Flies without Centrioles von Basto, Renata, Lau, Joyce, Vinogradova, Tatiana, Gardiol, Alejandra, Woods, C. Geoffrey, Khodjakov, Alexey, Raff, Jordan W.

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New Mendelian Disorders of Painlessness von Nahorski, Michael S, Chen, Ya-Chun, Woods, C. Geoffrey

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An SCN9A channelopathy causes congenital inability to experience pain von Reimann, Frank, McHale, Duncan P, Valente, Enza Maria, Jafri, Hussain, Al-Gazali, Lihadh, Gribble, Fiona M, Thornton, Gemma, Gorman, Shaun, Williams, Richard, Wood, John N, Nicholas, Adeline K, Roberts, Emma, Mannan, Jovaria, Springell, Kelly, Woods, C. Geoffrey, Cox, James J, Raashid, Yasmin, Karbani, Gulshan, Hamamy, Henan

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

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Pain perception is altered by a nucleotide polymorphism in SCN9A von Reimann, Frank, Cox, James J, Belfer, Inna, Diatchenko, Luda, Zaykin, Dmitri V, McHale, Duncan P, Drenth, Joost P.H, Dai, Feng, Wheeler, Jerry, Sanders, Frances, Wood, Linda, Wu, Tian-Xia, Karppinen, Jaro, Nikolajsen, Lone, Männikkö, Minna, Max, Mitchell B, Kiselycznyk, Carly, Poddar, Minakshi, te Morsche, Rene H.M, Smith, Shad, Gibson, Dustin, Kelempisioti, Anthi, Maixner, William, Gribble, Fiona M, Woods, C. Geoffrey

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Germline mutation in NLRP2 (NALP2) in a familial imprinting disorder (Beckwith-Wiedemann Syndrome) von Meyer, Esther, Lim, Derek, Pasha, Shanaz, Tee, Louise J, Rahman, Fatimah, Yates, John R W, Woods, C Geoffrey, Reik, Wolf, Maher, Eamonn R

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Mutations in the Cilia Gene ARL13B Lead to the Classical Form of Joubert Syndrome von Cantagrel, Vincent, Silhavy, Jennifer L., Bielas, Stephanie L., Swistun, Dominika, Marsh, Sarah E., Bertrand, Julien Y., Audollent, Sophie, Attié-Bitach, Tania, Holden, Kenton R., Dobyns, William B., Traver, David, Al-Gazali, Lihadh, Ali, Bassam R., Lindner, Tom H., Caspary, Tamara, Otto, Edgar A., Hildebrandt, Friedhelm, Glass, Ian A., Logan, Clare V., Johnson, Colin A., Bennett, Christopher, Brancati, Francesco, Valente, Enza Maria, Woods, C. Geoffrey, Gleeson, Joseph G.

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Mutations in linker for activation of T cells (LAT) lead to a novel form of severe combined immunodeficiency von Bacchelli, Chiara, PhD, Moretti, Federico A., PhD, Carmo, Marlene, PhD, Adams, Stuart, PhD, Stanescu, Horia C., PhD, Pearce, Kerra, PhD, Madkaikar, Manisha, MD, PhD, Gilmour, Kimberly C., PhD, Nicholas, Adeline K., PhD, Woods, C. Geoffrey, MD, PhD, Kleta, Robert, MD, PhD, Beales, Phil L., MD, PhD, Qasim, Waseem, MD, PhD, Gaspar, H. Bobby, MD, PhD

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The Essential Role of Centrosomal NDE1 in Human Cerebral Cortex Neurogenesis von Bakircioglu, Mehmet, Carvalho, Ofélia P., Khurshid, Maryam, Cox, James J., Tuysuz, Beyhan, Barak, Tanyeri, Yilmaz, Saliha, Caglayan, Okay, Dincer, Alp, Nicholas, Adeline K., Quarrell, Oliver, Springell, Kelly, Karbani, Gulshan, Malik, Saghira, Gannon, Caroline, Sheridan, Eamonn, Crosier, Moira, Lisgo, Steve N., Lindsay, Susan, Bilguvar, Kaya, Gergely, Fanni, Gunel, Murat, Woods, C. Geoffrey

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ASPM is a major determinant of cerebral cortical size von Woods, C. Geoffrey, Bond, Jacquelyn, Roberts, Emma, Mochida, Ganesh H, Hampshire, Daniel J, Scott, Sheila, Askham, Jonathan M, Springell, Kelly, Mahadevan, Meera, Crow, Yanick J, Markham, Alexander F, Walsh, Christopher A

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Evolutionarily Assembled cis-Regulatory Module at a Human Ciliopathy Locus von JEONG HO LEE, SILHAVY, Jennifer L, GABRIEL, Stacey B, RUSS, Carsten, LOGAN, Clare V, MALIK SHARIF, Saghira, BENNETT, Christopher P, ABE, Masumi, HILDEBRANDT, Friedhelm, DIPLAS, Bill H, ATTIE-BITACH, Tania, KATSANIS, Nicholas, JI EUN LEE, RAJAB, Anna, KOUL, Roshan, SZTRIHA, Laszlo, WATERS, Elizabeth R, FERRO-NOVICK, Susan, GEOFFREY WOODS, C, JOHNSON, Colin A, MARIA VALENCE, Enza, ZAKI, Maha S, GLEESON, Joseph G, AL-GAZALI, Lihadh, THOMAS, Sophie, DAVIS, Erica E, BIELAS, Stephanie L, HILL, Kiley J, LANNICELLI, Miriam, BRANCATI, Francesco

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Accelerated evolution of the ASPM gene controlling brain size begins prior to human brain expansion von 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

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Distinguishing the four genetic causes of jouberts syndrome-related disorders von Valente, Enza Maria, Marsh, Sarah E., Castori, Marco, Dixon-Salazar, Tracy, Bertini, Enrico, Al-Gazali, Lihadh, Messer, Jean, Barbot, Clara, Woods, C. Geoffrey, Boltshauser, Eugen, Al-Tawari, Asma A., Salpietro, Carmelo D., Kayserili, Hulya, Sztriha, László, Gribaa, Moez, Koenig, Michel, Dallapiccola, Bruno, Gleeson, Joseph G.

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Loss-of-function mutations in sodium channel Na sub(v)1.7 cause anosmia von Weiss, Jan, Pyrski, Martina, Jacobi, Eric, Bufe, Bernd, Willnecker, Vivienne, Schick, Bernhard, Zizzari, Philippe, Gossage, Samuel J, Greer, Charles A, Leinders-Zufall, Trese, Woods, CGeoffrey, Wood, John N, Zufall, Frank

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Crossing the Midline von Woods, C. Geoffrey

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