Two-parameter characterization of chromosome-scale recombination rate

Por Li, Wentian, Freudenberg, Jan
Publicado em 2009

Mappability and read length

Por Li, Wentian, Freudenberg, Jan
Publicado no Front Genet (2014)

Diminishing return for increased Mappability with longer sequencing reads: implications of the k-mer distributions in the human genome

Por Li, Wentian, Freudenberg, Jan, Miramontes, Pedro
Publicado em 2014

Enrichment of Genetic Variants for Rheumatoid Arthritis within T-Cell and NK-Cell Enhancer Regions

Por Freudenberg, Jan, Gregersen, Peter, Li, Wentian
Publicado no Mol Med (2015)

Partial correlation analysis indicates causal relationships between GC-content, exon density and recombination rate in the human genome

Por Freudenberg, Jan, Wang, Mingyi, Yang, Yaning, Li, Wentian
Publicado em 2009

A Simple Method for Analyzing Exome Sequencing Data Shows Distinct Levels of Nonsynonymous Variation for Human Immune and Nervous System Genes

Por Freudenberg, Jan, Gregersen, Peter K., Freudenberg-Hua, Yun
Publicado em 2012

Single Nucleotide Variation Analysis in 65 Candidate Genes for CNS Disorders in a Representative Sample of the European Population

Por Freudenberg-Hua, Yun, Freudenberg, Jan, Kluck, Nadine, Cichon, Sven, Propping, Peter, Nöthen, Markus M.
Publicado em 2003

Locus category based analysis of a large genome-wide association study of rheumatoid arthritis

Por Freudenberg, Jan, Lee, Annette T., Siminovitch, Katherine A., Amos, Christopher I., Ballard, David, Li, Wentian, Gregersen, Peter K.
Publicado em 2010

Absolute pitch exhibits phenotypic and genetic overlap with synesthesia

Por Gregersen, Peter K., Kowalsky, Elena, Lee, Annette, Baron-Cohen, Simon, Fisher, Simon E., Asher, Julian E., Ballard, David, Freudenberg, Jan, Li, Wentian
Publicado no Hum Mol Genet (2013)

Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness

Por Hillmer, Axel M., Freudenberg, Jan, Myles, Sean, Herms, Stefan, Tang, Kun, Hughes, David A., Brockschmidt, Felix F., Ruan, Yijun, Stoneking, Mark, Nöthen, Markus M.
Publicado em 2009

Differential burden of rare protein truncating variants in Alzheimer’s disease patients compared to centenarians

Por Freudenberg-Hua, Yun, Li, Wentian, Abhyankar, Avinash, Vacic, Vladimir, Cortes, Vanessa, Ben-Avraham, Danny, Koppel, Jeremy, Greenwald, Blaine, Germer, Soren, Darnell, Robert B., Barzilai, Nir, Freudenberg, Jan, Atzmon, Gil, Davies, Peter
Publicado no Hum Mol Genet (2016)

Refining the association of MHC with multiple sclerosis in African Americans

Por McElroy, Joseph P., Cree, Bruce A. C., Caillier, Stacy J., Gregersen, Peter K., Herbert, Joseph, Khan, Omar A., Freudenberg, Jan, Lee, Annette, Bridges, S. Louis, Hauser, Stephen L., Oksenberg, Jorge R., Gourraud, Pierre-Antoine
Publicado em 2010

Transancestral mapping of the MHC region in systemic lupus erythematosus identifies new independent and interacting loci at MSH5, HLA-DPB1 and HLA-G

Por Fernando, Michelle M A, Freudenberg, Jan, Lee, Annette, Morris, David Lester, Boteva, Lora, Rhodes, Benjamin, Gonzalez-Escribano, María Francisca, Lopez-Nevot, Miguel Angel, Navarra, Sandra V, Gregersen, Peter K, Martin, Javier, Vyse, Timothy J
Publicado em 2012

Disease variants in genomes of 44 centenarians

Por Freudenberg-Hua, Yun, Freudenberg, Jan, Vacic, Vladimir, Abhyankar, Avinash, Emde, Anne-Katrin, Ben-Avraham, Danny, Barzilai, Nir, Oschwald, Dayna, Christen, Erika, Koppel, Jeremy, Greenwald, Blaine, Darnell, Robert B, Germer, Soren, Atzmon, Gil, Davies, Peter
Publicado em 2014

Five amino acids in three HLA proteins explain most of the association between MHC and seropositive rheumatoid arthritis

