Spatio-temporal hybrid neural networks reduce erroneous human “judgement calls” in the diagnosis of Takotsubo syndrome von Zaman, Fahim, Ponnapureddy, Rakesh, Wang, Yi Grace, Chang, Amanda, Cadaret, Linda M, Abdelhamid, Ahmed, Roy, Shubha D, Makan, Majesh, Zhou, Ruihai, Jayanna, Manju B, Gnall, Eric, Dai, Xuming, Singh, Avneet, Zheng, Jingsheng, Boppana, Venkata S, Wang, Feng, Singh, Pahul, Wu, Xiaodong, Liu, Kan

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ADULT BONE MARROW CELL THERAPY IMPROVES LEFT VENTRICULAR FUNCTION IN PATIENTS WITH ISCHEMIC HEART DISEASE: A META-ANALYSIS OF RANDOMIZED CONTROLLED TRIALS UTILIZING CARDIAC MAGNETI... von Samanta, Anweshan, Afzal, Muhammad, Cantilena, Amy, Samanta, Ipsita, Taduru, Siva Sagar, Roy, Shubha D., Dawn, Buddhadeb

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“Takotsubo effect” in patients with ST segment elevation myocardial infarction von Lei, Juan, Chen, Jian, Dogra, Megha, Gebska, Milena A, Shetty, Suchith, Ponnapureddy, Rakesh, Roy, Shubha D, Wang, Jingfeng, Liu, Kan

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Mutations in DZIP1L, which encodes a ciliary-transition-zone protein, cause autosomal recessive polycystic kidney disease von Lu, Hao, Galeano, Maria C Rondón, Ott, Elisabeth, Kaeslin, Geraldine, Kausalya, P Jaya, Kramer, Carina, Ortiz-Brüchle, Nadina, Hilger, Nadescha, Metzis, Vicki, Hiersche, Milan, Tay, Shang Yew, Tunningley, Robert, Vij, Shubha, Courtney, Andrew D, Whittle, Belinda, Wühl, Elke, Vester, Udo, Hartleben, Björn, Neuber, Steffen, Frank, Valeska, Little, Melissa H, Epting, Daniel, Papathanasiou, Peter, Perkins, Andrew C, Wright, Graham D, Hunziker, Walter, Gee, Heon Yung, Otto, Edgar A, Zerres, Klaus, Hildebrandt, Friedhelm, Roy, Sudipto, Wicking, Carol, Bergmann, Carsten

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CARDIAC TAMPONADE DUE TO A RARE CAUSE OF PURULENT PERICARDITIS MIMICKING LYMPHOMA von Statz, Giselle M., Soltys, Matthew D., MacFarlane, Donald, Roy, Shubha Deep, Gebska, Milena A.

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LHX2 Interacts with the NuRD Complex and Regulates Cortical Neuron Subtype Determinants Fezf2 and Sox11 von Muralidharan, Bhavana, Khatri, Zeba, Maheshwari, Upasana, Gupta, Ritika, Roy, Basabdatta, Pradhan, Saurabh J, Karmodiya, Krishanpal, Padmanabhan, Hari, Shetty, Ashwin S, Balaji, Chinthapalli, Kolthur-Seetharam, Ullas, Macklis, Jeffrey D, Galande, Sanjeev, Tole, Shubha

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Ocean color algorithm for the retrieval of the particle size distribution and carbon-based phytoplankton size classes using a two-component coated-sphere backscattering model von Kostadinov, Tihomir S, Robertson Lain, Lisl, Kong, Christina Eunjin, Zhang, Xiaodong, Maritorena, Stéphane, Bernard, Stewart, Loisel, Hubert, Jorge, Daniel S. F, Kochetkova, Ekaterina, Roy, Shovonlal, Jonsson, Bror, Martinez-Vicente, Victor, Sathyendranath, Shubha

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Development of human protein reference database as an initial platform for approaching systems biology in humans von Peri, Suraj, Navarro, J Daniel, Amanchy, Ramars, Kristiansen, Troels Z, Jonnalagadda, Chandra Kiran, Surendranath, Vineeth, Niranjan, Vidya, Muthusamy, Babylakshmi, Gandhi, T K B, Gronborg, Mads, Ibarrola, Nieves, Deshpande, Nandan, Shanker, K, Shivashankar, H N, Rashmi, B P, Ramya, M A, Zhao, Zhixing, Chandrika, K N, Padma, N, Harsha, H C, Yatish, A J, Kavitha, M P, Menezes, Minal, Choudhury, Dipanwita Roy, Suresh, Shubha, Ghosh, Neelanjana, Saravana, R, Chandran, Sreenath, Krishna, Subhalakshmi, Joy, Mary, Anand, Sanjeev K, Madavan, V, Joseph, Ansamma, Wong, Guang W, Schiemann, William P, Constantinescu, Stefan N, Huang, Lily, Khosravi-Far, Roya, Steen, Hanno, Tewari, Muneesh, Ghaffari, Saghi, Blobe, Gerard C, Dang, Chi V, Garcia, Joe G N, Pevsner, Jonathan, Jensen, Ole N, Roepstorff, Peter, Deshpande, Krishna S, Chinnaiyan, Arul M, Hamosh, Ada, Chakravarti, Aravinda, Pandey, Akhilesh

