Splice Variants of NaV1.7 Sodium Channels Have Distinct β Subunit-Dependent Biophysical Properties

by Farmer, Clare, Cox, James J., Fletcher, E. V., Woods, C. Geoffrey, Wood, John N., Schorge, Stephanie
Published 2012

Case Report: Neuropathic pain in a patient with congenital insensitivity to pain

by Wheeler, Daniel W., Lee, Michael C.H., Harrison, E. Katherine, Menon, David K., Woods, C. Geoffrey
Published 2015

Homozygosity for a missense mutation in the 67 kDa isoform of glutamate decarboxylase in a family with autosomal recessive spastic cerebral palsy: parallels with Stiff-Person Syndr...

by Lynex, Clare N, Carr, Ian M, Leek, Jack P, Achuthan, Rajgopal, Mitchell, Simon, Maher, Eamonn R, Woods, C Geoffrey, Bonthon, David T, Markham, Alex F
Published 2004

A Primary Microcephaly Protein Complex forms a ring around parental centrioles

by Sir, Joo-Hee, Barr, Alexis R., Nicholas, Adeline K., Carvalho, Ofelia P., Khurshid, Maryam, Sossick, Alex, Reichelt, Stefanie, D’Santos, Clive, Woods, C. Geoffrey, Gergely, Fanni
Published 2011

CCDC88A mutations cause PEHO-like syndrome in humans and mouse

by Nahorski, Michael S., Asai, Masato, Wakeling, Emma, Parker, Alasdair, Asai, Naoya, Canham, Natalie, Holder, Susan E., Chen, Ya-Chun, Dyer, Joshua, Brady, Angela F., Takahashi, Masahide, Woods, C. Geoffrey
Published 2016

A CEP215–HSET complex links centrosomes with spindle poles and drives centrosome clustering in cancer

by Chavali, Pavithra L., Chandrasekaran, Gayathri, Barr, Alexis R., Tátrai, Péter, Taylor, Chris, Papachristou, Evaggelia K., Woods, C. Geoffrey, Chavali, Sreenivas, Gergely, Fanni
Published 2016

Accelerated Evolution of the ASPM Gene Controlling Brain Size Begins Prior to Human Brain Expansion

by Kouprina, Natalay, Pavlicek, Adam, Mochida, Ganeshwaran H, Solomon, Gregory, Gersch, William, Yoon, Young-Ho, Collura, Randall, Ruvolo, Maryellen, Barrett, J. Carl, Woods, C. Geoffrey, Walsh, Christopher A, Jurka, Jerzy, Larionov, Vladimir
Published 2004

A novel disorder reveals clathrin heavy chain-22 is essential for human pain and touch development

by Nahorski, Michael S., Al-Gazali, Lihadh, Hertecant, Jozef, Owen, David J., Borner, Georg H. H., Chen, Ya-Chun, Benn, Caroline L., Carvalho, Ofélia P., Shaikh, Samiha S., Phelan, Anne, Robinson, Margaret S., Royle, Stephen J., Woods, C. Geoffrey
Published 2015

Regulation of Nav1.7: A Conserved SCN9A Natural Antisense Transcript Expressed in Dorsal Root Ganglia

by Koenig, Jennifer, Werdehausen, Robert, Linley, John E., Habib, Abdella M., Vernon, Jeffrey, Lolignier, Stephane, Eijkelkamp, Niels, Zhao, Jing, Okorokov, Andrei L., Woods, C. Geoffrey, Wood, John N., Cox, James J.
Published 2015

A Gain-of-Function Mutation in TRPA1 Causes Familial Episodic Pain Syndrome

by Kremeyer, Barbara, Lopera, Francisco, Cox, James J., Momin, Aliakmal, Rugiero, Francois, Marsh, Steve, Woods, C. Geoffrey, Jones, Nicholas G., Paterson, Kathryn J., Fricker, Florence R., Villegas, Andrés, Acosta, Natalia, Pineda-Trujillo, Nicolás G., Ramírez, Juan Diego, Zea, Julián, Burley, Mari-Wyn, Bedoya, Gabriel, Bennett, David L.H., Wood, John N., Ruiz-Linares, Andrés
Published 2010

Extreme Growth Failure is a Common Presentation of Ligase IV Deficiency

by Murray, Jennie E, Bicknell, Louise S, Yigit, Gökhan, Duker, Angela L, van Kogelenberg, Margriet, Haghayegh, Sara, Wieczorek, Dagmar, Kayserili, Hülya, Albert, Michael H, Wise, Carol A, Brandon, January, Kleefstra, Tjitske, Warris, Adilia, van der Flier, Michiel, Bamforth, J Steven, Doonanco, Kurston, Adès, Lesley, Ma, Alan, Field, Michael, Johnson, Diana, Shackley, Fiona, Firth, Helen, Woods, C Geoffrey, Nürnberg, Peter, Gatti, Richard A, Hurles, Matthew, Bober, Michael B, Wollnik, Bernd, Jackson, Andrew P
Published 2014