Autonomic Neurology

Por Woods, C Geoffrey
Publicado no Eur J Hum Genet (2016)

A practical guide to human cancer genetics

Por Woods, C Geoffrey
Publicado no Clin Med (Lond) (2007)

Primary microcephaly: do all roads lead to Rome?

Por Thornton, Gemma K., Woods, C. Geoffrey
Publicado em 2009

Autosomal Recessive Primary Microcephaly (MCPH): A Review of Clinical, Molecular, and Evolutionary Findings

Por Woods, C. Geoffrey, Bond, Jacquelyn, Enard, Wolfgang
Publicado em 2005

Splice Variants of Na(V)1.7 Sodium Channels Have Distinct β Subunit-Dependent Biophysical Properties

Por Farmer, Clare, Cox, James J., Fletcher, E. V., Woods, C. Geoffrey, Wood, John N., Schorge, Stephanie
Publicado em 2012

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

Por Wheeler, Daniel W., Lee, Michael C.H., Harrison, E. Katherine, Menon, David K., Woods, C. Geoffrey
Publicado no F1000Res (2015)

A Fifth Locus for Primary Autosomal Recessive Microcephaly Maps to Chromosome 1q31

Por Pattison, Lisa, Crow, Yanick J., Deeble, V. Jayne, Jackson, Andrew P., Jafri, Hussain, Rashid, Yasmin, Roberts, Emma, Woods, C. Geoffrey
Publicado em 2000

Novel SCN9A Mutations Underlying Extreme Pain Phenotypes: Unexpected Electrophysiological and Clinical Phenotype Correlations

Por Emery, Edward C., Habib, Abdella M., Cox, James J., Nicholas, Adeline K., Gribble, Fiona M., Woods, C. Geoffrey, Reimann, Frank
Publicado no J Neurosci (2015)

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

Por Chavali, Pavithra L., Chandrasekaran, Gayathri, Barr, Alexis R., Tátrai, Péter, Taylor, Chris, Papachristou, Evaggelia K., Woods, C. Geoffrey, Chavali, Sreenivas, Gergely, Fanni
Publicado no Nat Commun (2016)

Germline Mutation in NLRP2 (NALP2) in a Familial Imprinting Disorder (Beckwith-Wiedemann Syndrome)

Por Meyer, Esther, Lim, Derek, Pasha, Shanaz, Tee, Louise J., Rahman, Fatimah, Yates, John R. W., Woods, C. Geoffrey, Reik, Wolf, Maher, Eamonn R.
Publicado em 2009

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...

Por 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
Publicado em 2004

A Third Novel Locus for Primary Autosomal Recessive Microcephaly Maps to Chromosome 9q34

Por Moynihan, Leanne, Jackson, Andrew P., Roberts, Emma, Karbani, Gulshan, Lewis, Ian, Corry, Peter, Turner, Gwen, Mueller, Robert F., Lench, Nicholas J., Woods, C. Geoffrey
Publicado em 2000

A novel NGF mutation clarifies the molecular mechanism and extends the phenotypic spectrum of the HSAN5 neuropathy

Por Carvalho, Ofélia P, Thornton, Gemma K, Hertecant, Joseph, Houlden, Henry, Nicholas, Adeline K, Cox, James J, Rielly, Mary, Al-Gazali, Lihadh, Woods, C Geoffrey
Publicado em 2010

A Primary Microcephaly Protein Complex forms a ring around parental centrioles

Por 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
Publicado em 2011

CCDC88A mutations cause PEHO-like syndrome in humans and mouse

Por 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
Publicado no Brain (2016)

Regulation of Na(v)1.7: A Conserved SCN9A Natural Antisense Transcript Expressed in Dorsal Root Ganglia

Por 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.
Publicado no PLoS One (2015)

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

Por 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
Publicado em 2004

Loss-of-function mutations in sodium channel Na(v)1.7 cause anosmia

Por Weiss, Jan, Pyrski, Martina, Jacobi, Eric, Bufe, Bernd, Willnecker, Vivienne, Schick, Bernhard, Zizzari, Philippe, Gossage, Samuel J., Greer, Charles A., Leinders-Zufall, Trese, Woods, C. Geoffrey, Wood, John N., Zufall, Frank
Publicado em 2011

Human ASPM participates in spindle organisation, spindle orientation and cytokinesis

Por Higgins, Julie, Midgley, Carol, Bergh, Anna-Maria, Bell, Sandra M, Askham, Jonathan M, Roberts, Emma, Binns, Ruth K, Sharif, Saghira M, Bennett, Christopher, Glover, David M, Woods, C Geoffrey, Morrison, Ewan E, Bond, Jacquelyn
Publicado em 2010

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

Por 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
Publicado no Brain (2015)