Investigation into the Role of N‐Acetylaspartate in Cerebral Osmoregulation von Taylor, Deanna L., Davies, Siân E. C., Obrenovitch, Tihomir P., Doheny, Mary H., Patsalos, Philip N., Clark, John B., Symon, Lindsay

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A High-performance Liquid-chromatographic Microanalytical Procedure for the Rapid Estimation of Piracetam in Plasma or Cerebrospinal Fluid von DOHENY, M. H., O'CONNELL, M. T., PATSALOS, P. N.

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The effects of the?2-agonist drug clenbuterol on taurine levels in heart and other tissues in the rat von Doheny, M. H., Waterfield, C. J., Timbrell, John A.

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A microdialysis study of glycinamide, glycine and other amino acid neurotransmitters in rat frontal cortex and hippocampus after the administration of milacemide, a glycine pro-dru... von Doheny, M H, Nagaki, S, Patsalos, P N

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A comparison of the OPUS and TDx analysers for antiepileptic drug monitoring von O'CONNELL, M. T, NEVILLE RATNARAJ, ELYAS, A. A, DOHENY, M. H, DARSOT, S, PATSALOS, P. N

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The effects of the beta 2-agonist drug clenbuterol on taurine levels in heart and other tissues in the rat von Doheny, M H, Waterfield, C J, Timbrell, J A

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Genome-wide Association Scan for Childhood Caries Implicates Novel Genes von Shaffer, J.R., Wang, X., Feingold, E., Lee, M., Begum, F., Weeks, D.E., Cuenco, K.T., Barmada, M.M., Wendell, S.K., Crosslin, D.R., Laurie, C.C., Doheny, K.F., Pugh, E.W., Zhang, Q., Feenstra, B., Geller, F., Boyd, H.A., Zhang, H., Melbye, M., Murray, J.C., Weyant, R.J., Crout, R., McNeil, D.W., Levy, S.M., Slayton, R.L., Willing, M.C., Broffitt, B., Vieira, A.R., Marazita, M.L.

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A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4 von Beaty, Terri H, Murray, Jeffrey C, Marazita, Mary L, Munger, Ronald G, Ruczinski, Ingo, Hetmanski, Jacqueline B, Liang, Kung Yee, Wu, Tao, Murray, Tanda, Fallin, M Daniele, Redett, Richard A, Raymond, Gerald, Schwender, Holger, Jin, Sheng-Chih, Cooper, Margaret E, Dunnwald, Martine, Mansilla, Maria A, Leslie, Elizabeth, Bullard, Stephen, Lidral, Andrew C, Moreno, Lina M, Menezes, Renato, Vieira, Alexandre R, Petrin, Aline, Wilcox, Allen J, Lie, Rolv T, Jabs, Ethylin W, Wu-Chou, Yah Huei, Chen, Philip K, Wang, Hong, Ye, Xiaoqian, Huang, Shangzhi, Yeow, Vincent, Chong, Samuel S, Jee, Sun Ha, Shi, Bing, Christensen, Kaare, Melbye, Mads, Doheny, Kimberly F, Pugh, Elizabeth W, Ling, Hua, Castilla, Eduardo E, Czeizel, Andrew E, Ma, Lian, Field, L Leigh, Brody, Lawrence, Pangilinan, Faith, Mills, James L, Molloy, Anne M, Kirke, Peadar N, Scott, John M, Arcos-Burgos, Mauricio, Scott, Alan F

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Genomewide association study for susceptibility genes contributing to familial Parkinson disease von Pankratz, Nathan, Wilk, Jemma B, Latourelle, Jeanne C, DeStefano, Anita L, Halter, Cheryl, Pugh, Elizabeth W, Doheny, Kimberly F, Gusella, James F, Nichols, William C, Foroud, Tatiana, Myers, Richard H

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The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities von Chong, Jessica X., Buckingham, Kati J., Jhangiani, Shalini N., Boehm, Corinne, Sobreira, Nara, Smith, Joshua D., Harrell, Tanya M., McMillin, Margaret J., Wiszniewski, Wojciech, Gambin, Tomasz, Coban Akdemir, Zeynep H., Doheny, Kimberly, Scott, Alan F., Avramopoulos, Dimitri, Chakravarti, Aravinda, Hoover-Fong, Julie, Mathews, Debra, Witmer, P. Dane, Ling, Hua, Hetrick, Kurt, Watkins, Lee, Patterson, Karynne E., Reinier, Frederic, Blue, Elizabeth, Muzny, Donna, Kircher, Martin, Bilguvar, Kaya, López-Giráldez, Francesc, Sutton, V. Reid, Tabor, Holly K., Leal, Suzanne M., Gunel, Murat, Mane, Shrikant, Gibbs, Richard A., Boerwinkle, Eric, Hamosh, Ada, Shendure, Jay, Lupski, James R., Lifton, Richard P., Valle, David, Nickerson, Deborah A., Bamshad, Michael J.

