Pelvic function in anuran jumping: Interspecific differences in the kinematics and motor control of the iliosacral articulation during take-off and landing von Reilly, Steve M., Montuelle, Stephane J., Schmidt, Andre, Krause, Cornelia, Naylor, Emily, Jorgensen, Michael E., Essner Jr, Richard L.

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Interleukin-6 Is a Risk Factor for Atrial Fibrillation in Chronic Kidney Disease: Findings from the CRIC Study von Amdur, Richard L, Mukherjee, Monica, Go, Alan, Barrows, Ian R, Ramezani, Ali, Shoji, Jun, Reilly, Muredach P, Gnanaraj, Joseph, Deo, Raj, Roas, Sylvia, Keane, Martin, Master, Steve, Teal, Valerie, Soliman, Elsayed Z, Yang, Peter, Feldman, Harold, Kusek, John W, Tracy, Cynthia M, Raj, Dominic S

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Definition of subtypes of essential thrombocythaemia and relation to polycythaemia vera based on JAK2 V617F mutation status: a prospective study von Campbell, Peter J, Scott, Linda M, Buck, Georgina, Wheatley, Keith, East, Clare L, Marsden, Joanne T, Duffy, Audrey, Boyd, Elaine M, Bench, Anthony J, Scott, Mike A, Vassiliou, George S, Milligan, Donald W, Smith, Steve R, Erber, Wendy N, Bareford, David, Wilkins, Bridget S, Reilly, John T, Harrison, Claire N, Green, Anthony R

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Psychometric properties of the 16-item Quick Inventory of Depressive Symptomatology: A systematic review and meta-analysis von Reilly, Thomas J, MacGillivray, Steve A, Reid, Ian C, Cameron, Isobel M

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Selective blockade of TRPA1 channel attenuates pathological pain without altering noxious cold sensation or body temperature regulation von Chen, Jun, Joshi, Shailen K., DiDomenico, Stanley, Perner, Richard J., Mikusa, Joe P., Gauvin, Donna M., Segreti, Jason A., Han, Ping, Zhang, Xu-Feng, Niforatos, Wende, Bianchi, Bruce R., Baker, Scott J., Zhong, Chengmin, Simler, Gricelda H., McDonald, Heath A., Schmidt, Robert G., McGaraughty, Steve P., Chu, Katharine L., Faltynek, Connie R., Kort, Michael E., Reilly, Regina M., Kym, Philip R.

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TESS Hunt for Young and Maturing Exoplanets (THYME). VI. An 11 Myr Giant Planet Transiting a Very-low-mass Star in Lower Centaurus Crux von Mann, Andrew W., Wood, Mackenna L., Schmidt, Stephen P., Barber, Madyson G., Owen, James E., Tofflemire, Benjamin M., Newton, Elisabeth R., Mamajek, Eric E., Bush, Jonathan L., Mace, Gregory N., Kraus, Adam L., Thao, Pa Chia, Vanderburg, Andrew, Llama, Joe, Johns-Krull, Christopher M., Prato, L., Stahl, Asa G., Tang, Shih-Yun, Fields, Matthew J., Collins, Karen A., Collins, Kevin I., Gan, Tianjun, Jensen, Eric L. N., Kamler, Jacob, Schwarz, Richard P., Furlan, Elise, Gnilka, Crystal L., Howell, Steve B., Lester, Kathryn V., Owens, Dylan A., Suarez, Olga, Mekarnia, Djamel, Guillot, Tristan, Abe, Lyu, Triaud, Amaury H. M. J., Johnson, Marshall C., Milburn, Reilly P., Rizzuto, Aaron C., Quinn, Samuel N., Kerr, Ronan, Ricker, George R., Vanderspek, Roland, Latham, David W., Seager, Sara, Winn, Joshua N., Jenkins, Jon M., Guerrero, Natalia M., Shporer, Avi, Schlieder, Joshua E., McLean, Brian, Wohler, Bill

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The International Mouse Phenotyping Consortium (IMPC): a functional catalogue of the mammalian genome that informs conservation von Muñoz-Fuentes, Violeta, Cacheiro, Pilar, Meehan, Terrence F., Aguilar-Pimentel, Juan Antonio, Brown, Steve D. M., Flenniken, Ann M., Flicek, Paul, Galli, Antonella, Mashhadi, Hamed Haseli, Hrabě de Angelis, Martin, Kim, Jong Kyoung, Lloyd, K. C. Kent, McKerlie, Colin, Morgan, Hugh, Murray, Stephen A., Nutter, Lauryl M. J., Reilly, Patrick T., Seavitt, John R., Seong, Je Kyung, Simon, Michelle, Wardle-Jones, Hannah, Mallon, Ann-Marie, Smedley, Damian, Parkinson, Helen E.

