Fibro-Osseous Lesions of the Craniofacial Bones: β-Catenin Immunohistochemical Analysis and CTNNB1 and APC Mutation Analysis

by E Horvai, Andrew, C Jordan, Richard
Published in Head & neck pathology (Totowa, N.J.)

Genomic Profiling of the Craniofacial Ossifying Fibroma by Next-Generation Sequencing

by Bahceci, Dorukhan H., Grenert, James P., Jordan, Richard C. K., Horvai, Andrew E.
Published in Head & neck pathology (Totowa, N.J.)

Targeting JAK1/2 and mTOR in murine xenograft models of Ph-like acute lymphoblastic leukemia

by Maude, Shannon L., Tasian, Sarah K., Vincent, Tiffaney, Hall, Junior W., Sheen, Cecilia, Roberts, Kathryn G., Seif, Alix E., Barrett, David M., Chen, I-Ming, Collins, J. Racquel, Mullighan, Charles G., Hunger, Stephen P., Harvey, Richard C., Willman, Cheryl L., Fridman, Jordan S., Loh, Mignon L., Grupp, Stephan A., Teachey, David T.
Published in Blood

Genetic and mechanistic diversity in pediatric hemophagocytic lymphohistiocytosis

by Chinn, Ivan K., Eckstein, Olive S., Peckham-Gregory, Erin C., Goldberg, Baruch R., Forbes, Lisa R., Nicholas, Sarah K., Mace, Emily M., Vogel, Tiphanie P., Abhyankar, Harshal A., Diaz, Maria I., Heslop, Helen E., Krance, Robert A., Martinez, Caridad A., Nguyen, Trung C., Bashir, Dalia A., Goldman, Jordana R., Stray-Pedersen, Asbjørg, Pedroza, Luis A., Poli, M. Cecilia, Aldave-Becerra, Juan C., McGhee, Sean A., Al-Herz, Waleed, Chamdin, Aghiad, Coban-Akdemir, Zeynep H., Jhangiani, Shalini N., Muzny, Donna M., Cao, Tram N., Hong, Diana N., Gibbs, Richard A., Lupski, James R., Orange, Jordan S., McClain, Kenneth L., Allen, Carl E.
Published in Blood

The Minderoo-Monaco Commission on Plastics and Human Health

by Landrigan, Philip J, Raps, Hervé, Cropper, Maureen, Bald, Caroline, Brunner, Manuel, Canonizado, Elvia Maya, Charles, Dominic, Chiles, Thomas C, Donohue, Mary J, Enck, Judith, Fenichel, Patrick, Fleming, Lora E, Ferrier-Pages, Christine, Fordham, Richard, Gozt, Aleksandra, Griffin, Carly, Hahn, Mark E, Haryanto, Budi, Hixson, Richard, Ianelli, Hannah, James, Bryan D, Kumar, Pushpam, Laborde, Amalia, Law, Kara Lavender, Martin, Keith, Mu, Jenna, Mulders, Yannick, Mustapha, Adetoun, Niu, Jia, Pahl, Sabine, Park, Yongjoon, Pedrotti, Maria-Luiza, Pitt, Jordan Avery, Ruchirawat, Mathuros, Seewoo, Bhedita Jaya, Spring, Margaret, Stegeman, John J, Suk, William, Symeonides, Christos, Takada, Hideshige, Thompson, Richard C, Vicini, Andrea, Wang, Zhanyun, Whitman, Ella, Wirth, David, Wolff, Megan, Yousuf, Aroub K, Dunlop, Sarah
Published in Annals of global health

Hepatic Cytochrome P450 Activity, Abundance, and Expression Throughout Human Development

by Sadler, Natalie C, Nandhikonda, Premchendar, Webb-Robertson, Bobbie-Jo, Ansong, Charles, Anderson, Lindsey N, Smith, Jordan N, Corley, Richard A, Wright, Aaron T
Published in Drug metabolism and disposition

A pharmacokinetic simulation study to assess the performance of a sparse blood sampling approach to quantify early drug exposure

by Sathe, Abhishek G., Brundage, Richard C., Ivaturi, Vijay, Cloyd, James C., Chamberlain, James M., Elm, Jordan J., Silbergleit, Robert, Kapur, Jaideep, Coles, Lisa D.
Published in Clinical and translational science

