Genetic Variants in the Complement System Predisposing to Age-Related Macular Degeneration: A Review

av Schramm, Elizabeth C., Clark, Simon J., Triebwasser, Michael P., Raychaudhuri, Soumya, Seddon, Johanna, Atkinson, John P.
Publicerad 2014

Timing and mechanism of conceptus demise in a complement regulatory membrane protein deficient mouse

av Triebwasser, Michael P., Wu, Xiaobo, Bertram, Paula, Hourcade, Dennis E., Nelson, Donald Michael, Atkinson, John P.
I publikationen Am J Reprod Immunol (2018)

Complement Regulatory Protein CD46 Protects against Choroidal Neovascularization in Mice

av Lyzogubov, Valeriy, Wu, Xiaobo, Jha, Purushottam, Tytarenko, Ruslana, Triebwasser, Michael, Kolar, Grant, Bertram, Paula, Bora, Puran S., Atkinson, John P., Bora, Nalini S.
Publicerad 2014

Mapping rare, deleterious mutations in Factor H: Association with early onset, drusen burden, and lower antigenic levels in familial AMD

av Wagner, Erin K., Raychaudhuri, Soumya, Villalonga, Mercedes B., Java, Anuja, Triebwasser, Michael P., Daly, Mark J., Atkinson, John P., Seddon, Johanna M.
I publikationen Sci Rep (2016)

Rare genetic variants in the CFI gene are associated with advanced age-related macular degeneration and commonly result in reduced serum factor I levels

av Kavanagh, David, Yu, Yi, Schramm, Elizabeth C., Triebwasser, Michael, Wagner, Erin K., Raychaudhuri, Soumya, Daly, Mark J., Atkinson, John P., Seddon, Johanna M.
I publikationen Hum Mol Genet (2015)

Rare Variants in the Functional Domains of Complement Factor H Are Associated With Age-Related Macular Degeneration

av Triebwasser, Michael P., Roberson, Elisha D. O., Yu, Yi, Schramm, Elizabeth C., Wagner, Erin K., Raychaudhuri, Soumya, Seddon, Johanna M., Atkinson, John P.
I publikationen Invest Ophthalmol Vis Sci (2015)

Mutations in Complement Regulatory Proteins Predispose to Preeclampsia: A Genetic Analysis of the PROMISSE Cohort

av Salmon, Jane E., Heuser, Cara, Triebwasser, Michael, Liszewski, M. Kathryn, Kavanagh, David, Roumenina, Lubka, Branch, D. Ware, Goodship, Tim, Fremeaux-Bacchi, Veronique, Atkinson, John P.
Publicerad 2011

Whole-exome sequencing identifies rare, functional CFH variants in families with macular degeneration

av Yu, Yi, Triebwasser, Michael P., Wong, Edwin K. S., Schramm, Elizabeth C., Thomas, Brett, Reynolds, Robyn, Mardis, Elaine R., Atkinson, John P., Daly, Mark, Raychaudhuri, Soumya, Kavanagh, David, Seddon, Johanna M.
Publicerad 2014

Rare variants in CFI, C3 and C9 are associated with high risk of advanced age-related macular degeneration

av Seddon, Johanna M., Yu, Yi, Miller, Elizabeth C., Reynolds, Robyn, Tan, Perciliz L., Gowrisankar, Sivakumar, Goldstein, Jacqueline I., Triebwasser, Michael, Anderson, Holly E., Zerbib, Jennyfer, Kavanagh, David, Souied, Eric, Katsanis, Nicholas, Daly, Mark J., Atkinson, John, Raychaudhuri, Soumya
Publicerad 2013

PROTECTIVE LOW FREQUENCY VARIANTS FOR PREECLAMPSIA IN THE FLT1 GENE IN THE FINNISH POPULATION

av Lokki, A. Inkeri, Daly, Emma, Triebwasser, Michael, Kurki, Mitja I., Roberson, Elisha D.O., Häppölä, Paavo, Auro, Kirsi, Perola, Markus, Heinonen, Seppo, Kajantie, Eero, Kere, Juha, Kivinen, Katja, Pouta, Anneli, Salmon, Jane E., Meri, Seppo, Daly, Mark, Atkinson, John P., Laivuori, Hannele
I publikationen Hypertension (2017)