Inferring CpG methylation signatures accumulated along human history from genetic variation catalogs

por Si, Yichen, Zöllner, Sebastian
Publicado 2023

The effect of mutation subtypes on the allele frequency spectrum and population genetics inference

por Liao, Kevin, Carlson, Jedidiah, Zöllner, Sebastian
Publicado 2023

A Quantitative Comparison of the Similarity between Genes and Geography in Worldwide Human Populations

por Wang, Chaolong, Zöllner, Sebastian, Rosenberg, Noah A.
Publicado 2012

Helmsman: fast and efficient mutation signature analysis for massive sequencing datasets

por Carlson, Jedidiah, Li, Jun Z., Zöllner, Sebastian
Publicado 2018

Genotype Imputation Reference Panel Selection Using Maximal Phylogenetic Diversity

por Zhang, Peng, Zhan, Xiaowei, Rosenberg, Noah A., Zöllner, Sebastian
Publicado 2013

A Coalescent Model for Genotype Imputation

por Jewett, Ethan M., Zawistowski, Matthew, Rosenberg, Noah A., Zöllner, Sebastian
Publicado 2012

Choosing Subsamples for Sequencing Studies by Minimizing the Average Distance to the Closest Leaf

por Kang, Jonathan T. L., Zhang, Peng, Zöllner, Sebastian, Rosenberg, Noah A.
Publicado 2015

Gene-set Enrichment with Mathematical Biology (GEMB)

por Cochran, Amy L, Nieser, Kenneth J, Forger, Daniel B, Zöllner, Sebastian, McInnis, Melvin G
Publicado 2020

Genomewide significance testing of variation from single case exomes

por Wilfert, Amy B., Chao, Katherine R., Kaushal, Madhurima, Jain, Sanjay, Zöllner, Sebastian, Adams, David R., Conrad, Donald F.
Publicado 2016

Analysis of somatic mutations identifies signs of selection during in vitro aging of primary dermal fibroblasts

por Narisu, Narisu, Rothwell, Rebecca, Vrtačnik, Peter, Rodríguez, Sofía, Didion, John, Zöllner, Sebastian, Erdos, Michael R., Collins, Francis S., Eriksson, Maria
Publicado 2019

Comparing variant calling algorithms for target-exon sequencing in a large sample

por Lo, Yancy, Kang, Hyun M, Nelson, Matthew R, Othman, Mohammad I, Chissoe, Stephanie L, Ehm, Margaret G, Abecasis, Gonçalo R, Zöllner, Sebastian
Publicado 2015

First mitochondrial genome-wide association study with metabolomics

por Aboulmaouahib, Brahim, Kastenmüller, Gabi, Suhre, Karsten, Zöllner, Sebastian, Weissensteiner, Hansi, Prehn, Cornelia, Adamski, Jerzy, Gieger, Christian, Wang-Sattler, Rui, Lichtner, Peter, Strauch, Konstantin, Flaquer, Antònia
Publicado 2021

The influence of genomic context on mutation patterns in the human genome inferred from rare variants

por Schaibley, Valerie M., Zawistowski, Matthew, Wegmann, Daniel, Ehm, Margaret G., Nelson, Matthew R., St. Jean, Pamela L., Abecasis, Gonçalo R., Novembre, John, Zöllner, Sebastian, Li, Jun Z.
Publicado 2013

Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans

por Carlson, Jedidiah, Locke, Adam E., Flickinger, Matthew, Zawistowski, Matthew, Levy, Shawn, Myers, Richard M., Boehnke, Michael, Kang, Hyun Min, Scott, Laura J., Li, Jun Z., Zöllner, Sebastian
Publicado 2018

FICTURE: Scalable segmentation-free analysis of submicron resolution spatial transcriptomics

por Si, Yichen, Lee, ChangHee, Hwang, Yongha, Yun, Jeong H., Cheng, Weiqiu, Cho, Chun-Seok, Quiros, Miguel, Nusrat, Asma, Zhang, Weizhou, Jun, Goo, Zöllner, Sebastian, Lee, Jun Hee, Kang, Hyun Min
Publicado 2023

