Andrew E Fry

ORCID

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 9

Top Venues

Practical neurology

European journal of human genetics : EJHG

Nature reviews. Neurology

Brain sciences

This page only lists publications with an associated author ORCID identifier.

Publications

William Owen Pickrell, Andrew E Fry
Epilepsy genetics: a practical guide for adult neurologists. Practical neurology 23 (2) (2023)
William Owen Pickrell, Andrew E Fry
Epilepsy genetics: a practical guide for adult neurologists. Practical neurology 23 (2) (2023)
Vani Jain, Seow Hoong Foo, Stephen Chooi, Celia Moss, Richard Goodwin, Siren Berland, Angus John Clarke, Sally J Davies, Sian Corrin, Oliver Murch, Samantha Doyle, Gail E Graham, Lynn Greenhalgh, Susan E Holder, Diana Johnson, Ajith Kumar, Roger L Ladda, Susan Sell, Amber Begtrup, Sally A Lynch, Emma McCann, Rune Østern, Caroline Pottinger, Miranda Splitt, Andrew E Fry
Börjeson-Forssman-Lehmann syndrome: delineating the clinical and allelic spectrum in 14 new families. European journal of human genetics : EJHG (2023)
William Owen Pickrell, Andrew E Fry
Epilepsy genetics: a practical guide for adult neurologists. Practical neurology (2023)
Meena Balasubramanian, Alexander J M Dingemans, Shadi Albaba, Ruth Richardson, Thabo M Yates, Helen Cox, Sofia Douzgou, Ruth Armstrong, Francis H Sansbury, Katherine B Burke, Andrew E Fry, Nicola Ragge, Saba Sharif, Alison Foster, Annachiara De Sandre-Giovannoli, Sahar Elouej, Pradeep Vasudevan, Sahar Mansour, Kate Wilson, Helen Stewart, Solveig Heide, Caroline Nava, Boris Keren, Serwet Demirdas, Alice S Brooks, Marie Vincent, Bertrand Isidor, Sébastien Küry, Meyke Schouten, Erika Leenders, Wendy K Chung, Arie van Haeringen, Thomas Scheffner, Francois-Guillaume Debray, Susan M White, Maria Irene Valenzuela Palafoll, Rolph Pfundt, Ruth Newbury-Ecob, Tjitske Kleefstra
Comprehensive study of 28 individuals with SIN3A-related disorder underscoring the associated mild cognitive and distinctive facial phenotype. European journal of human genetics : EJHG 29 (4) (2021)
Oliver Murch, Vani Jain, Andreas Benneche, Kay Metcalfe, Emma Hobson, Katrina Prescott, Kate Chandler, Neeti Ghali, Jenny Carmichael, Nicola C Foulds, Julie Paulsen, Marie F Smeland, Siren Berland, Andrew E Fry
Further delineation of the clinical spectrum of White-Sutton syndrome: 12 new individuals and a review of the literature. European journal of human genetics : EJHG (2021)
Vassilis Ragoussis, Alistair T Pagnamenta, Rebecca L Haines, Edoardo Giacopuzzi, Martin A McClatchey, Julian R Sampson, Mohnish Suri, Alice Gardham, Jan-Maarten Cobben, Deborah Osio, Andrew E Fry, null null, Jenny C Taylor
Using data from the 100,000 Genomes Project to resolve conflicting interpretations of a recurrent TUBB2A mutation. Journal of medical genetics (2021)
Renske Oegema, Tahsin Stefan Barakat, Martina Wilke, Katrien Stouffs, Dina Amrom, Eleonora Aronica, Nadia Bahi-Buisson, Valerio Conti, Andrew E Fry, Tobias Geis, David Gomez Andres, Elena Parrini, Ivana Pogledic, Edith Said, Doriette Soler, Luis M Valor, Maha Saad Zaki, Ghayda M Mirzaa, William B Dobyns, Orly Reiner, Renzo Guerrini, Daniela T Pilz, Ute Hehr, Richard J Leventer, Anna C Jansen, Grazia M S Mancini, Nataliya Di Donato
International consensus recommendations on the diagnostic work-up for malformations of cortical development. Nature reviews. Neurology 16 (11) (2020)
Jennifer F Gardner, Thomas David Cushion, Georgios Niotakis, Heather E Olson, P Ellen Grant, Richard H Scott, Neil Stoodley, Julie S Cohen, Sakkubai Naidu, Tania Attie-Bitach, Maryse Bonnières, Lucile Boutaud, Férechté Encha-Razavi, Sheila M Palmer-Smith, Hood Mugalaasi, Jonathan G L Mullins, Daniela T Pilz, Andrew E Fry
Clinical and Functional Characterization of the Recurrent TUBA1A p.(Arg2His) Mutation. Brain sciences 8 (8) (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

Andrew E Fry