Congenital insensitivity to pain: Fracturing without apparent skeletal pathobiology caused by an autosomal dominant, second mutation in SCN11A encoding voltage-gated sodium channel... by Phatarakijnirund, Voraluck, Mumm, Steven, McAlister, William H, Novack, Deborah V, Wenkert, Deborah, Clements, Karen L, Whyte, Michael P

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Bisphosphonate‐Induced Osteopetrosis: Novel Bone Modeling Defects, Metaphyseal Osteopenia, and Osteosclerosis Fractures After Drug Exposure Ceases by Whyte, Michael P, McAlister, William H, Novack, Deborah V, Clements, Karen L, Schoenecker, Perry L, Wenkert, Deborah

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Coalescing expansile skeletal disease: Delineation of an extraordinary osteopathy involving the IFITM5 mutation of osteogenesis imperfecta type V by Whyte, Michael P., Aronson, James, McAlister, William H., Weinstein, Robert S., Wenkert, Deborah, Clements, Karen L., Gottesman, Gary S., Madson, Katherine L., Stolina, Marina, Bijanki, Vinieth N., Plotkin, Horacio, Huskey, Margaret, Duan, Shenghui, Mumm, Steven

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Prize-based contingency management for the treatment of substance abusers: a meta-analysis by Benishek, Lois A., Dugosh, Karen L., Kirby, Kim C., Matejkowski, Jason, Clements, Nicolle T., Seymour, Brittany L., Festinger, David S.

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Trial Watch: Oncolytic viro-immunotherapy of hematologic and solid tumors by Pol, Jonathan G., Lévesque, Sarah, Workenhe, Samuel T., Gujar, Shashi, Le Boeuf, Fabrice, Clements, Derek R., Fahrner, Jean-Eudes, Fend, Laetitia, Bell, John C., Mossman, Karen L., Fucikova, Jitka, Spisek, Radek, Zitvogel, Laurence, Kroemer, Guido, Galluzzi, Lorenzo

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Pregnancy Outcomes Among Women with Intellectual and Developmental Disabilities by Mitra, Monika, PhD, Parish, Susan L., PhD, MSW, Clements, Karen M., ScD, MPH, Cui, Xiaohui, ScD, Diop, Hafsatou, MD, MPH

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Postpartum Health Care Among Women With Intellectual and Developmental Disabilities by Clements, Karen M., Mitra, Monika, Zhang, Jianying, Parish, Susan L.

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Blinded, Multicenter Evaluation of Drug-induced Changes in Contractility Using Human-induced Pluripotent Stem Cell-derived Cardiomyocytes by Saleem, Umber, van Meer, Berend J, Katili, Puspita A, Mohd Yusof, Nurul A N, Mannhardt, Ingra, Garcia, Ana Krotenberg, Tertoolen, Leon, de Korte, Tessa, Vlaming, Maria L H, McGlynn, Karen, Nebel, Jessica, Bahinski, Anthony, Harris, Kate, Rossman, Eric, Xu, Xiaoping, Burton, Francis L, Smith, Godfrey L, Clements, Peter, Mummery, Christine L, Eschenhagen, Thomas, Hansen, Arne, Denning, Chris

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Building of a new Spectra for the identification of Phytobacter spp., an emerging Enterobacterales, using MALDI Biotyper by Dal Lin, A, Kulek, D O, Gonçalves, G A, Kraft, L, Neto, J F C, Vizentainer, G, Pillonetto, M

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Thioredoxin-interacting protein promotes high-glucose-induced macrovascular endothelial dysfunction by Li, Xiaoyu, Kover, Karen L., Heruth, Daniel P., Watkins, Dara J., Guo, Yanchun, Moore, Wayne V., He, Luke G., Zang, Mengwei, Clements, Mark A., Yan, Yun

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Global Levels of Specific Histone Modifications and an Epigenetic Gene Signature Predict Prostate Cancer Progression and Development by BIANCO-MIOTTO, Tina, CHIAM, Karen, HORVATH, Lisa G, KENCH, James G, STRICKER, Phillip D, MARSHALL, Villis R, SUTHERLAND, Robert L, HENSHALL, Susan M, GERALD, William L, SCHER, Howard I, RISBRIDGER, Gail P, CLEMENTS, Judith A, BUCHANAN, Grant, BUTLER, Lisa M, TILLEY, Wayne D, HORSFALL, David J, RICCIARDELLI, Carmela, JINDAL, Shalini, DAY, Tanya K, THOMAS, Mervyn, PICKERING, Marie A, O'LOUGHLIN, Melissa A, RYAN, Natalie K, RAYMOND, Wendy A