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Shared Genetic Susceptibility to Ischemic Stroke and Coronary Artery Disease: A Genome-Wide Analysis of Common Variants von DICHGANS, Martin, MALIK, Rainer, O'DONNELL, Christopher J, FORNAGE, Myriam, THORSTEINSDOTTIR, Unnur, PSATY, Bruce M, HENGSTENBERG, Christian, SESHADRI, Sudha, ERDMANN, Jeanette, BIS, Joshua C, PETERS, Annette, BONCORAGLIO, Giorgio B, KÖNIG, Inke R, MÄRZ, Winfried, MESCHIA, James F, KATHIRESAN, Sekar, IKRAM, M. Arfan, McPHERSON, Ruth, STEFANSSON, Kari, SUDLOW, Cathie, REILLY, Muredach P, THOMPSON, John R, SHARMA, Pankaj, ROSAND, Jonathan, HOPEWELL, Jemma C, CHAMBERS, John C, WATKINS, Hugh, ROTHWELL, Peter M, ROBERTS, Robert, MARKUS, Hugh S, SAMANI, Nilesh J, FARRALL, Martin, SCHUNKERT, Heribert, CLARKE, Robert, GRETARSDOTTIR, Solveig, THORLEIFSSON, Gudmar, MITCHELL, Braxton D, ASSIMES, Themistocles L, LEVI, Christopher

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Axonal excitability as an early biomarker of nerve involvement in hereditary transthyretin amyloidosis von Carroll, Antonia S., Park, Susanna B., Lin, Cindy S.Y., Taylor, Mark S., Kwok, Fiona, Simon, Neil G., Reilly, Mary M., Kiernan, Matthew C., Vucic, Steve

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TESS Hunt for Young and Maturing Exoplanets (THYME). IX. A 27 Myr Extended Population of Lower Centaurus Crux with a Transiting Two-planet System von Wood, Mackenna L., Mann, Andrew W., Barber, Madyson G., Bush, Jonathan L., Kraus, Adam L., Tofflemire, Benjamin M., Vanderburg, Andrew, Newton, Elisabeth R., Feiden, Gregory A., Zhou, George, Bouma, Luke G., Quinn, Samuel N., Armstrong, David J., Osborn, Ares, Adibekyan, Vardan, Mena, Elisa Delgado, Sousa, Sergio G., Gagné, Jonathan, Fields, Matthew J., Milburn, Reilly P., Thao, Pa Chia, Schmidt, Stephen P., Gnilka, Crystal L., Howell, Steve B., Law, Nicholas M., Ziegler, Carl, Briceño, César, Ricker, George R., Vanderspek, Roland, Latham, David W., Seager, Sara, Winn, Joshua N., Jenkins, Jon M., Schlieder, Joshua E., Osborn, Hugh P., Twicken, Joseph D., Ciardi, David R., Huang, Chelsea X.

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Improving clinical trial outcomes in amyotrophic lateral sclerosis von Kiernan, Matthew C., Vucic, Steve, Talbot, Kevin, McDermott, Christopher J., Hardiman, Orla, Shefner, Jeremy M., Al-Chalabi, Ammar, Huynh, William, Cudkowicz, Merit, Talman, Paul, Van den Berg, Leonard H., Dharmadasa, Thanuja, Wicks, Paul, Reilly, Claire, Turner, Martin R.

