Frequency of JAK2 and MPL Mutation in BCR/ABL Negative Myelofibrosis in KPK von Ayesha Gul, Sheeba Ishtiaq, Hina Umair, Memoona Rasheed, Ayesha Gul, Sheeba Ishtiaq, Hina Umair, Memoona Rasheed

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Exome sequencing identifies novel and known mutations in families with intellectual disability von Rasheed, Memoona, Khan, Valeed, Harripaul, Ricardo, Siddiqui, Maimoona, Malik, Madiha Amin, Ullah, Zahid, Zahid, Muhammad, Vincent, John B., Ansar, Muhammad

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Next Generation Sequencing as an Emerging Technology in Rare Disease Genetics von Memoona Rasheed

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Genomic Analysis Identifies Risk Factors in Restless Legs Syndrome von Akçimen, Fulya, Chia, Ruth, Saez‐Atienzar, Sara, Ruffo, Paola, Rasheed, Memoona, Ross, Jay P., Liao, Calwing, Ray, Anindita, Dion, Patrick A., Scholz, Sonja W., Rouleau, Guy A., Traynor, Bryan J.

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Homozygous missense variant in POPDC3 causes recessive limb‐girdle muscular dystrophy type 26 von Ullah, Anwar, Lin, Zhaohan, Younus, Muhammad, Shafiq, Sarfraz, Khan, Shazia, Rasheed, Memoona, Mahmood, Arif, Alqosaibi, Amany I., Alshehri, Mohammed Ali, Khan, Amjad, Umair, Muhammad

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Novel candidate genes and variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability von Santos-Cortez, Regie Lyn P., Khan, Valeed, Khan, Falak Sher, Mughal, Zaib-un-Nisa, Chakchouk, Imen, Lee, Kwanghyuk, Rasheed, Memoona, Hamza, Rifat, Acharya, Anushree, Ullah, Ehsan, Saqib, Muhammad Arif Nadeem, Abbe, Izoduwa, Ali, Ghazanfar, Hassan, Muhammad Jawad, Khan, Saadullah, Azeem, Zahid, Ullah, Irfan, Bamshad, Michael J., Nickerson, Deborah A., Schrauwen, Isabelle, Ahmad, Wasim, Ansar, Muhammad, Leal, Suzanne M.

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Biallelic missense variants in ZBTB11 can cause intellectual disability in humans von Fattahi, Zohreh, Sheikh, Taimoor I, Musante, Luciana, Rasheed, Memoona, Taskiran, Ibrahim Ihsan, Harripaul, Ricardo, Hu, Hao, Kazeminasab, Somayeh, Alam, Muhammad Rizwan, Hosseini, Masoumeh, Larti, Farzaneh, Ghaderi, Zhila, Celik, Arzu, Ayub, Muhammad, Ansar, Muhammad, Haddadi, Mohammad, Wienker, Thomas F, Ropers, Hans Hilger, Kahrizi, Kimia, Vincent, John B, Najmabadi, Hossein

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Homozygous Missense Variant in the N-Terminal Region of ANK3 Gene Is Associated with Developmental Delay, Seizures, Speech Abnormality, and Aggressive Behavior von Younus, Muhammad, Rasheed, Memoona, Lin, Zhaohan, Asiri, Saeed A., Almazni, Ibrahim A., Alshehri, Mohammed Ali, Shafiq, Sarfraz, Iqbal, Imran, Khan, Amjad, Ullah, Hanif, Umair, Muhammad, Waqas, Ahmed

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Structural variants in Lewy body dementia and frontotemporal dementia spectrum von Kaivola, Karri, Chia, Ruth, Ding, Jinhui, Rasheed, Memoona, Fujita, Masashi, Menon, Vilas, Walton, Ronald L., Collins, Ryan, Billingsley, Kimberley, Brand, Harrison, Talkowski, Michael, Zhao, Xuefang, Dewan, Ramita, Ray, Anindita K, Solaiman, Sultana, Jerez, Pilar Alvarez, Malik, Laksh, Dawson, Ted M, Rosenthal, Liana, Albert, Marilyn S., Pletnikova, Olga, Troncoso, Juan C, Masellis, Mario, Keith, Julia, Black, Sandra E., Ferrucci, Luigi, Resnick, Susan M., Tanaka, Toshiko, Topol, Eric, Torkamani, Ali, Tienari, Pentti, Foroud, Tatiana M., Ghetti, Bernardino Francesco, Landers, John E, Ryten, Mina, Morris, Huw R, Hardy, John A., Mazzini, Letizia, D'Alfonso, Sandra, Moglia, Cristina, Calvo, Andrea, Serrano, Geidy E, Beach, Thomas G, Ferman, Tanis J, Graff‐Radford, Neill R, Boeve, Brad F., Wszolek, Zbigniew, Dickson, Dennis W., Chio, Adriano, Bennett, David A. A, De Jager, Philip L, Ross, Owen A., Dalgard, Clifton L., Gibbs, J. Raphael, Traynor, Bryan J, Scholz, Sonja W

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Biallelic missense variants in ZBTB11 can cause intellectual disability in humans von Fattahi, Zohreh, Sheikh, Taimoor I, Musante, Luciana, Rasheed, Memoona, Taskiran, Ibrahim Ihsan, Harripaul, Ricardo, Hu, Hao, Kazeminasab, Somayeh, Alam, Muhammad Rizwan, Hosseini, Masoumeh, Larti, Farzaneh, Ghaderi, Zhila, Celik, Arzu, Ayub, Muhammad, Ansar, Muhammad, Haddadi, Mohammad, Wienker, Thomas F, Ropers, Hans Hilger, Kahrizi, Kimia, Vincent, John B, Najmabadi, Hossein