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Antenatal Hospitalization Among U.S. Women With Intellectual and Developmental Disabilities: A Retrospective Cohort Study by Mitra, Monika, Parish, Susan L, Clements, Karen M, Zhang, Jianying, Simas, Tiffany A Moore

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New Insight Into Metformin Action: Regulation of ChREBP and FOXO1 Activities in Endothelial Cells by Li, Xiaoyu, Kover, Karen L, Heruth, Daniel P, Watkins, Dara J, Moore, Wayne V, Jackson, Kathyrin, Zang, Mengwei, Clements, Mark A, Yan, Yun

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Clinical impact of COVID-19 on patients with cancer (CCC19): a cohort study by Choueiri, Toni K, Shyr, Yu, Grivas, Petros, Thompson, Michael A, Bilen, Mehmet A, Bouganim, Nathaniel, Doroshow, Deborah B, Egan, Pamela C, Elkrief, Arielle, Farmakiotis, Dimitrios, Glover, Michael J, Griffiths, Elizabeth A, Gulati, Anthony P, Gupta, Shilpa, Hsu, Emily, Lemmon, Christopher A, Lewis, Colleen, Masters, Tyler, Mesa, Ruben A, Morgans, Alicia K, Reynolds, Kerry, Rosen, Lane R, Schmidt, Andrew, Shaya, Justin A, Wulff-Burchfield, Elizabeth, Xie, Zhuoer, Yu, Peter P, Zubiri, Leyre, Warner, Jeremy L, Acoba, Jared D., Agarwal, Neeraj, Ahmad, Syed, Ajmera, Archana, Angevine, Anne H., Azad, Nilo, Barnholtz-Sloan, Jill, Barrow, Briana, Boland, Genevieve, Bonnen, Mark, Bouchard, Gabrielle, Busser, Fiona, Casulo, Carla, Curran, Catherine, Deeken, John, Demetri, George D., DiLullo, Sandy, Elias, Rawad, Feldman, Lawrence E., Friese, Christopher R., Fu, Paul, Gillaspie, Erin A., Giordano, Antonio, Glace, (Mary) Grace, Gurley, Michael, Halmos, Balazs, Johnson, Douglas B., Koshkin, Vadim S., Leighton, John C., Li, Xuanyi, LoRusso, Patricia, Low, Clarke A., Mansoor, Abdul-Hai, Handy Marshall, Catherine, Matar, Sara, McNair, Christopher, Mehnert, Janice M., Menon, Harry, Nagle, Sarah, Nakayama, John M., Nelson, Heather H., Nemecek, Eneida R., Nuzzo, Pier Vitale, Oberstein, Paul E., Owenby, Susie, Pasquinelli, Mary M., Revankar, Sanjay G., Rho, Young Soo, Rhodes, Terence D., Rice, Robert L., Riess, Jonathan, Routy, Bertrand, Rovito, Marc A., Saif, M. Wasif, Sanyal, Amit, Serrano, Oscar, Shah, Mansi, Shaw, Grace, Shergill, Ardaman, Stauffer, Karen, Stratton, Jamie, Stratton, Catherine, Subbiah, Vivek, Tannir, Nizar M., Van Allen, Eli, Verma, Amit K., Vikas, Praveen, Weiss, Matthias, Wise-Draper, Trisha, Wood, William A., Zacks, Rosemary

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Postpartum emergency department use among women with intellectual and developmental disabilities: a retrospective cohort study by Mitra, Monika, Akobirshoev, Ilhom, Parish, Susan L, Valentine, Anne, Clements, Karen M, Moore Simas, Tiffany A

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Canine Brachycephaly Is Associated with a Retrotransposon-Mediated Missplicing of SMOC2 by Marchant, Thomas W., Johnson, Edward J., McTeir, Lynn, Johnson, Craig I., Gow, Adam, Liuti, Tiziana, Kuehn, Dana, Svenson, Karen, Bermingham, Mairead L., Drögemüller, Michaela, Nussbaumer, Marc, Davey, Megan G., Argyle, David J., Powell, Roger M., Guilherme, Sérgio, Lang, Johann, Ter Haar, Gert, Leeb, Tosso, Schwarz, Tobias, Mellanby, Richard J., Clements, Dylan N., Schoenebeck, Jeffrey J.

