Zobrazeno 1 - 10
of 121
pro vyhledávání: '"Petri S, Mattila"'
Autor:
Mahmood F. Bhutta, Jane Lambie, Lindsey Hobson, Anuj Goel, Lena Hafrén, Elisabet Einarsdottir, Petri S. Mattila, Martin Farrall, Steve Brown, Martin J. Burton
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-7 (2017)
Abstract Chronic otitis media with effusion (COME) is the most common cause of hearing loss in children, and known to have high heritability. Mutant mouse models have identified Fbxo11, Evi1, Tgif1, and Nisch as potential risk loci. We recruited chil
Externí odkaz:
https://doaj.org/article/4e3ad4f89c544c7ca34f1dfdf0d95724
Autor:
Charles E. Robertson, Alessandra Nadine E. Chiong, Michèle M. Sale, Nanette R. Lee, Kimberly Mae C. Ong, Sairah Yousaf, Jose Pedrito M. Magno, Diana Ir, Patrick John Labra, Petri S. Mattila, Maria Luz San Agustin, Generoso T. Abes, Erasmo Gonzalo D V Llanes, Ma. Carmina Espiritu-Chiong, Maria Rina T. Reyes-Quintos, Tori C. Bootpetch, Wasyl Szeremeta, Allen F. Ryan, Teresa Luisa G. Cruz, Arnaud P. J. Giese, Suzanne M. Leal, Rachelle Marie A. Nonato, Zubair M. Ahmed, Abner L. Chan, Karen L. Mohlke, Rhodieleen Anne R. de la Cruz, Regie Lyn P. Santos-Cortez, Matthew J. Steritz, Tasnee Chonmaitree, Daniel N. Frank, Eva Maria Cutiongco-de la Paz, Melquiadesa Pedro, Elisabet Einarsdottir, Talitha Karisse L. Yarza, Juha Kere, Deborah A. Nickerson, Lena Hafrén, Niaz Ahankoob, Michael J. Bamshad, Kathleen Daly, Ma. Leah C. Tantoco, Charlotte M. Chiong, Harold S. Pine, Saima Riazuddin
Publikováno v:
Journal of Medical Genetics. 58:442-452
BackgroundOtitis media (OM) susceptibility has significant heritability; however, the role of rare variants in OM is mostly unknown. Our goal is to identify novel rare variants that confer OM susceptibility.MethodsWe performed exome and Sanger sequen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4c1f3273286a54b911b866b3c1c6e874
https://doi.org/10.1136/jmedgenet-2020-106844
https://doi.org/10.1136/jmedgenet-2020-106844
Autor:
Lena Hafrén, Elisabet Einarsdottir, Erna Kentala, Sari Hammarén-Malmi, Mahmood F Bhutta, Carol J MacArthur, Beth Wilmot, Margaretha Casselbrant, Yvette P Conley, Daniel E Weeks, Ellen M Mandel, Outi Vaarala, Anna Kallio, Merit Melin, Janne K Nieminen, Eira Leinonen, Juha Kere, Petri S Mattila
Publikováno v:
PLoS ONE, Vol 10, Iss 7, p e0132551 (2015)
Predisposition to childhood otitis media (OM) has a strong genetic component, with polymorphisms in innate immunity genes suspected to contribute to risk. Studies on several genes have been conducted, but most associations have failed to replicate in
Externí odkaz:
https://doaj.org/article/25a3ab538da14180bfb286e67f411501
Autor:
Tori C. Bootpetch, Todd Wine, Melissa A. Scholes, Patricia J. Yoon, Michael J. Bamshad, Sven-Olrik Streubel, Daniel N. Frank, Stephen P. Cass, Harold S. Pine, Tasnee Chonmaitree, Michèle M. Sale, Herman A. Jenkins, Ayesha Yousaf, Elisabet Einarsdottir, Erin E. Baschal, Ani Manichaikul, Juha Kere, Kenny H. Chan, Petri S. Mattila, Christina L Elling, Jeremy D. Prager, Regie Lyn P. Santos-Cortez, Lena Hafrén, Norman R. Friedman, Wasyl Szeremeta, Eric D. Larson, Saima Riazuddin, Allen F. Ryan, Rehan S. Shaikh, Rafaqat Ishaq, Suzanne M. Leal, Deborah A. Nickerson, Kathleen Daly, Samuel P. Gubbels, Zubair M. Ahmed
Publikováno v:
Scientific Reports
Scientific Reports, Vol 10, Iss 1, Pp 1-12 (2020)
Scientific Reports, Vol 10, Iss 1, Pp 1-12 (2020)
Otitis media (OM), a very common disease in young children, can result in hearing loss. In order to potentially replicate previously reported associations between OM and PLG, exome and Sanger sequencing, RNA-sequencing of saliva and middle ear sample
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29baf8c7c7adbb1c2ce8a28870aa6d39
http://hdl.handle.net/10138/320494
http://hdl.handle.net/10138/320494
Autor:
Jaana Hagström, Lauri Jouhi, Antti Mäkitie, Petri S. Mattila, Caj Haglund, Timo Carpén, Stina Syrjänen, Reija Randén-Brady
Publikováno v:
Cancer Immunology, Immunotherapy
Background The etiological role of human papillomavirus (HPV) in oropharyngeal squamous cell carcinoma (OPSCC) is confirmed. However, the role of other oncoviruses in OPSCC is unknown. Materials and methods A total of 158 consecutive OPSCC patients t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac1acf81bc1da7c2c076fa7da2f6b2f3
http://hdl.handle.net/10138/318893
http://hdl.handle.net/10138/318893
Autor:
Daniel N, Frank, Arnaud P J, Giese, Lena, Hafren, Tori C, Bootpetch, Talitha Karisse L, Yarza, Matthew J, Steritz, Melquiadesa, Pedro, Patrick John, Labra, Kathleen A, Daly, Ma Leah C, Tantoco, Wasyl, Szeremeta, Maria Rina T, Reyes-Quintos, Niaz, Ahankoob, Erasmo Gonzalo D V, Llanes, Harold S, Pine, Sairah, Yousaf, Diana, Ir, Elisabet, Einarsdottir, Rhodieleen Anne R, de la Cruz, Nanette R, Lee, Rachelle Marie A, Nonato, Charles E, Robertson, Kimberly Mae C, Ong, Jose Pedrito M, Magno, Alessandra Nadine E, Chiong, Ma Carmina, Espiritu-Chiong, Maria Luz, San Agustin, Teresa Luisa G, Cruz, Generoso T, Abes, Michael J, Bamshad, Eva Maria, Cutiongco-de la Paz, Juha, Kere, Deborah A, Nickerson, Karen L, Mohlke, Saima, Riazuddin, Abner, Chan, Petri S, Mattila, Suzanne M, Leal, Allen F, Ryan, Zubair M, Ahmed, Tasnee, Chonmaitree, Michele M, Sale, Charlotte M, Chiong, Regie Lyn P, Santos-Cortez
Publikováno v:
J Med Genet
BACKGROUND: Otitis media (OM) susceptibility has significant heritability, however the role of rare variants in OM is mostly unknown. Our goal is to identify novel rare variants that confer OM susceptibility. METHODS: We performed exome and Sanger se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b44b2d0faca9516c60eb8a0c6d7e44ef
https://pubmed.ncbi.nlm.nih.gov/32709676
https://pubmed.ncbi.nlm.nih.gov/32709676
Autor:
Amy Dickinson, Jaana Hagström, Petri S. Mattila, Tiialotta Tohmola, Sakari Joenväärä, Caj Haglund, Antti Mäkitie, Reija Randén-Brady, Mayank Saraswat, Timo Carpén, Suvi Silén, Robert Silén, Stina Syrjänen
Publikováno v:
PLoS ONE, Vol 15, Iss 6, p e0233974 (2020)
PLoS ONE
PLoS ONE
BackgroundThe surrogate immunohistochemical marker, p16INK4a, is used in clinical practice to determine the high-risk human papillomavirus (HPV) status of oropharyngeal squamous cell carcinomas (OPSCC). With a specificity of 83%, this will misclassif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85aa25359922be3c6a23f4841fc10f2a
https://doaj.org/article/3102e6c378c849ca9c6bfa6b280948e7
https://doaj.org/article/3102e6c378c849ca9c6bfa6b280948e7
Autor:
Tingting Chen, Lea Hedman, Petri S Mattila, Laura Jartti, Tuomas Jartti, Olli Ruuskanen, Maria Söderlund-Venermo, Klaus Hedman
Publikováno v:
PLoS ONE, Vol 7, Iss 8, p e42376 (2012)
Biotin is an essential vitamin that binds streptavidin or avidin with high affinity and specificity. As biotin is a small molecule that can be linked to proteins without affecting their biological activity, biotinylation is applied widely in biochemi
Externí odkaz:
https://doaj.org/article/cf1be3ccbaf341d9bdadcb965da39160
Autor:
Lena Hafrén, Regie Lyn P. Santos-Cortez, Petri S. Mattila, Elisabet Einarsdottir, Juha Kere, Brett M. Wiesen
Publikováno v:
Genet Test Mol Biomarkers
Aim: To determine if there is an association between ABO variants or blood types and otitis media. Methods: DNA samples from 214 probands from Finnish families with recurrent acute (RAOM) and/or chronic otitis media with effusion (COME) were submitte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19f444705fdd02b635020d1ccdef0e92
https://europepmc.org/articles/PMC6857544/
https://europepmc.org/articles/PMC6857544/
Autor:
Rachel Ann P Santos, Melquiadesa Pedro, Talitha Karisse L. Yarza, Charlotte M. Chiong, Janak A. Patel, Christopher Greenlee, Zubair M. Ahmed, Rose Anne Q Rosanes, Rehan S. Shaikh, Melissa A. Scholes, Matthew J. Steritz, Norman R. Friedman, Todd Wine, Abner L. Chan, Ma. Leah C. Tantoco, Patricia J. Yoon, Tori Bootpetch Roberts, Erasmo Gonzalo D V Llanes, Jeremy D. Prager, Anushree Acharya, Eric D. Larson, Karen L. Mohlke, Saima Riazuddin, Maria Rina T. Reyes-Quintos, Jose Pedrito M. Magno, Generoso T. Abes, Tasnee Chonmaitree, Petri S. Mattila, Teresa Luisa G. Cruz, Lena Hafrén, Elisabet Einarsdottir, Ayesha Yousaf, Catherine B. Anderson, Juha Kere, Jonathan Cardwell, Amanda G. Ruiz, Michael J. Bamshad, Herman A. Jenkins, Ivana V. Yang, Deborah A. Nickerson, Samuel P. Gubbels, Sven-Olrik Streubel, Suzanne M. Leal, Katerina Kechris, David A. Schwartz, Sheryl Mae Lagrana-Villagracia, Regie Lyn P. Santos-Cortez, Aileen Trinidad R Santos, Nanette R. Lee, Kenny H. Chan, Dylan Ray, Eva Maria Cutiongco-de la Paz, Stephen P. Cass
Publikováno v:
Hum Mutat
A genetic basis for otitis media is established, however, the role of rare variants in disease etiology is largely unknown. Previously a duplication variant within A2ML1 was identified as a significant risk factor for otitis media in an indigenous Fi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffa230c38770ef2c2a612a2e6653a5b4
http://hdl.handle.net/10138/312957
http://hdl.handle.net/10138/312957