ClubSub-P: Cluster-Based Subcellular Localization Prediction for Gram-Negative Bacteria and Archaea

Por Paramasivam, Nagarajan, Linke, Dirk
Publicado em 2011

Is the C-terminal insertional signal in Gram-negative bacterial outer membrane proteins species-specific or not?

Por Paramasivam, Nagarajan, Habeck, Michael, Linke, Dirk
Publicado em 2012

Pedigree based DNA sequencing pipeline for germline genomes of cancer families

Por Försti, Asta, Kumar, Abhishek, Paramasivam, Nagarajan, Schlesner, Matthias, Catalano, Calogerina, Dymerska, Dagmara, Lubinski, Jan, Eils, Roland, Hemminki, Kari
Publicado no Hered Cancer Clin Pract (2016)

SIPA1L3 identified by linkage analysis and whole-exome sequencing as a novel gene for autosomal recessive congenital cataract

Por Evers, Christina, Paramasivam, Nagarajan, Hinderhofer, Katrin, Fischer, Christine, Granzow, Martin, Schmidt-Bacher, Annette, Eils, Roland, Steinbeisser, Herbert, Schlesner, Matthias, Moog, Ute
Publicado no Eur J Hum Genet (2015)

Familial Cancer Variant Prioritization Pipeline version 2 (FCVPPv2) applied to a papillary thyroid cancer family

Por Kumar, Abhishek, Bandapalli, Obul Reddy, Paramasivam, Nagarajan, Giangiobbe, Sara, Diquigiovanni, Chiara, Bonora, Elena, Eils, Roland, Schlesner, Matthias, Hemminki, Kari, Försti, Asta
Publicado no Sci Rep (2018)

A Germline Mutation in the POT1 Gene Is a Candidate for Familial Non-Medullary Thyroid Cancer

Por Srivastava, Aayushi, Miao, Beiping, Skopelitou, Diamanto, Kumar, Varun, Kumar, Abhishek, Paramasivam, Nagarajan, Bonora, Elena, Hemminki, Kari, Försti, Asta, Bandapalli, Obul Reddy
Publicado no Cancers (Basel) (2020)

Whole Genome Sequencing Prioritizes CHEK2, EWSR1, and TIAM1 as Possible Predisposition Genes for Familial Non-Medullary Thyroid Cancer

Por Srivastava, Aayushi, Giangiobbe, Sara, Skopelitou, Diamanto, Miao, Beiping, Paramasivam, Nagarajan, Diquigiovanni, Chiara, Bonora, Elena, Hemminki, Kari, Försti, Asta, Bandapalli, Obul Reddy
Publicado no Front Endocrinol (Lausanne) (2021)

Identification of Familial Hodgkin Lymphoma Predisposing Genes Using Whole Genome Sequencing

Por Srivastava, Aayushi, Giangiobbe, Sara, Kumar, Abhishek, Paramasivam, Nagarajan, Dymerska, Dagmara, Behnisch, Wolfgang, Witzens-Harig, Mathias, Lubinski, Jan, Hemminki, Kari, Försti, Asta, Bandapalli, Obul Reddy
Publicado no Front Bioeng Biotechnol (2020)

Cancer Predisposition Genes in Cancer-Free Families

Por Zheng, Guoqiao, Catalano, Calogerina, Bandapalli, Obul Reddy, Paramasivam, Nagarajan, Chattopadhyay, Subhayan, Schlesner, Matthias, Sijmons, Rolf, Hemminki, Akseli, Dymerska, Dagmara, Lubinski, Jan, Hemminki, Kari, Försti, Asta
Publicado no Cancers (Basel) (2020)

A rare large duplication of MLH1 identified in Lynch syndrome

Por Kumar, Abhishek, Paramasivam, Nagarajan, Bandapalli, Obul Reddy, Schlesner, Matthias, Chen, Tianhui, Sijmons, Rolf, Dymerska, Dagmara, Golebiewska, Katarzyna, Kuswik, Magdalena, Lubinski, Jan, Hemminki, Kari, Försti, Asta
Publicado no Hered Cancer Clin Pract (2021)

Whole Exome Sequencing Identifies APCDD1 and HDAC5 Genes as Potentially Cancer Predisposing in Familial Colorectal Cancer

Por Skopelitou, Diamanto, Miao, Beiping, Srivastava, Aayushi, Kumar, Abhishek, Kuswick, Magdalena, Dymerska, Dagmara, Paramasivam, Nagarajan, Schlesner, Matthias, Lubinski, Jan, Hemminki, Kari, Försti, Asta, Bandapalli, Obul Reddy
Publicado no Int J Mol Sci (2021)

A Novel Low-Risk Germline Variant in the SH2 Domain of the SRC Gene Affects Multiple Pathways in Familial Colorectal Cancer

Por Skopelitou, Diamanto, Miao, Beiping, Srivastava, Aayushi, Kumar, Abhishek, Kuświk, Magdalena, Dymerska, Dagmara, Paramasivam, Nagarajan, Schlesner, Matthias, Lubiński, Jan, Hemminki, Kari, Försti, Asta, Bandapalli, Obul Reddy
Publicado no J Pers Med (2021)