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Genome-wide structural variant analysis identifies risk loci for non-Alzheimer’s dementias von Kaivola, Karri, Ding, Jinhui, Fujita, Masashi, Menon, Vilas, Walton, Ronald L., Collins, Ryan L., Billingsley, Kimberley, Talkowski, Michael, Dewan, Ramita, Ray, Anindita, Alvarez Jerez, Pilar, Albert, Marilyn S., Resnick, Susan M., Sukumar, Gauthaman, Lott, Nathaniel, Tuck, Meila, Bacikova, Dagmar, Adeleye, Adelani, Black, Sandra E., Gan-Or, Ziv, Rogaeva, Ekaterina, Lesage, Suzanne, Xiromerisiou, Georgia, Calvo, Andrea, Canosa, Antonio, Logroscino, Giancarlo, Clarimon, Jordi, Brett, Francesca, Aarsland, Dag, Al-Sarraj, Safa, Attems, Johannes, McKeith, Ian G., Morris, Christopher M., Morris, Huw R., Pickering-Brown, Stuart, Ryten, Mina, Thomas, Alan J., Troakes, Claire, Albert, Marilyn S., Barrett, Matthew J., Bennett, David A., Dickson, Dennis W., Faber, Kelley, Ferrucci, Luigi, Flanagan, Margaret E., Foroud, Tatiana M., Ghetti, Bernardino, Gibbs, J. Raphael, Goate, Alison, Graff-Radford, Neill R., Kaufmann, Horacio, Kukull, Walter A., Lopez, Grisel, Mao, Qinwen, Masliah, Eliezer, Pletnikova, Olga, Renton, Alan E., Ross, Owen A., Serrano, Geidy E., Sidransky, Ellen, Tayebi, Nahid, Torkamani, Ali, Wszolek, Zbigniew K., Broach, James, Drory, Vivian E., Dunckley, Travis L., Gerhard, Glenn, Gibson, Summer B., Heiman-Patterson, Terry D., Jansson, Lilja, Kwan, Justin, Laaksovirta, Hannu, Landers, John E., Landi, Francesco, Le Ber, Isabelle, Lumbroso, Serge, MacGowan, Daniel J.L., Maragakis, Nicholas J., Myllykangas, Liisa, Orrell, Richard W., Pamphlett, Roger, Pulst, Stefan M., Rothstein, Jeffrey D., Shaw, Pamela J., Sidle, Katie C., Simmons, Zachary, Stone, David J., Van Deerlin, Vivianna M., Van Den Bosch, Ludo, Topol, Eric, Ghetti, Bernardino, Landers, John E., Morris, Huw R., Hardy, John A., Moglia, Cristina, Calvo, Andrea, Beach, Thomas G., Ferman, Tanis, Bennett, David A., Traynor, Bryan J.

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Additional file 1 of Exome sequencing identifies novel and known mutations in families with intellectual disability von Rasheed, Memoona, Khan, Valeed, Harripaul, Ricardo, Siddiqui, Maimoona, Malik, Madiha Amin, Ullah, Zahid, Zahid, Muhammad, Vincent, John B., Ansar, Muhammad

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The implication of CRISPR/Cas9 genome editing technology in combating human oncoviruses von Gilani, Usman, Shaukat, Memoona, Rasheed, Arisha, Shahid, Mehak, Tasneem, Fareeda, Arshad, Muhammad, Rashid, Naeem, Shahzad, Naveed

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Toxicological effects of zinc oxide nanoparticles on hemato-biochemical profile of common carp (Cyprinus carpio) von Rasheed, Abdul, Javed Iqbal, Khalid, Safdar, Aleena, Nasir, Amar, Jabeen, Raheela, sami, Amtul, Tara, Nain, Ali, Sadaqat, Zeeshan, Muhammad, Abbas, Shaista, Aun Muhammad, Sayyed, Pervaiz, Afsah, Adil, Memoona, Han, Jilong, Ali, Daoud, Almarzoug, Mohammed H.A.

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Intraoperative Neurophysiological Monitoring During Resection of Posterior Fossa Lesions von Ejaz, Memoona, Khan, Habibullah, Mushtaq, Junaid, Safdar, Kaleem, Bangash, Khurshid Ali, Farooq, Umer, Tashfeen, Ahmed, Ahmed, Ali, Ahmed, Zeeshan, Rasheed, Asif, Hashmi, Fasih

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Prevalence of carpal tunnel syndrome in computer operators of Peshawar von Memoona Bibi, Bilal Khan, Sana Rasheed Ahmad, Asmat Hassanat, Romaisa Ijaz, Hazrat Usman

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Nutritional Imbalance, Toxicology and Deficiency Potential of Livestock von Ouf, Salama A., Rasheed, Jahanzaib, Ahmad, Kafeel, Khan, Zafar Iqbal, Wajid, Kinza, Nadeem, Muhammad, Tehreem, Shahwana, Abbas, Tasawar, Bashir, Humayun, Ashfaq, Asma, Munir, Mudasra, Malik, Ifra Saleem, Memoona, Hafsa, Noorka, Ijaz Rasool, Mahpara, Shahzadi, Mohamed, Osama B.

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