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Truncating mutations in the last exon of NOTCH3 cause lateral meningocele syndrome von Gripp, Karen W., Robbins, Katherine M., Sobreira, Nara L., Witmer, P. Dane, Bird, Lynne M., Avela, Kristiina, Makitie, Outi, Alves, Daniela, Hogue, Jacob S., Zackai, Elaine H., Doheny, Kimberly F., Stabley, Deborah L., Sol-Church, Katia

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Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease von Payami, Haydeh, Hamza, Taye H, Zabetian, Cyrus P, Tenesa, Albert, Laederach, Alain, Montimurro, Jennifer, Yearout, Dora, Kay, Denise M, Doheny, Kimberly F, Paschall, Justin, Pugh, Elizabeth, Kusel, Victoria I, Collura, Randall, Roberts, John, Griffith, Alida, Samii, Ali, Scott, William K, Nutt, John, Factor, Stewart A

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Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma von Wiggs, Janey L, Yaspan, Brian L, Hauser, Michael A, Kang, Jae H, Allingham, R Rand, Olson, Lana M, Abdrabou, Wael, Fan, Bao J, Wang, Dan Y, Brodeur, Wendy, Budenz, Donald L, Caprioli, Joseph, Crenshaw, Andrew, Crooks, Kristy, Delbono, Elizabeth, Doheny, Kimberly F, Friedman, David S, Gaasterland, Douglas, Gaasterland, Terry, Laurie, Cathy, Lee, Richard K, Lichter, Paul R, Loomis, Stephanie, Liu, Yutao, Medeiros, Felipe A, McCarty, Cathy, Mirel, Daniel, Moroi, Sayoko E, Musch, David C, Realini, Anthony, Rozsa, Frank W, Schuman, Joel S, Scott, Kathleen, Singh, Kuldev, Stein, Joshua D, Trager, Edward H, Vanveldhuisen, Paul, Vollrath, Douglas, Wollstein, Gadi, Yoneyama, Sachiko, Zhang, Kang, Weinreb, Robert N, Ernst, Jason, Kellis, Manolis, Masuda, Tomohiro, Zack, Don, Richards, Julia E, Pericak-Vance, Margaret, Pasquale, Louis R, Haines, Jonathan L

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Meta-analysis of Parkinson's Disease: Identification of a novel locus, RIT2 von Pankratz, Nathan, Beecham, Gary W., DeStefano, Anita L., Dawson, Ted M., Doheny, Kimberly F., Factor, Stewart A., Hamza, Taye H., Hung, Albert Y., Hyman, Bradley T., Ivinson, Adrian J., Krainc, Dmitri, Latourelle, Jeanne C., Clark, Lorraine N., Marder, Karen, Martin, Eden R., Mayeux, Richard, Ross, Owen A., Scherzer, Clemens R., Simon, David K., Tanner, Caroline, Vance, Jeffery M., Wszolek, Zbigniew K., Zabetian, Cyrus P., Myers, Richard H., Payami, Haydeh, Scott, William K., Foroud, Tatiana

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Copy number variation in familial Parkinson disease von Pankratz, Nathan, Dumitriu, Alexandra, Hetrick, Kurt N, Sun, Mei, Latourelle, Jeanne C, Wilk, Jemma B, Halter, Cheryl, Doheny, Kimberly F, Gusella, James F, Nichols, William C, Myers, Richard H, Foroud, Tatiana, DeStefano, Anita L

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Genome‐Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry von Taylor, Kimberly E., Wong, Quenna, Levine, David M., McHugh, Caitlin, Laurie, Cathy, Doheny, Kimberly, Lam, Mi Y., Baer, Alan N., Challacombe, Stephen, Lanfranchi, Hector, Schiødt, Morten, Srinivasan, M., Umehara, Hisanori, Vivino, Frederick B., Zhao, Yan, Shiboski, Stephen C., Daniels, Troy E., Greenspan, John S., Shiboski, Caroline H., Criswell, Lindsey A.