The Frog Xenopus as a Model to Study Joubert Syndrome: The Case of a Human Patient With Compound Heterozygous Variants in PIBF1

Por Ott, Tim, Kaufmann, Lilian, Granzow, Martin, Hinderhofer, Katrin, Bartram, Claus R., Theiß, Susanne, Seitz, Angelika, Paramasivam, Nagarajan, Schulz, Angela, Moog, Ute, Blum, Martin, Evers, Christina M.
Publicado no Front Physiol (2019)

Segregation and potential functional impact of a rare stop-gain PABPC4L variant in familial atypical Parkinsonism

Por Aslam, Muhammad, Ullah, Anwar, Paramasivam, Nagarajan, Kandasamy, Nirosiya, Naureen, Saima, Badshah, Mazhar, Khan, Kafaitullah, Wajid, Muhammad, Abbasi, Rashda, Eils, Roland, Brockmann, Marc A., Schlesner, Matthias, Ahmad, Nafees, von Engelhardt, Jakob
Publicado no Sci Rep (2019)

TALEN/CRISPR-mediated engineering of a promoterless anti-viral RNAi hairpin into an endogenous miRNA locus

Por Senís, Elena, Mockenhaupt, Stefan, Rupp, Daniel, Bauer, Tobias, Paramasivam, Nagarajan, Knapp, Bettina, Gronych, Jan, Grosse, Stefanie, Windisch, Marc P., Schmidt, Florian, Theis, Fabian J., Eils, Roland, Lichter, Peter, Schlesner, Matthias, Bartenschlager, Ralf, Grimm, Dirk
Publicado no Nucleic Acids Res (2017)

A novel homozygous ARL13B variant in patients with Joubert syndrome impairs its guanine nucleotide-exchange factor activity

Por Rafiullah, Rafiullah, Long, Alyssa B., Ivanova, Anna A., Ali, Hazrat, Berkel, Simone, Mustafa, Ghulam, Paramasivam, Nagarajan, Schlesner, Matthias, Wiemann, Stefan, Wade, Rebecca C., Bolthauser, Eugen, Blum, Martin, Kahn, Richard A., Caspary, Tamara, Rappold, Gudrun A.
Publicado no Eur J Hum Genet (2017)

Putative second hit rare genetic variants in families with seemingly GBA-associated Parkinson’s disease

Por Aslam, Muhammad, Kandasamy, Nirosiya, Ullah, Anwar, Paramasivam, Nagarajan, Öztürk, Mehmet Ali, Naureen, Saima, Arshad, Abida, Badshah, Mazhar, Khan, Kafaitullah, Wajid, Muhammad, Abbasi, Rashda, Ilyas, Muhammad, Eils, Roland, Schlesner, Matthias, Wade, Rebecca C., Ahmad, Nafees, von Engelhardt, Jakob
Publicado no NPJ Genom Med (2021)

Characterization of rare germline variants in familial multiple myeloma

Por Catalano, Calogerina, Paramasivam, Nagarajan, Blocka, Joanna, Giangiobbe, Sara, Huhn, Stefanie, Schlesner, Matthias, Weinhold, Niels, Sijmons, Rolf, de Jong, Mirjam, Langer, Christian, Preuss, Klaus-Dieter, Nilsson, Björn, Durie, Brian, Goldschmidt, Hartmut, Bandapalli, Obul Reddy, Hemminki, Kari, Försti, Asta
Publicado no Blood Cancer J (2021)

Genetic subclone architecture of tumor clone-initiating cells in colorectal cancer

Por Giessler, Klara M., Kleinheinz, Kortine, Huebschmann, Daniel, Balasubramanian, Gnana Prakash, Dubash, Taronish D., Dieter, Sebastian M., Siegl, Christine, Herbst, Friederike, Weber, Sarah, Hoffmann, Christopher M., Fronza, Raffaele, Buchhalter, Ivo, Paramasivam, Nagarajan, Eils, Roland, Schmidt, Manfred, von Kalle, Christof, Schneider, Martin, Ulrich, Alexis, Scholl, Claudia, Fröhling, Stefan, Weichert, Wilko, Brors, Benedikt, Schlesner, Matthias, Ball, Claudia R., Glimm, Hanno
Publicado no J Exp Med (2017)

Whole genome sequencing puts forward hypotheses on metastasis evolution and therapy in colorectal cancer

Por Ishaque, Naveed, Abba, Mohammed L., Hauser, Christine, Patil, Nitin, Paramasivam, Nagarajan, Huebschmann, Daniel, Leupold, Jörg Hendrik, Balasubramanian, Gnana Prakash, Kleinheinz, Kortine, Toprak, Umut H., Hutter, Barbara, Benner, Axel, Shavinskaya, Anna, Zhou, Chan, Gu, Zuguang, Kerssemakers, Jules, Marx, Alexander, Moniuszko, Marcin, Kozlowski, Miroslaw, Reszec, Joanna, Niklinski, Jacek, Eils, Jürgen, Schlesner, Matthias, Eils, Roland, Brors, Benedikt, Allgayer, Heike
Publicado no Nat Commun (2018)