Management of Sickle Cell Disease: Summary of the 2014 Evidence-Based Report by Expert Panel Members

by Yawn, Barbara P, Buchanan, George R, Afenyi-Annan, Araba N, Ballas, Samir K, Hassell, Kathryn L, James, Andra H, Jordan, Lanetta, Lanzkron, Sophie M, Lottenberg, Richard, Savage, William J, Tanabe, Paula J, Ware, Russell E, Murad, M. Hassan, Goldsmith, Jonathan C, Ortiz, Eduardo, Fulwood, Robinson, Horton, Ann, John-Sowah, Joylene
Published in JAMA : the journal of the American Medical Association

Early Exposure of Fosphenytoin, Levetiracetam, and Valproic Acid After High‐Dose Intravenous Administration in Young Children With Benzodiazepine‐Refractory Status Epilepticus

by Sathe, Abhishek G., Mishra, Usha, Ivaturi, Vijay, Brundage, Richard C., Cloyd, James C., Elm, Jordan J., Chamberlain, James M., Silbergleit, Robert, Kapur, Jaideep, Lowenstein, Daniel H., Shinnar, Shlomo, Cock, Hannah R., Fountain, Nathan B., Babcock, Lynn, Coles, Lisa D.
Published in Journal of clinical pharmacology

Clinical characteristics of children and young people admitted to hospital with covid-19 in United Kingdom: prospective multicentre observational cohort study

by Swann, Olivia V, Holden, Karl A, Turtle, Lance, Pollock, Louisa, Fairfield, Cameron J, Drake, Thomas M, Seth, Sohan, Egan, Conor, Hardwick, Hayley E, Halpin, Sophie, Girvan, Michelle, Donohue, Chloe, Pritchard, Mark, Patel, Latifa B, Ladhani, Shamez, Sigfrid, Louise, Sinha, Ian P, Olliaro, Piero L, Nguyen-Van-Tam, Jonathan S, Horby, Peter W, Merson, Laura, Carson, Gail, Dunning, Jake, Openshaw, Peter J M, Baillie, J Kenneth, Harrison, Ewen M, Docherty, Annemarie B, Semple, Malcolm G
Published in BMJ

Genetic errors of immunity distinguish pediatric nonmalignant lymphoproliferative disorders

by Forbes, Lisa R., Eckstein, Olive S., Gulati, Nitya, Peckham-Gregory, Erin C., Ozuah, Nmazuo W., Lubega, Joseph, El-Mallawany, Nader K., Agrusa, Jennifer E., Poli, M. Cecilia, Vogel, Tiphanie P., Chaimowitz, Natalia S., Rider, Nicholas L., Mace, Emily M., Orange, Jordan S., Caldwell, Jason W., Aldave-Becerra, Juan C., Jolles, Stephen, Saettini, Francesco, Chong, Hey J., Stray-Pedersen, Asbjorg, Heslop, Helen E., Kamdar, Kala Y., Rouce, R. Helen, Muzny, Donna M., Jhangiani, Shalini N., Gibbs, Richard A., Coban-Akdemir, Zeynep H., Lupski, James R., McClain, Kenneth L., Allen, Carl E., Chinn, Ivan K.
Published in Journal of allergy and clinical immunology

Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes

by Phillips, Jennifer B., Lanza, Denise G., Jain, Mahim, Raman, Vandana, Chitayat, David, Chinn, Ivan K., Bertuch, Alison A., Bamshad, Michael, Savarirayan, Ravi, Doddapaneni, Harsha, Muzny, Donna, Gibbs, Richard A., Rosenfeld, Jill A., Postlethwait, John, Beaudet, Arthur L., Ranza, Emmanuelle, Cormier-Daire, Valérie, Orange, Jordan S., Allard, Patrick, Barseghyan, Hayk, Batzli, Gabriel F., Beggs, Alan H., Bellen, Hugo J., Bernstein, Jonathan A., Bick, David P., Briere, Lauren C., Brokamp, Elly, Brush, Matthew, Coakley, Terra R., Cope, Heidi, Davidson, Jean M., Dayal, Jyoti G., Dhar, Shweta U., Dipple, Katrina M., Dorrani, Naghmeh, Duncan, Laura, Emrick, Lisa T., Eng, Christine M., Enns, Gregory M., Fisher, Paul G., Friedman, Noah D., Gahl, William A., Glanton, Emily, Goldman, Alica M., Gourdine, Jean-Philippe F., Groden, Catherine A., Haendel, Melissa, Hamid, Rizwan, High, Frances, Huang, Yong, Karaviti, Lefkothea, Kohler, Jennefer N., Krasnewich, Donna M., Korrick, Susan, Krier, Joel B., Kyle, Jennifer E., Lau, C. Christopher, Lee, Hane, Loo, Sandra K., Loscalzo, Joseph, Martin, Martin G., Martínez-Agosto, Julian A., Marwaha, Shruti, McCormack, Colleen E., McCray, Alexa T., Metz, Thomas O., Murdock, David R., Newberry, J. Scott, Nicholas, Sarah K., Palmer, Christina G.S., Papp, Jeanette C., Phillips, John A., Posey, Jennifer E., Pusey, Barbara N., Sampson, Jacinda B., Shakachite, Lisa, Signer, Rebecca, Silverman, Edwin K., Spillmann, Rebecca C., Stoler, Joan M., Stong, Nicholas, Sweetser, David A., Tan, Queenie K.-G., Tran, Alyssa A., Vogel, Tiphanie P., Wahl, Colleen E., Wangler, Michael F., Waters, Katrina M., Westerfield, Monte, Wise, Anastasia L., Yang, John, Yang, Yaping, Yoon, Amanda J., Zastrow, Diane B., Zhao, Chunli, Offiah, Amaka C., Carey, John C., Bacino, Carlos A., Campeau, Philippe M., Lee, Brendan
Published in American journal of human genetics