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A genome-wide association study on African-ancestry populations for asthma von Mathias, Rasika A., ScD, Grant, Audrey V., PhD, Rafaels, Nicholas, MS, Hand, Tracey, MS, Gao, Li, MD, PhD, Vergara, Candelaria, MSc, Tsai, Yuhjung J., MD, Yang, Mao, MS, Campbell, Monica, BS, Foster, Cassandra, Gao, Peisong, MD, PhD, Togias, A., MD, Hansel, Nadia N., MD, MPH, Diette, Gregory, MD, Adkinson, N. Franklin, MD, Liu, Mark C., MD, Faruque, Mezbah, MD, PhD, Dunston, Georgia M., PhD, Watson, Harold R., MD, Bracken, Michael B., PhD, Hoh, Josephine, PhD, Maul, Pissamai, RN, Maul, Trevor, RN, Jedlicka, Anne E., MS, Murray, Tanda, MS, Hetmanski, Jacqueline B., MS, Ashworth, Roxann, MHS, Ongaco, Chrissie M., BS, Hetrick, Kurt N., MS, Doheny, Kimberly F., PhD, Pugh, Elizabeth W., PhD, MPH, Rotimi, Charles N., PhD, Ford, Jean, MD, Eng, Celeste, BS, Burchard, Esteban G., MD, Sleiman, Patrick M.A., PhD, Hakonarson, Hakon, MD, PhD, Forno, Erick, MD, Raby, Benjamin A., MD, Weiss, Scott T., MD, Scott, Alan F., PhD, Kabesch, Michael, MD, Liang, Liming, MS, Abecasis, Gonçalo, PhD, Moffatt, Miriam F., PhD, Cookson, William O.C., MD, Ruczinski, Ingo, PhD, Beaty, Terri H., PhD, Barnes, Kathleen C., PhD

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Detectable clonal mosaicism from birth to old age and its relationship to cancer von Laurie, Cathy C, Laurie, Cecelia A, Rice, Kenneth, Doheny, Kimberly F, Zelnick, Leila R, McHugh, Caitlin P, Ling, Hua, Hetrick, Kurt N, Pugh, Elizabeth W, Amos, Chris, Wei, Qingyi, Wang, Li-e, Lee, Jeffrey E, Barnes, Kathleen C, Hansel, Nadia N, Mathias, Rasika, Daley, Denise, Beaty, Terri H, Scott, Alan F, Ruczinski, Ingo, Scharpf, Rob B, Bierut, Laura J, Hartz, Sarah M, Landi, Maria Teresa, Freedman, Neal D, Goldin, Lynn R, Ginsburg, David, Li, Jun, Desch, Karl C, Strom, Sara S, Blot, William J, Signorello, Lisa B, Ingles, Sue A, Chanock, Stephen J, Berndt, Sonja I, Le Marchand, Loic, Henderson, Brian E, Monroe, Kristine R, Heit, John A, de Andrade, Mariza, Armasu, Sebastian M, Regnier, Cynthia, Lowe, William L, Hayes, M Geoffrey, Marazita, Mary L, Feingold, Eleanor, Murray, Jeffrey C, Melbye, Mads, Feenstra, Bjarke, Kang, Jae H, Wiggs, Janey L, Jarvik, Gail P, McDavid, Andrew N, Seshan, Venkatraman E, Mirel, Daniel B, Crenshaw, Andrew, Sharopova, Nataliya, Wise, Anastasia, Shen, Jess, Crosslin, David R, Levine, David M, Zheng, Xiuwen, Udren, Jenna I, Bennett, Siiri, Nelson, Sarah C, Gogarten, Stephanie M, Conomos, Matthew P, Heagerty, Patrick, Manolio, Teri, Pasquale, Louis R, Haiman, Christopher A, Caporaso, Neil, Weir, Bruce S

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In Situ Observation of Topotactic Linker Reorganization in the Aperiodic Metal–Organic Framework TRUMOF‑1 von Greenbaum, Guy, Doheny, Patrick W., Paraoan, Robert A. I., Kholina, Yevheniia, Michalik, Stefan, Cassidy, Simon J., Yeung, Hamish H.-M., Goodwin, Andrew L.

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Identification of candidate regions for familial idiopathic scoliosis von MILLER, Nancy H, JUSTICE, Cristina M, MAROSY, Beth, DOHENY, Kimberly F, PUGH, Elizabeth, JUN ZHANG, DIETZ, Harry C, WILSON, Alexander F

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