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A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants by Chawner, Samuel J.R.A, Doherty, Joanne L, Anney, Richard J. L, Antshel, Kevin M, Bearden, Carrie E, Bernier, Raphael, Chung, Wendy K, Clements, Caitlin C, Curran, Sarah R, Cuturilo, Goran, Fiksinski, Ania M, Gallagher, Louise, Goin-Kochel, Robin P, Gur, Raquel E, Hanson, Ellen, Jacquemont, Sebastien, Kates, Wendy R, Kushan, Leila, Maillard, Anne M, McDonald-McGinn, Donna M, Mihaljevic, Marina, Miller, Judith S, Moss, Hayley, Pejovic-Milovancevic, Milica, Schultz, Robert T, Green-Snyder, LeeAnne, Vorstman, Jacob A, Wenger, Tara L, Hall, Jeremy, Owen, Michael J, van den Bree, Marianne B.M

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Whole-genome sequencing of a sporadic primary immunodeficiency cohort by 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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Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations by Lorenzini, Tiziana, Fliegauf, Manfred, Klammer, Nils, Proietti, Michele, Bulashevska, Alla, Schejter, Yael D., Atschekzei, Faranaz, Stepensky, Polina, Pedroza, Luis A., van der Flier, Michiel, Martínez-Gallo, Mónica, Svec, Peter, Fischer, Ute, Ip, Winnie, Geha, Raif, Chou, Janet, Alosaimi, Mohammed, Weintraub, Lauren, Dos Santos Vilela, Maria Marluce, Holzinger, Dirk, Seidl, Maximilian, Lougaris, Vassilios, Plebani, Alessandro, Abolhassani, Hassan, Thaventhiran, James E., Warnatz, Klaus, Grimbacher, Bodo, Ashford, Sofie, Bacchelli, Chiara, Batista, Joana, Bibi, Shahnaz, Boardman, Barbara, Booth, Claire, Breen, Gerome, Burns, Siobhan O., Burren, Oliver S., Carss, Keren, Chambers, John, Cooper, Nichola, Davies, E.G., Dempster, John, Dewhurst, Eleanor F., Drewe, Elizabeth, Duarte, Daniel, Edgar, J. David M., Egner, William, El-Shanawany, Tariq, Erwood, Marie, Fox, James, Frontini, Mattia, Furnell, Abigail, Gaspar, H. Bobby, Gleadall, Nicholas S., Grigoriadou, Sofia, Hackett, Scott, Hague, Rosie, Haimel, Matthias, Hayman, Grant, Hu, Fengyuan, Huissoon, Aarnoud P., Jolles, Stephen, Kasanicki, Mary A., Kelleher, Peter, Klein, Nigel, Kreuzhuber, Roman, Kuijpers, Taco W., Kumararatne, Dinakantha, Allen, Hana Lango, Linger, Rachel, Lorenzo, Lorena E., Maimaris, Jesmeen, Martin, Jennifer, McDermott, Elizabeth M., Meacham, Stuart, Morrisson, Valerie, Nasir, Iman, Nejentsev, Sergey, Papadia, Sofia, Ponsford, Mark J., Quinn, Ellen, Quinti, Isabella, Rayner-Matthews, Paula J., Samani, Nilesh, Sanchis-Juan, Alba, Savic, Sinisa, Simpson, Michael A., Smith, Kenneth G.C., Thaventhiran, James E., Tilly, Tobias, Titterton, Catherine, Tuna, Salih, Urniaz, Rafal, von Ziegenweidt, Julie, Watt, Christopher, Welch, Steven B., Whitehorn, Deborah, Wood, Yvette, Workman, Sarita, Worth, Austen, Young, Timothy

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Antepartum dalteparin versus no antepartum dalteparin for the prevention of pregnancy complications in pregnant women with thrombophilia (TIPPS): a multinational open-label randomi... by Rodger, Marc A, Prof, Hague, William M, Prof, Kingdom, John, Prof, Kahn, Susan R, Prof, Karovitch, Alan, MD, Sermer, Mathew, Prof, Clement, Anne Marie, RN, Coat, Suzette, PhD, Chan, Wee Shian, MD, Said, Joanne, MBBS, Rey, Evelyne, MD, Robinson, Sue, Prof, Khurana, Rshmi, MD, Demers, Christine, MD, Kovacs, Michael J, Prof, Solymoss, Susan, MD, Hinshaw, Kim, MBBS, Dwyer, James, MBBS, Smith, Graeme, Prof, McDonald, Sarah, MD, Newstead-Angel, Jill, MD, McLeod, Anne, MD, Khandelwal, Meena, Prof, Silver, Robert M, Prof, Le Gal, Gregoire, Prof, Greer, Ian A, Prof, Keely, Erin, Prof, Rosene-Montella, Karen, Prof, Walker, Mark, MD, Wells, Philip S, Prof

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