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Whole-genome sequencing of a sporadic primary immunodeficiency cohort von Thaventhiran, James E. D., Lango Allen, Hana, Burren, Oliver S., Rae, William, Greene, Daniel, Staples, Emily, Zhang, Zinan, Farmery, James H. R., Simeoni, Ilenia, Rivers, Elizabeth, Maimaris, Jesmeen, Penkett, Christopher J., Stephens, Jonathan, Deevi, Sri V. V., Sanchis-Juan, Alba, Gleadall, Nicholas S., Thomas, Moira J., Sargur, Ravishankar B., Gordins, Pavels, Baxendale, Helen E., Brown, Matthew, Tuijnenburg, Paul, Worth, Austen, Hanson, Steven, Linger, Rachel J., Buckland, Matthew S., Rayner-Matthews, Paula J., Gilmour, Kimberly C., Samarghitean, Crina, Seneviratne, Suranjith L., Sansom, David M., Lynch, Andy G., Megy, Karyn, Ellinghaus, Eva, Ellinghaus, David, Jorgensen, Silje F., Karlsen, Tom H., Stirrups, Kathleen E., Cutler, Antony J., Kumararatne, Dinakantha S., Chandra, Anita, Edgar, J. David M., Herwadkar, Archana, Cooper, Nichola, Grigoriadou, Sofia, Huissoon, Aarnoud P., Goddard, Sarah, Jolles, Stephen, Schuetz, Catharina, Boschann, Felix, Lyons, Paul A., Hurles, Matthew E., Savic, Sinisa, Burns, Siobhan O., Kuijpers, Taco W., Turro, Ernest, Ouwehand, Willem H., Thrasher, Adrian J., Smith, Kenneth G. C.

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Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes von Cortese, Andrea, Zhu, Yi, Rebelo, Adriana P., Negri, Sara, Courel, Steve, Abreu, Lisa, Bacon, Chelsea J., Bai, Yunhong, Bis-Brewer, Dana M., Bugiardini, Enrico, Buglo, Elena, Danzi, Matt C., Feely, Shawna M. E., Athanasiou-Fragkouli, Alkyoni, Haridy, Nourelhoda A., Isasi, Rosario, Khan, Alaa, Laurà, Matilde, Magri, Stefania, Pipis, Menelaos, Pisciotta, Chiara, Powell, Eric, Rossor, Alexander M., Saveri, Paola, Sowden, Janet E., Tozza, Stefano, Vandrovcova, Jana, Dallman, Julia, Grignani, Elena, Marchioni, Enrico, Scherer, Steven S., Tang, Beisha, Lin, Zhiqiang, Al-Ajmi, Abdullah, Schüle, Rebecca, Synofzik, Matthis, Maisonobe, Thierry, Stojkovic, Tanya, Auer-Grumbach, Michaela, Abdelhamed, Mohamed A., Hamed, Sherifa A., Zhang, Ruxu, Manganelli, Fiore, Santoro, Lucio, Taroni, Franco, Pareyson, Davide, Houlden, Henry, Herrmann, David N., Reilly, Mary M., Shy, Michael E., Zhai, R. Grace, Zuchner, Stephan

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Normal and pathogenic variation of RFC1 repeat expansions: implications for clinical diagnosis von Dominik, Natalia, Magri, Stefania, Currò, Riccardo, Abati, Elena, Facchini, Stefano, Corbetta, Marinella, Macpherson, Hannah, Di Bella, Daniela, Sarto, Elisa, Stevanovski, Igor, Chintalaphani, Sanjog R, Akcimen, Fulya, Manini, Arianna, Vegezzi, Elisa, Quartesan, Ilaria, Montgomery, Kylie-Ann, Pirota, Valentina, Crespan, Emmanuele, Perini, Cecilia, Grupelli, Glenda Paola, Tomaselli, Pedro J, Marques, Wilson, Shaw, Joseph, Polke, James, Salsano, Ettore, Fenu, Silvia, Pareyson, Davide, Pisciotta, Chiara, Tofaris, George K, Nemeth, Andrea H, Ealing, John, Radunovic, Aleksandar, Kearney, Seamus, Kumar, Kishore R, Vucic, Steve, Kennerson, Marina, Reilly, Mary M, Houlden, Henry, Deveson, Ira, Tucci, Arianna, Taroni, Franco, Cortese, Andrea

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Differences in nerve excitability properties across upper limb sensory and motor axons von Carroll, Antonia S., Howells, James, Lin, Cindy S.Y., Park, Susanna B., Simon, Neil, Reilly, Mary M., Vucic, Steve, Kiernan, Matthew C.