A comprehensive iterative approach is highly effective in diagnosing individuals who are exome negative

by Schoch, Kelly, Spillmann, Rebecca, Tan, Queenie K.-G., McConkie-Rosell, Allyn, Jiang, Yong-Hui, Goldstein, David B., Adams, David R., Allard, Patrick, Ashley, Euan A., Bacino, Carlos A., Beggs, Alan H., Birch, Camille L., Bonner, Devon, Boone, Braden E., Brown, Donna M., Chen, Shan, Coakley, Terra R., Cogan, Joy D., Cooper, Cynthia M., Cope, Heidi, Craigen, William J., Davidson, Jean M., Dayal, Jyoti G., Dell’Angelica, Esteban C., Dipple, Katrina M., Donnell-Fink, Laurel A., Dorrani, Naghmeh, Draper, David D., Dries, Annika M., Eckstein, David J., Emrick, Lisa T., Enns, Gregory M., Esteves, Cecilia, Estwick, Tyra, Fernandez, Liliana, Ferreira, Carlos, Fisher, Paul G., Fogel, Brent L., Friedman, Noah D., Gahl, William A., Goldstein, David B., Gourdine, Jean-Philippe F., Haendel, Melissa, Handley, Lori H., Krasnewich, Donna M., Krier, Joel B., Lazar, Jozef, Levy, Shawn E., Lincoln, Sharyn A., Loo, Sandra K., Loscalzo, Joseph, Maas, Richard L., MacRae, Calum A., Majcherska, Marta M., Mamounas, Laura A., Manolio, Teri A., Markello, Thomas C., Marom, Ronit, Martin, Martin G., McConkie-Rosell, Allyn, McCormack, Colleen E., Might, Matthew, Morimoto, Marie, Mulvihill, John J., Murphy, Jennifer L., Muzny, Donna M., Nehrebecky, Michele E., Nelson, Stan F., Newberry, J. Scott, Newman, John H., Nicholas, Sarah K., Pallais, J. Carl, Palmer, Christina GS, Parker, Neil H., Phillips, John A., Postlethwait, John H., Reuter, Chloe M., Sampson, Jacinda B., Scott, Daryl A., Sharma, Prashant, Shashi, Vandana, Silverman, Edwin K., Tifft, Cynthia J., Toro, Camilo, Tran, Alyssa A., Urv, Tiina K., Vogel, Tiphanie P., Wahl, Colleen E., Walsh, Chris A., Wan, Jijun, Wangler, Michael F., Ward, Patricia A., Wheeler, Matthew T., Wolfe, Lynne A., Worthey, Elizabeth A., Yamamoto, Shinya, Yang, Yaping, Yu, Guoyun, Zhao, Chunli, Zheng, Allison
Published in Genetics in medicine

