Clinical impact of copy number variation analysis using high-resolution microarray technologies: advantages, limitations and concerns

por Coughlin, Curtis R, Scharer, Gunter H, Shaikh, Tamim H
Publicado 2012

Impact of an age, kidney and liver function adjusted sedation protocol in critically ill patients

por Haddad, S, Tamim, H, Gonzales, C, Rishu, A, Deeb, A, Arabi, Y
Publicado 2013

Integration of Evidence Based Medicine into a Medical Curriculum

por Tamim, H M, Ferwana, M, Al Banyan, E, Al Alwan, I, Hajeer, AH
Publicado 2009

Comparing febrile children presenting on and off antibiotics to the emergency department: a retrospective cohort study

por Sawaya, R. D., El Zahran, T., Mrad, S., Abdul Massih, C., Shaya, S., Makki, M., Tamim, H., Majdalani, M.
Publicado 2020

Abnormal expression of GABA(A) receptor subunits and hypomotility upon loss of gabra1 in zebrafish

por Reyes-Nava, Nayeli G., Yu, Hung-Chun, Coughlin, Curtis R., Shaikh, Tamim H., Quintana, Anita M.
Publicado 2020

22q11.2 Low Copy Repeats Expanded in the Human Lineage

por Vervoort, Lisanne, Dierckxsens, Nicolas, Pereboom, Zjef, Capozzi, Oronzo, Rocchi, Mariano, Shaikh, Tamim H., Vermeesch, Joris R.
Publicado 2021

Profile, outcomes, and predictors of mortality of abdomino-pelvic trauma patients in a tertiary ICU in Saudi Arabia

por Haddad, S, Youssef, Z, Azzam, S, Aldawood, A, Al-Zahrani, A, Al-Zamel, H, Tamim, H, Deeb, A, Arabi, Y
Publicado 2014

Evaluating Familial Essential Tremor with Novel Genetic Approaches: Is it a Genotyping or Phenotyping Issue?

por Gonzalez-Alegre, Pedro, Di Paola, Jorge, Wang, Kai, Fabbro, Shay, Yu, Hung-Chun, Shaikh, Tamim H., Darbro, Benjamin W., Bassuk, Alexander G.
Publicado 2014

CNV Workshop: an integrated platform for high-throughput copy number variation discovery and clinical diagnostics

por Gai, Xiaowu, Perin, Juan C, Murphy, Kevin, O'Hara, Ryan, D'arcy, Monica, Wenocur, Adam, Xie, Hongbo M, Rappaport, Eric F, Shaikh, Tamim H, White, Peter S
Publicado 2010

Genome-wide analysis of copy number variants and normal facial variation in a large cohort of Bantu Africans

por Null, Megan, Yilmaz, Feyza, Astling, David, Yu, Hung-Chun, Cole, Joanne B., Hallgrímsson, Benedikt, Santorico, Stephanie A., Spritz, Richard A., Shaikh, Tamim H., Hendricks, Audrey E.
Publicado 2021

Discovery of a potentially deleterious variant in TMEM87B in a patient with a hemizygous 2q13 microdeletion suggests a recessive condition characterized by congenital heart disease...

por Yu, Hung-Chun, Coughlin, Curtis R., Geiger, Elizabeth A., Salvador, Blake J., Elias, Ellen R., Cavanaugh, Jean L., Chatfield, Kathryn C., Miyamoto, Shelley D., Shaikh, Tamim H.
Publicado 2016

Genome-wide copy number variations in a large cohort of bantu African children

por Yilmaz, Feyza, Null, Megan, Astling, David, Yu, Hung-Chun, Cole, Joanne, Santorico, Stephanie A., Hallgrimsson, Benedikt, Manyama, Mange, Spritz, Richard A., Hendricks, Audrey E., Shaikh, Tamim H.
Publicado 2021

High level of complexity and global diversity of the 3q29 locus revealed by optical mapping and long-read sequencing

por Yilmaz, Feyza, Gurusamy, Umamaheswaran, Mosley, Trenell J., Hallast, Pille, Kim, Kwondo, Mostovoy, Yulia, Purcell, Ryan H., Shaikh, Tamim H., Zwick, Michael E., Kwok, Pui-Yan, Lee, Charles, Mulle, Jennifer G.
Publicado 2023

Assessing climate-induced agricultural vulnerable coastal communities of Bangladesh using machine learning techniques

por Jakariya, Md., Alam, Md. Sajadul, Rahman, Md. Abir, Ahmed, Silvia, Elahi, M.M. Lutfe, Khan, Abu Mohammad Shabbir, Saad, Saman, Tamim, H.M., Ishtiak, Taoseef, Sayem, Sheikh Mohammad, Ali, Mirza Shawkat, Akter, Dilruba
Publicado 2020

The 22q11 low copy repeats are characterized by unprecedented size and structural variability

por Demaerel, Wolfram, Mostovoy, Yulia, Yilmaz, Feyza, Vervoort, Lisanne, Pastor, Steven, Hestand, Matthew S., Swillen, Ann, Vergaelen, Elfi, Geiger, Elizabeth A., Coughlin, Curtis R., Chow, Stephen K., McDonald-McGinn, Donna, Morrow, Bernice, Kwok, Pui-Yan, Xiao, Ming, Emanuel, Beverly S., Shaikh, Tamim H., Vermeesch, Joris R.
Publicado 2019