The Michigan Genomics Initiative: A biobank linking genotypes and electronic clinical records in Michigan Medicine patients

por Zawistowski, Matthew, Fritsche, Lars G., Pandit, Anita, Vanderwerff, Brett, Patil, Snehal, Schmidt, Ellen M., VandeHaar, Peter, Willer, Cristen J., Brummett, Chad M., Kheterpal, Sachin, Zhou, Xiang, Boehnke, Michael, Abecasis, Gonçalo R., Zöllner, Sebastian
Publicado 2023

Multi-ancestry meta-analysis identifies 5 novel loci for ischemic stroke and reveals heterogeneity of effects between sexes and ancestries

por Surakka, Ida, Wu, Kuan-Han, Hornsby, Whitney, Wolford, Brooke N., Shen, Fred, Zhou, Wei, Huffman, Jennifer E., Pandit, Anita, Hu, Yao, Brumpton, Ben, Skogholt, Anne Heidi, Gabrielsen, Maiken E., Walters, Robin G., Hveem, Kristian, Kooperberg, Charles, Zöllner, Sebastian, Wilson, Peter W.F., Sutton, Nadia R., Daly, Mark J., Neale, Benjamin M., Willer, Cristen J.
Publicado 2023

Transmission of human mtDNA heteroplasmy in the Genome of the Netherlands families: support for a variable-size bottleneck

por Li, Mingkun, Rothwell, Rebecca, Vermaat, Martijn, Wachsmuth, Manja, Schröder, Roland, Laros, Jeroen F.J., van Oven, Mannis, de Bakker, Paul I.W., Bovenberg, Jasper A., van Duijn, Cornelia M., van Ommen, Gert-Jan B., Slagboom, P. Eline, Swertz, Morris A., Wijmenga, Cisca, Kayser, Manfred, Boomsma, Dorret I., Zöllner, Sebastian, de Knijff, Peter, Stoneking, Mark
Publicado 2016

De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population

por Kessler, Michael D., Loesch, Douglas P., Perry, James A., Heard-Costa, Nancy L., Taliun, Daniel, Cade, Brian E., Wang, Heming, Daya, Michelle, Ziniti, John, Datta, Soma, Celedón, Juan C., Soto-Quiros, Manuel E., Avila, Lydiana, Weiss, Scott T., Barnes, Kathleen, Redline, Susan S., Vasan, Ramachandran S., Johnson, Andrew D., Mathias, Rasika A., Hernandez, Ryan, Wilson, James G., Nickerson, Deborah A., Abecasis, Goncalo, Browning, Sharon R., Zöllner, Sebastian, O’Connell, Jeffrey R., Mitchell, Braxton D., O’Connor, Timothy D.
Publicado 2020

Genome-Wide Association of Bipolar Disorder Suggests an Enrichment of Replicable Associations in Regions near Genes

por Smith, Erin N., Koller, Daniel L., Panganiban, Corrie, Szelinger, Szabolcs, Zhang, Peng, Badner, Judith A., Barrett, Thomas B., Berrettini, Wade H., Bloss, Cinnamon S., Byerley, William, Coryell, William, Edenberg, Howard J., Foroud, Tatiana, Gershon, Elliot S., Greenwood, Tiffany A., Guo, Yiran, Hipolito, Maria, Keating, Brendan J., Lawson, William B., Liu, Chunyu, Mahon, Pamela B., McInnis, Melvin G., McMahon, Francis J., McKinney, Rebecca, Murray, Sarah S., Nievergelt, Caroline M., Nurnberger, John I., Nwulia, Evaristus A., Potash, James B., Rice, John, Schulze, Thomas G., Scheftner, William A., Shilling, Paul D., Zandi, Peter P., Zöllner, Sebastian, Craig, David W., Schork, Nicholas J., Kelsoe, John R.
Publicado 2011