John Rogers

The challenge of developmentally appropriate care: predictive genetic testing in young people for familial adenomatous polyposis

Rony E Duncan, Lynn Gillam, Julian Savulescu, Robert Williamson, John G Rogers, Martin B Delatycki

Journal article  |  2010  |  FAMILIAL CANCER

Predictive genetic tests for familial adenomatous polyposis (FAP) are routinely offered to young people during early adolescence. ..

Reply to Richards: "Predictive genetic testing of adolescents for Huntington disease: A question of autonomy and harm"

Rony E Duncan, Lynn Gillam, Julian Savulescu, Robert Williamson, John G Rogers, Martin B Delatycki

Journal article  |  2008  |  AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Response to "Mutations of the NOGGIN and of the activin A type I receptor genes in fibrodysplasia ossificans progressiva (FOP)" by Lucotte et al.

FS Kaplan, M Xu, G Feldman, M Brown, T-J Cho, IH Choi, JM Connor, P Longo Ribeiro Delai, AN Economides, DL Glaser, J Groppe, T Katagiri, M Le Merrer, R Morhart, R Ravazzolo, JG Rogers, R Smith, JT Triffitt, JA Urtizberea, M Zasloff, et al.

Journal article  |  2008  |  Genet Couns

Erratum: A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva (Nature Genetics (2006) 38, (525-527))

EM Shore, M Xu, GJ Feldman, DA Fenstermacher, TJ Cho, IH Choi, JM Connor, P Delai, DL Glaser, M LeMerrer, R Morhart, JG Rogers, R Smith, JT Triffitt, JA Urtizberea, M Zasloff, MA Brown, FS Kaplan

Journal article  |  2007  |  Nature Genetics

FBN1, TGFBR1, and the Marfan-craniosynostosis/mental retardation disorders revisited

LC Ades, K Sullivan, A Biggin, EA Haan, M Brett, KJ Holman, J Dixon, S Robertson, AD Holmes, J Rogers, B Bennetts

Journal article  |  2006  |  AMERICAN JOURNAL OF MEDICAL GENETICS PART A

The recent identification of TGFBR2 mutations in Marfan syndrome II (MFSII) [Mizuguchi et al. (2004); Nat Genet 36:855-860] and of..

A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva.

Eileen M Shore, Meiqi Xu, George J Feldman, David A Fenstermacher, Tae-Joon Cho, In Ho Choi, J Michael Connor, Patricia Delai, David L Glaser, Martine LeMerrer, Rolf Morhart, John G Rogers, Roger Smith, James T Triffitt, J Andoni Urtizberea, Michael Zasloff, Matthew A Brown, Frederick S Kaplan

Journal article  |  2006  |  Nat Genet

Fibrodysplasia ossificans progressiva (FOP) is a rare autosomal dominant disorder of skeletal malformations and progressive extras..

What should we say?

J Savulescu, B Foddy, J Rogers

Journal article  |  2006  |  JOURNAL OF MEDICAL ETHICS

Abstract ethics mostly focuses on what we do. One form of action is a speech act. What we say can have profound effects. We can an..

The phenotype of fibrodysplasia ossificans progressiva

FS Kaplan, DL Glaser, EM Shore, GK Deirmengian, R Gupta, P Delai, R Morhart, R Smith, M Le Merrer, JG Rogers, JM Connor, JA Kitterman

Journal article  |  2005  |  Clinical Reviews in Bone and Mineral Metabolism

The phenotype of fibrodysplasia ossificans progressiva (FOP) includes two defining features: congenital malformation of the great ..

Longterm Follow-Up in Chondrodysplasia Punctata, Tibia-Metacarpal Type, Demonstrating Natural History

R Savarirayan, RJ Boyle, J Masel, JG Rogers, LJ Sheffield

Journal article  |  2004  |  American Journal of Medical Genetics

Longterm follow-up in chondrodysplasia punctata, tibia-metacarpal type, demonstrating natural history

R Savarirayan, RJ Boyle, J Masel, JG Rogers, LJ Sheffield

Journal article  |  2004  |  AMERICAN JOURNAL OF MEDICAL GENETICS PART A

We report the longterm clinical and radiological progression in three unrelated patients with the tibia-metacarpal form of chondro..