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Effects of diazepam on hippocampal blood flow in people at clinical high risk for psychosis von Livingston, Nicholas R, Kiemes, Amanda, Devenyi, Gabriel A, Knight, Samuel, Lukow, Paulina B, Jelen, Luke A, Reilly, Thomas, Dima, Aikaterini, Nettis, Maria Antonietta, Casetta, Cecilia, Agyekum, Tyler, Zelaya, Fernando, Spencer, Thomas, De Micheli, Andrea, Fusar-Poli, Paolo, Grace, Anthony A, Williams, Steve C R, McGuire, Philip, Egerton, Alice, Chakravarty, M Mallar, Modinos, Gemma

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A CADM3 variant causes Charcot-Marie-Tooth disease with marked upper limb involvement von Rebelo, Adriana P, Cortese, Andrea, Abraham, Amit, Eshed-Eisenbach, Yael, Shner, Gal, Vainshtein, Anna, Buglo, Elena, Camarena, Vladimir, Gaidosh, Gabriel, Shiekhattar, Ramin, Abreu, Lisa, Courel, Steve, Burns, Dennis K, Bai, Yunhong, Bacon, Chelsea, Feely, Shawna M E, Castro, Diana, Peles, Elior, Reilly, Mary M, Shy, Michael E, Zuchner, Stephan

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Soft windowing application to improve analysis of high-throughput phenotyping data von Haselimashhadi, Hamed, Mason, Jeremy C, Munoz-Fuentes, Violeta, López-Gómez, Federico, Babalola, Kolawole, Acar, Elif F, Kumar, Vivek, White, Jacqui, Flenniken, Ann M, King, Ruairidh, Straiton, Ewan, Seavitt, John Richard, Gaspero, Angelina, Garza, Arturo, Christianson, Audrey E, Hsu, Chih-Wei, Reynolds, Corey L, Lanza, Denise G, Lorenzo, Isabel, Green, Jennie R, Gallegos, Juan J, Bohat, Ritu, Samaco, Rodney C, Veeraragavan, Surabi, Kim, Jong Kyoung, Miller, Gregor, Fuchs, Helmult, Garrett, Lillian, Becker, Lore, Kang, Yeon Kyung, Clary, David, Cho, Soo Young, Tamura, Masaru, Tanaka, Nobuhiko, Soo, Kyung Dong, Bezginov, Alexandr, About, Ghina Bou, Champy, Marie-France, Vasseur, Laurent, Leblanc, Sophie, Meziane, Hamid, Selloum, Mohammed, Reilly, Patrick T, Spielmann, Nadine, Maier, Holger, Gailus-Durner, Valerie, Sorg, Tania, Hiroshi, Masuya, Yuichi, Obata, Heaney, Jason D, Dickinson, Mary E, Wolfgang, Wurst, Tocchini-Valentini, Glauco P, Lloyd, Kevin C Kent, McKerlie, Colin, Seong, Je Kyung, Yann, Herault, de Angelis, Martin Hrabé, Brown, Steve D M, Smedley, Damian, Flicek, Paul, Mallon, Ann-Marie, Parkinson, Helen, Meehan, Terrence F

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Estimating GFR Among Participants in the Chronic Renal Insufficiency Cohort (CRIC) Study von Anderson, Amanda Hyre, PhD, Yang, Wei, PhD, Hsu, Chi-yuan, MD, MSc, Joffe, Marshall M., MD, PhD, MPH, Leonard, Mary B., MD, MSCE, Xie, Dawei, PhD, Chen, Jing, MD, MSc, Greene, Tom, PhD, Jaar, Bernard G., MD, MPH, Kao, Patricia, MD, Kusek, John W., PhD, Landis, J. Richard, PhD, Lash, James P., MD, Townsend, Raymond R., MD, Weir, Matthew R., MD, Feldman, Harold I., MD, MSCE

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Assessing non-Mendelian inheritance in inherited axonopathies von Bis-Brewer, Dana M., Gan-Or, Ziv, Sleiman, Patrick, Hakonarson, Hakon, Fazal, Sarah, Courel, Steve, Cintra, Vivian, Tao, Feifei, Estiar, Mehrdad A., Tarnopolsky, Mark, Boycott, Kym M., Yoon, Grace, Suchowersky, Oksana, Dupré, Nicolas, Cheng, Andrew, Lloyd, Thomas E., Rouleau, Guy, Schüle, Rebecca, Züchner, Stephan

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