Por Raychaudhuri, Soumya, Sandor, Cynthia, Stahl, Eli A., Freudenberg, Jan, Lee, Hye-Soon, Jia, Xiaoming, Alfredsson, Lars, Padyukov, Leonid, Klareskog, Lars, Worthington, Jane, Siminovitch, Katherine A., Bae, Sang-Cheol, Plenge, Robert M., Gregersen, Peter K., de Bakker, Paul I.W.
Publicado em 2012

The DTNBP1 (Dysbindin) Gene Contributes to Schizophrenia, Depending on Family History of the Disease

Por Van Den Bogaert, Ann, Schumacher, Johannes, Schulze, Thomas G., Otte, Andreas C., Ohlraun, Stephanie, Kovalenko, Svetlana, Becker, Tim, Freudenberg, Jan, Jönsson, Erik G., Mattila-Evenden, Marja, Sedvall, Göran C., Czerski, Piotr M., Kapelski, Pawel, Hauser, Joanna, Maier, Wolfgang, Rietschel, Marcella, Propping, Peter, Nöthen, Markus M., Cichon, Sven
Publicado em 2003

Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia

Por Hillmer, Axel M. , Hanneken, Sandra , Ritzmann, Sibylle , Becker, Tim , Freudenberg, Jan , Brockschmidt, Felix F. , Flaquer, Antonia , Freudenberg-Hua, Yun , Jamra, Rami Abou , Metzen, Christine , Heyn, Uwe , Schweiger, Nadine , Betz, Regina C. , Blaumeiser, Bettina , Hampe, Jochen , Schreiber, Stefan , Schulze, Thomas G. , Hennies, Hans Christian , Schumacher, Johannes , Propping, Peter , Ruzicka, Thomas , Cichon, Sven , Wienker, Thomas F. , Kruse, Roland , Nöthen, Markus M. 
Publicado em 2005

Use of a Multiethnic Approach to Identify Rheumatoid- Arthritis-Susceptibility Loci, 1p36 and 17q12

Por Kurreeman, Fina A.S., Stahl, Eli A., Okada, Yukinori, Liao, Katherine, Diogo, Dorothée, Raychaudhuri, Soumya, Freudenberg, Jan, Kochi, Yuta, Patsopoulos, Nikolaos A., Gupta, Namrata, Sandor, Cynthia, Bang, So-Young, Lee, Hye-Soon, Padyukov, Leonid, Suzuki, Akari, Siminovitch, Kathy, Worthington, Jane, Gregersen, Peter K., Hughes, Laura B., Reynolds, Richard J., Bridges, S. Louis, Bae, Sang-Cheol, Yamamoto, Kazuhiko, Plenge, Robert M.
Publicado em 2012

C9orf72 ablation causes immune dysregulation characterized by leukocyte expansion, autoantibody production, and glomerulonephropathy in mice

Por Atanasio, Amanda, Decman, Vilma, White, Derek, Ramos, Meg, Ikiz, Burcin, Lee, Hoi-Ching, Siao, Chia-Jen, Brydges, Susannah, LaRosa, Elizabeth, Bai, Yu, Fury, Wen, Burfeind, Patricia, Zamfirova, Ralica, Warshaw, Gregg, Orengo, Jamie, Oyejide, Adelekan, Fralish, Michael, Auerbach, Wojtek, Poueymirou, William, Freudenberg, Jan, Gong, Guochun, Zambrowicz, Brian, Valenzuela, David, Yancopoulos, George, Murphy, Andrew, Thurston, Gavin, Lai, Ka-Man Venus
Publicado no Sci Rep (2016)

CSK regulatory polymorphism is associated with systemic lupus erythematosus and influences B cell signaling and activation

Por Manjarrez-Orduño, Nataly, Marasco, Emiliano, Chung, Sharon A., Katz, Matthew S., Kiridly, Jenna F., Simpfendorfer, Kim R., Freudenberg, Jan, Ballard, David H., Nashi, Emil, Hopkins, Thomas J., Graham, Deborah S Cunninghame, Lee, Annette T., Coenen, Marieke J. H., Franke, Barbara, Swinkels, Dorine W., Graham, Robert R., Kimberly, Robert P., Gaffney, Patrick M., Vyse, Timothy J., Behrens, Timothy W., Criswell, Lindsey A., Diamond, Betty, Gregersen, Peter K.
Publicado em 2012