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Author/Creator Webster, Andrew R.

1. A genetic and clinical study of individuals with nonsyndromic retinopathy consequent upon sequence variants in HGSNAT, the gene associated with Sanfilippo C mucopolysaccharidosis. Issue 3 (7th August 2020)

Authors:
Schiff, Elena R.; Daich Varela, Malena; Robson, Anthony G.; Pierpoint, Karen; Ba‐Abbad, Rola; Nutan, Savita; Zein, Wadih M.; Ullah, Ehsan; Huryn, Laryssa A.; Tuupanen, Sari; Mahroo, Omar A.; Michaelides, Michel; Burke, Derek; Harvey, Katie; Arno, Gavin; Hufnagel, Robert B.; Webster, Andrew R.
Other Names:
Hufnagel Robert guestEditor.; Walter Michael guestEditor.; Arno Gavin guestEditor.
Journal:
American journal of medical genetics
Issue:
Volume 184:Issue 3(2020)
Page Start:
631
Record Type:
Journal Article
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2. A Homozygous Mutation in the TUB Gene Associated with Retinal Dystrophy and Obesity. Issue 3 (20th December 2013)

Authors:
Borman, Arundhati Dev; Pearce, Laura R.; Mackay, Donna S.; Nagel‐Wolfrum, Kerstin; Davidson, Alice E.; Henderson, Robert; Garg, Sumedha; Waseem, Naushin H.; Webster, Andrew R.; Plagnol, Vincent; Wolfrum, Uwe; Farooqi, I. Sadaf; Moore, Anthony T.
Journal:
Human mutation
Issue:
Volume 35:Issue 3(2014:Mar.)
Page Start:
289
Record Type:
Journal Article
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4. AN ASSOCIATION BETWEEN STELLATE NONHEREDITARY IDIOPATHIC FOVEOMACULAR RETINOSCHISIS, PERIPHERAL RETINOSCHISIS, AND POSTERIOR HYALOID ATTACHMENT. Issue 11 (November 2021)

Authors:
Bloch, Edward; Flores-Sánchez, Blanca; Georgiadis, Odysseas; Sundaram, Venki; Saihan, Zubin; Mahroo, Omar A.; Webster, Andrew R.; da Cruz, Lyndon
Journal:
Retina
Issue:
Volume 41:Issue 11(2021)
Page Start:
Record Type:
Journal Article
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6. CNGB1‐related rod‐cone dystrophy: A mutation review and update. Issue 6 (16th May 2021)

Authors:
Nassisi, Marco; Smirnov, Vasily M.; Solis Hernandez, Cyntia; Mohand‐Saïd, Saddek; Condroyer, Christel; Antonio, Aline; Kühlewein, Laura; Kempf, Melanie; Kohl, Susanne; Wissinger, Bernd; Nasser, Fadi; Ragi, Sara D.; Wang, Nan‐Kai; Sparrow, Janet R.; Greenstein, Vivienne C.; Michalakis, Stylianos; ...
Journal:
Human mutation
Issue:
Volume 42:Issue 6(2021)
Page Start:
641
Record Type:
Journal Article
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7. Cover, Volume 42, Issue 2. Issue 2 (25th January 2021)

Authors:
Poulter, James A.; Gravett, Molly S. C.; Taylor, Rachel L.; Fujinami, Kaoru; De Zaeytijd, Julie; Bellingham, James; Rehman, Atta Ur; Hayashi, Takaaki; Kondo, Mineo; Rehman, Abdur; Ansar, Muhammad; Donnelly, Dan; Toomes, Carmel; Ali, Manir; De Baere, Elfride; Leroy, Bart P.; Davies, Nigel P.; Hend...
Journal:
Human mutation
Issue:
Volume 42:Issue 2(2021)
Page Start:
ii
Record Type:
Journal Article
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8. Delineating the expanding phenotype associated with SCAPER gene mutation. Issue 8 (13th June 2019)

Authors:
Fasham, James; Arno, Gavin; Lin, Siying; Xu, Mingchu; Carss, Keren J.; Hull, Sarah; Lane, Amelia; Robson, Anthony G.; Wenger, Olivia; Self, Jay E.; Harlalka, Gaurav V.; Salter, Claire G.; Schema, Lynn; Moss, Timothy J.; Cheetham, Michael E.; Moore, Anthony T.; Raymond, F. Lucy; Chen, Rui; Baple, ...
Journal:
American journal of medical genetics
Issue:
Volume 179:Issue 8(2019)
Page Start:
1665
Record Type:
Journal Article
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