A Syndromic Neurodevelopmental Disorder Caused by De Novo Variants in EBF3

by Davids, Mariska, Pappas, John G., Rosenfeld, Jill A., McCarty, Alexandra J., Tifft, Cynthia, Stong, Nicholas, Johnson, Travis K., Warr, Coral G., Adams, Christopher J., Alejandro, Mercedes E., Ashley, Euan A., Barseghyan, Hayk, Beggs, Alan H., Bernstein, Jonathan A., Briere, Lauren C., Brush, Matthew, Cogan, Joy D., Craigen, William J., Davids, Mariska, Dayal, Jyoti G., Dhar, Shweta U., Dipple, Katrina M., Donnell-Fink, Laurel A., Dorrani, Naghmeh, Eckstein, David J., Emrick, Lisa T., Eng, Christine M., Esteves, Cecilia, Fisher, Paul G., Frisby, Trevor S., Frost, Kate, Gahl, William A., Gartner, Valerie, Golas, Gretchen A., Gould, Sarah E., Graham, Brett H., Groden, Catherine A., Gropman, Andrea L., Haendel, Melissa, Hanchard, Neil A., Herzog, Matthew R., Jacob, Howard J., Jain, Mahim, Jiang, Yong-hui, Jones, Angela L., Koehler, Alanna E., Kohane, Isaac S., Krasnewich, Donna M., Krieg, Elizabeth L., Lau, C. Christopher, Lazar, Jozef, Lee, Brendan H., Levy, Denise J., Liebendorder, Adam P., Lincoln, Sharyn A., Loomis, Carson R., Loscalzo, Joseph, Macnamara, Ellen F., MacRae, Calum A., Malicdan, May Christine V., Mamounas, Laura A., Markello, Thomas C., Mazur, Paul, McCarty, Alexandra J., McCray, Alexa T., Metz, Thomas O., Moretti, Paolo M., Murphy, Jennifer L., Muzny, Donna M., Nehrebecky, Michele E., Pallais, J. Carl, Palmer, Christina G.S., Pena, Loren D.M., Phillips, John A., Posey, Jennifer E., Potocki, Lorraine, Pusey, Barbara N., Schoch, Kelly, Scott, Daryl A., Sharma, Prashant, Soldatos, Ariane G., Splinter, Kimberly, Strong, Kimberly A., Sullivan, Jennifer A., Sweetser, David A., Thomas, Sara P., Tift, Cynthia J., Tolman, Nathanial J., Toro, Camilo, Vilain, Eric, Walley, Nicole M., Webb-Robertson, Bobbie-Jo M., Weech, Alec A., Westerfield, Monte, Wheeler, Matt T., Yamamoto, Shinya, Yang, Yaping, Zornio, Patricia A., Yamamoto, Shinya, Malicdan, May Christine V.
Published in American journal of human genetics

Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay

by Sullivan, Jennifer A., Shashi, Vandana, Jiang, Yong-hui, Stong, Nicholas, Fiala, Elise, Willing, Marcia, Pfundt, Rolph, Kleefstra, Tjitske, Orellana, Carmen, Monfort, Sandra, Roscioli, Tony, Jones, Wendy D., Sebastian, Jessica, Sonal, Desai, Sakkubai, Naidu, Faivre, Laurence, Krantz, Ian D., Adams, David R., Alejandro, Mercedes E., Azamian, Mahshid S., Barseghyan, Hayk, Batzli, Gabriel F., Beggs, Alan H., Bican, Anna, Birch, Camille L., Bonner, Devon, Boone, Braden E., Briere, Lauren C., Brown, Donna M., Brush, Matthew, Chen, Shan, Coakley, Terra R., Cooper, Cynthia M., Cope, Heidi, Craigen, William J., Dayal, Jyoti G., Dell’Angelica, Esteban C., Dillon, Ani, Dipple, Katrina M., Donnell-Fink, Laurel A., Dorrani, Naghmeh, Dorset, Daniel C., Eskin, Ascia, Friedman, Noah D., Glanton, Emily, Godfrey, Rena A., Gould, Sarah E., Gropman, Andrea L., Hom, Jason, Jacob, Howard J., Jain, Mahim, Jiang, Yong-hui, Kohane, Isaac S., Krieg, Elizabeth L., Lau, C. Christopher, Lazar, Jozef, Lee, Brendan H., Lee, Hane, Lewis, Richard A., Loo, Sandra K., Majcherska, Marta M., Malicdan, May Christine V., Mamounas, Laura A., Markello, Thomas C., Martínez-Agosto, Julian A., Marwaha, Shruti, May, Thomas, McCray, Alexa T., Might, Matthew, Mulvihill, John J., Murphy, Jennifer L., Nelson, Stan F., Newman, John H., Novacic, Donna, Orange, Jordan S., Pallais, J. Carl, Pena, Loren D.M., Phillips, John A., Postlethwait, John H., Reuter, Chloe M., Rosenfeld, Jill A., Sharma, Prashant, Shashi, Vandana, Signer, Rebecca, Sinsheimer, Janet S., Spillmann, Rebecca C., Splinter, Kimberly, Stoler, Joan M., Stong, Nicholas, Sweetser, David A., Tran, Alyssa A., Valivullah, Zaheer M., Wahl, Colleen E., Waters, Katrina M., Westerfield, Monte, Wise, Anastasia L., Worthey, Elizabeth A., Yang, Yaping, Zastrow, Diane B., Campeau, Philippe M.
Published in American journal of human genetics