500P The impact of COVID-19 on the management and outcome of oncology patients: The results of the Middle East and North African (MENA) COVID-19 and Cancer Registry (MCCR)

por Jazieh, A.R., Abdel-Razeq, H., Köksoy, E.B., Bounedjar, A., Tafayli, A., Tashkandi, E., Jastaniah, W., Ansari, J., Alorabi, M.O., Darwish, A.D., Rabea, A., Alolayan, A.A.M., Ibnshamsa, F., Errihani, H., Alkaiyat, M., Garrett-Mayer, E., Bruinooge, S.S., Hussain, F., Tamim, H., AlKattan, K.
Publicado 2022

Genomic and Genic Deletions of the FOX Gene Cluster on 16q24.1 and Inactivating Mutations of FOXF1 Cause Alveolar Capillary Dysplasia and Other Malformations

por Stankiewicz, Paweł, Sen, Partha, Bhatt, Samarth S., Storer, Mekayla, Xia, Zhilian, Bejjani, Bassem A., Ou, Zhishuo, Wiszniewska, Joanna, Driscoll, Daniel J., Bolivar, Juan, Bauer, Mislen, Zackai, Elaine H., McDonald-McGinn, Donna, Nowaczyk, Małgorzata M.J., Murray, Mitzi, Shaikh, Tamim H., Martin, Vicki, Tyreman, Matthew, Simonic, Ingrid, Willatt, Lionel, Paterson, Joan, Mehta, Sarju, Rajan, Diana, Fitzgerald, Tomas, Gribble, Susan, Prigmore, Elena, Patel, Ankita, Shaffer, Lisa G., Carter, Nigel P., Cheung, Sau Wai, Langston, Claire, Shaw-Smith, Charles
Publicado 2009

A recurrent 16p12.1 microdeletion suggests a two-hit model for severe developmental delay

por Girirajan, Santhosh, Rosenfeld, Jill A., Cooper, Gregory M., Antonacci, Francesca, Siswara, Priscillia, Itsara, Andy, Vives, Laura, Walsh, Tom, McCarthy, Shane E., Baker, Carl, Mefford, Heather C., Kidd, Jeffrey M., Browning, Sharon R., Browning, Brian L., Dickel, Diane E., Levy, Deborah L., Ballif, Blake C., Platky, Kathryn, Farber, Darren M., Gowans, Gordon C., Wetherbee, Jessica J., Asamoah, Alexander, Weaver, David D., Mark, Paul R., Dickerson, Jennifer, Garg, Bhuwan P., Ellingwood, Sara A., Smith, Rosemarie, Banks, Valerie C., Smith, Wendy, McDonald, Marie T., Hoo, Joe J., French, Beatrice N., Hudson, Cindy, Johnson, John P., Ozmore, Jillian R., Moeschler, John B., Surti, Urvashi, Escobar, Luis F., El-Kechen, Dima, Gorski, Jerome L., Kussman, Jennifer, Salbert, Bonnie, Lacassie, Yves, Biser, Alisha, McDonald-McGinn, Donna M., Zackai, Elaine H., Deardorff, Matthew A., Shaikh, Tamim H., Haan, Eric, Friend, Kathryn L., Fichera, Marco, Romano, Corrado, Gécz, Jozef, deLisi, Lynn E., Sebat, Jonathan, King, Mary-Claire, Shaffer, Lisa G., Eichler, Evan E.
Publicado 2010

Microduplications of 16p11.2 are Associated with Schizophrenia

por McCarthy, Shane, Makarov, Vladimir, Kirov, George, Addington, Anjene, McClellan, Jon, Yoon, Seungtai, Perkins, Dianna, Dickel, Diane E., Kusenda, Mary, Krastoshevsky, Olga, Krause, Verena, Kumar, Ravinesh A., Grozeva, Detelina, Malhotra, Dheeraj, Walsh, Tom, Zackai, Elaine H., Kaplan, Paige, Ganesh, Jaya, Krantz, Ian D., Spinner, Nancy B., Roccanova, Patricia, Bhandari, Abhishek, Pavon, Kevin, Lakshmi, B., Leotta, Anthony, Kendall, Jude, Lee, Yoon-ha, Vacic, Vladimir, Gary, Sydney, Iakoucheva, Lilia, Crow, Timothy J., Christian, Susan L., Lieberman, Jeffrey, Stroup, Scott, Lehtimäki, Terho, Puura, Kaija, Haldeman-Englert, Chad, Pearl, Justin, Goodell, Meredith, Willour, Virginia L., DeRosse, Pamela, Steele, Jo, Kassem, Layla, Wolff, Jessica, Chitkara, Nisha, McMahon, Francis J., Malhotra, Anil K., Potash, James B., Schulze, Thomas G., Nöthen, Markus M., Cichon, Sven, Rietschel, Marcella, Leibenluft, Ellen, Kustanovich, Vlad, Lajonchere, Clara M., Sutcliffe, James S., Skuse, David, Gill, Michael, Gallagher, Louise, Mendell, Nancy R., Craddock, Nick, Owen, Michael J., O’Donovan, Michael C., Shaikh, Tamim H., Susser, Ezra, DeLisi, Lynn E., Sullivan, Patrick F., Deutsch, Curtis K., Rapoport, Judith, Levy, Deborah L., King, Mary-Claire, Sebat, Jonathan
Publicado 2009