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Human protein reference database as a discovery resource for proteomics von Peri, Suraj, Navarro, J. Daniel, Kristiansen, Troels Z., Amanchy, Ramars, Surendranath, Vineeth, Muthusamy, Babylakshmi, Gandhi, T. K. B., Chandrika, K. N., Deshpande, Nandan, Suresh, Shubha, Rashmi, B. P., Shanker, K., Padma, N., Niranjan, Vidya, Harsha, H. C., Talreja, Naveen, Vrushabendra, B. M., Ramya, M. A., Yatish, A. J., Joy, Mary, Shivashankar, H. N., Kavitha, M. P., Menezes, Minal, Choudhury, Dipanwita Roy, Ghosh, Neelanjana, Saravana, R., Chandran, Sreenath, Mohan, Sujatha, Jonnalagadda, Chandra Kiran, Prasad, C. K., Kumar‐Sinha, Chandan, Deshpande, Krishna S., Pandey, Akhilesh

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LHX2 Interacts with the NuRD Complex and Regulates Cortical Neuron Subtype Determinants Fezf2 and Sox11 von Muralidharan, Bhavana, Khatri, Zeba, Maheshwari, Upasana, Gupta, Ritika, Roy, Basabdatta, Pradhan, Saurabh J., Karmodiya, Krishanpal, Padmanabhan, Hari, Shetty, Ashwin S., Balaji, Chinthapalli, Kolthur-Seetharam, Ullas, Macklis, Jeffrey D., Galande, Sanjeev, Tole, Shubha

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LHX2 Interacts with the NuRD Complex and Regulates Cortical Neuron Subtype Determinants Fezf2 and Sox11 von Muralidharan, Bhavana, Khatri, Zeba, Maheshwari, Upasana, Gupta, Ritika, Roy, Basabdatta, Pradhan, Saurabh J, Karmodiya, Krishanpal, Padmanabhan, Hari, Shetty, Ashwin S, Balaji, Chinthapalli, Kolthur-Seetharam, Ullas, Macklis, Jeffrey D, Galande, Sanjeev, Tole, Shubha

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Mutations in DZIP1L, which encodes a ciliary-transition-zone protein, cause autosomal recessive polycystic kidney disease von Lu, Hao, Rondón Galeano, Maria C, Ott, Elisabeth, Kaeslin, Geraldine, Kausalya, P Jaya, Kramer, Carina, Ortiz-Brüchle, Nadina, Hilger, Nadescha, Metzis, Vicki, Hiersche, Milan, Tay, Shang Yew, Tunningley, Robert, Vij, Shubha, Courtney, Andrew D, Whittle, Belinda, Wühl, Elke, Vester, Udo, Hartleben, Björn, Neuber, Steffen, Frank, Valeska, Little, Melissa H, Epting, Daniel, Papathanasiou, Peter, Perkins, Andrew C, Wright, Graham D, Hunziker, Walter, Gee, Heon Yung, Otto, Edgar A, Zerres, Klaus, Hildebrandt, Friedhelm, Roy, Sudipto, Wicking, Carol, Bergmann, Carsten

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RPGRIP1L mutations are mainly associated with the cerebello-renal phenotype of Joubert syndrome-related disorders von Brancati, F, Travaglini, L, Zablocka, D, Boltshauser, E, Accorsi, P, Montagna, G, Silhavy, JL, Barrano, G, Bertini, E, Emma, F, Rigoli, L, Dallapiccola, B, Gleeson, JG, Valente, EM

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Possible role of male factors in recurrent pregnancy loss von Saxena, Pikee, Misro, M M, Roy, Somnath, Chopra, K, Sinha, D, Nandan, Deoki, Trivedi, Shubha Sagar

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A manually curated functional annotation of the human X chromosome von Pandey, Akhilesh, Harsha, H C, Suresh, Shubha, Amanchy, Ramars, Deshpande, Nandan, Shanker, K, Yatish, A J, Muthusamy, Babylakshmi, Vrushabendra, B M, Rashmi, B P, Chandrika, K N, Padma, N, Sharma, Salil, Badano, Jose L, Ramya, M A, Shivashankar, H N, Peri, Suraj, Choudhury, Dipanwita Roy, Kavitha, M P, Saravana, R, Niranjan, Vidya, Gandhi, T K B, Ghosh, Neelanjana, Chandran, Sreenath, Menezes, Minal, Joy, Mary, Mohan, S Sujatha, Katsanis, Nicholas, Deshpande, Krishna S, Raghothama, Chaerkady, Prasad, C K

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