Inter-Rater Reliability of the CASCADE Criteria: Challenges in Classifying Arteriopathies

by Bernard, Timothy J, Beslow, Lauren A, Manco-Johnson, Marilyn J, Armstrong-Wells, Jennifer, Boada, Richard, Weitzenkamp, David, Hollatz, Amanda, Poisson, Sharon, Amlie-Lefond, Catherine, Lo, Warren, deVeber, Gabrielle, Goldenberg, Neil A, Dowling, Michael M, Roach, E Steve, Fullerton, Heather J, Benseler, Susanne M, Jordan, Lori C, Kirton, Adam, Ichord, Rebecca N
Published in Stroke (1970)

Precore and Basal Core Promoter Hepatitis B Virus (HBV) Variants Are Present From a Young Age and Differ Across HBV Genotypes

by Ganova‐Raeva, Lilia, Wang, Junyao, Mogul, Douglas, Lisker‐Melman, Mauricio, Chang, Kyong‐Mi, Janssen, Harry L.A., Wahed, Abdus S., Lok, Anna S., Niu, Jianghe, Nasser, Imad, Rusibamayila, Nifasha, Stahler, Alisha C, Stadheim, Linda, Lake, John, Riggs, Shannon M, Rushing, Kathryn, Cerkoski, Jacki, Shaw, Debra DeMarco, Noureldin, Seham, Kaznowski, Diana, Vladutu, Doinita, Cerocchi, Orlando, Bass, Sheila, Rodgers‐Augustyniak, Laurie A, Montanye, Shirley, Peters, Marion, Davis, Rayshawnda, Kuras, Romuald, Ayala, Claudia, Lau, Ivy, Podolskaya, Veronika, von Bakonyi, Anna, DeVole, Nata, Feier, Natasha, Feier, Joel, Oberhelman, Kelly, Kaza, Sravanthi, Huddleston, Leslie, Wong, Richmond, Marsh, Tiffany, Cardona, Danielle, Hofmann, Charlotte, Wolfstone, Alycia, Mooney, Jody, Cooper, Kara L, Imteyaz, Hejab, Oshima, Kiyoko, Kafka, Kim, Islam, Naureen, Fryzek, Nancy, Morris, Nevitt, Hoofnagle, Jay H, Doo, Edward, Torrance, Rebecca J, Valiga, Mary E, Keith, James, Betts, Michael, Montaner, Luis J, Averbach, Frani, Hardison, Regina, Lalama, Christina, Lawlor, Sharon, Lin, Hsing‐Hua S, Lombardero, Manuel, Pelesko, Andrew, Stoliker, Donna, Zhao, Qian, Roberts, Lewis R, Hassan, Mohamed A, Schwarzenberg, Sarah Jane, Di Bisceglie, Adrian M, Wong, David K, Feld, Jordan, Patel, Keyur, Ling, Simon C, Lee, William M, Murakami, Carol S, Perrillo, Robert, Do, Son, Han, Steven‐Huy B, Tran, Tram T, Terrault, Norah A, Khalili, Mandana, Rosenthal, Philip, Fontana, Robert J, Younoszai, Barak, Fried, Michael W, Muir, Andrew, Darling, Jama M, Carithers, Robert C, Shuhart, Margaret, Kowdley, Kris V, Murray, Karen F, Sterling, Richard K, Ghany, Marc G, Jake Liang, T, Hoofnagle, Jay H, Doo, Edward, King, Wendy C, Kleiner, David
Published in Hepatology (Baltimore, Md.)

