.

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‘Location, Location, Location’: a spatial approach for rare variant analysis and an application to a study on non-syndromic cleft lip with or without cleft palate gan Fier, Heide, Won, Sungho, Prokopenko, Dmitry, AlChawa, Taofik, Ludwig, Kerstin U., Fimmers, Rolf, Silverman, Edwin K., Pagano, Marcello, Mangold, Elisabeth, Lange, Christoph

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Gga3 deletion and a GGA3 rare variant associated with late onset Alzheimer’s disease trigger BACE1 accumulation in axonal swellings gan Lomoio, Selene, Willen, Rachel, Kim, WonHee, Ho, Kevin Z., Robinson, Edward K., Prokopenko, Dmitry, Kennedy, Matthew E., Tanzi, Rudolph E., Tesco, Giuseppina

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An APP ectodomain mutation outside of the Aβ domain promotes Aβ production in vitro and deposition in vivo gan Zhang, Xulun, Zhang, Can Martin, Prokopenko, Dmitry, Liang, Yingxia, Zhen, Sherri Y., Weigle, Ian Q., Han, Weinong, Aryal, Manish, Tanzi, Rudolph E., Sisodia, Sangram S.

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PILRA polymorphism modifies the effect of APOE4 and GM17 on Alzheimer’s disease risk gan Lopatko Lindman, Karin, Jonsson, Caroline, Weidung, Bodil, Olsson, Jan, Pandey, Janardan P., Prokopenko, Dmitry, Tanzi, Rudolph E., Hallmans, Göran, Eriksson, Sture, Elgh, Fredrik, Lövheim, Hugo

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Whole-genome sequencing reveals new Alzheimer’s disease-associated rare variants in loci related to synaptic function and neuronal development gan Prokopenko, Dmitry, Morgan, Sarah L., Mullin, Kristina, Hofmann, Oliver, Chapman, Brad, Kirchner, Rory, Amberkar, Sandeep, Wohlers, Inken, Lange, Christoph, Hide, Winston, Bertram, Lars, Tanzi, Rudolph E.

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Whole‐genome sequencing reveals new Alzheimer's disease–associated rare variants in loci related to synaptic function and neuronal development gan Prokopenko, Dmitry, Morgan, Sarah L., Mullin, Kristina, Hofmann, Oliver, Chapman, Brad, Kirchner, Rory, Amberkar, Sandeep, Wohlers, Inken, Lange, Christoph, Hide, Winston, Bertram, Lars, Tanzi, Rudolph E.

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Identification of Novel Alzheimer’s Disease Loci Using Sex-Specific Family-Based Association Analysis of Whole-Genome Sequence Data gan Prokopenko, Dmitry, Hecker, Julian, Kirchner, Rory, Chapman, Brad A., Hoffman, Oliver, Mullin, Kristina, Hide, Winston, Bertram, Lars, Laird, Nan, DeMeo, Dawn L., Lange, Christoph, Tanzi, Rudolph E.

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