Medulloblastoma Down Under 2013: a report from the third annual meeting of the International Medulloblastoma Working Group

by Gottardo, Nicholas G., Hansford, Jordan R., McGlade, Jacqueline P., Alvaro, Frank, Ashley, David M., Bailey, Simon, Baker, David L., Bourdeaut, Franck, Cho, Yoon-Jae, Clay, Moira, Clifford, Steven C., Cohn, Richard J., Cole, Catherine H., Dallas, Peter B., Downie, Peter, Doz, François, Ellison, David W., Endersby, Raelene, Fisher, Paul G., Hassall, Timothy, Heath, John A., Hii, Hilary L., Jones, David T. W., Junckerstorff, Reimar, Kellie, Stewart, Kool, Marcel, Kotecha, Rishi S., Lichter, Peter, Laughton, Stephen J., Lee, Sharon, McCowage, Geoff, Northcott, Paul A., Olson, James M., Packer, Roger J., Pfister, Stefan M., Pietsch, Torsten, Pizer, Barry, Pomeroy, Scott L., Remke, Marc, Robinson, Giles W., Rutkowski, Stefan, Schoep, Tobias, Shelat, Anang A., Stewart, Clinton F., Sullivan, Michael, Taylor, Michael D., Wainwright, Brandon, Walwyn, Thomas, Weiss, William A., Williamson, Dan, Gajjar, Amar
Published in Acta neuropathologica

Can sacral development as a marker for caudal regression help identify associated urologic anomalies in patients with anorectal malformation?

by Vilanova-Sanchez, Alejandra, Reck, Carlos A., Sebastião, Yuri V., Fuchs, Molly, Halleran, Devin R., Weaver, Laura, Gregory Bates, D., Gasior, Alessandra C., Maloof, Tassiana, Hoover, Erin J., Jaggers, Jordan, Gagnon, Renae, Ching, Christina C., Dajusta, Daniel, Jayanthi, Venkata R., Levitt, Marc A., Wood, Richard J.
Published in Journal of pediatric surgery

De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype

by Pena, Loren D.M., Hempel, Maja, McLaughlin, Heather M., Cho, Megan, Stong, Nicholas, Shuss, Christine M., Burrage, Lindsay C., Dhar, Shweta U., Emrick, Lisa T., Graham, Brett H., Lalani, Seema R., Lewis, Richard A., Posey, Jennifer E., Hanchard, Neil A., Mercedes, Alejandro E., Wangler, Michael F., Muzny, Donna M., Ward, Patricia A., Ramoni, Rachel B., McCray, Alexa T., Mazur, Paul, Splinter, Kimberly, Esteves, Cecilia, Jiang, Yong-hui, Pena, Loren D.M., McConkie-Rosell, Allyn, Schoch, Kelly, Spillmann, Rebecca C., Goldstein, David B., Loscalzo, Joseph, Rodan, Lance H., Walsh, Chris A., Cooper, Cynthia M., Donnell-Fink, Laurel A., Krieg, Elizabeth L., Lincoln, Sharyn A., Worthey, Elizabeth A., Lazar, Joe, Handley, Lori H., Newberry, J. Scott, Schroeder, Molly C., Brown, Donna M., Levy, Shawn E., Dorset, Dan C., Jones, Angela L., Manolio, Teri A., Wise, Anastasia L., Eckstein, David J., Krasnewich, Donna M., Loomis, Carson R., Iglesias, Brenda, Martin, Casey, Koeller, David M., Ashley, Euan A., Zornio, Patricia A., Nelson, Stan F., Palmer, Christina G.S., Allard, Patrick, Dell Angelica, Esteban C., Lee, Hane, Papp, Jeanette C., Dorrani, Naghmeh, Draper, David D., Estwick, Tyra, Gahl, William A., Gartner, Valerie, Godfrey, Rena A., Goheen, Mitchell, Johnston, Jean M., Latham, Lea, Macnamara, Ellen F., Maduro, Valerie V., Malicdan, May V., McCarty, Alexandra J., Murphy, Jennifer L., Novacic, Donna, Pusey, Barbara N., Sadozai, Sarah, Schaffer, Katherine E., Sharma, Prashant, Soldatos, Ariane G., Tifft, Cynthia J., Tolman, Nathanial J., Toro, Camilo, Wahl, Colleen E., Weech, Alec A., Yu, Guoyun, Hamid, Rizwan, Bellet, Jane S., Keels, Martha Ann, El-Dairi, Maysantoine, Stumpel, Constance T.R.M., Klinkenberg, Sylvia, Oberndorff, Karin, Petrovski, Slavé, Kuismin, Outi, Korpi-Heikkilä, Satu, Kurki, Mitja I., Hoischen, Alexander, Goldstein, David B.
Published in American journal of human genetics