未登录Determining Cost-Optimal Next-Generation Sequencing Panels for Rare Disease and Pharmacogenomics Testing
Katragadda, Shanmukh; Hall, Taryn O.; Bettadapura, Radhakrishna; Dalton, Joline C.; Ganapathy, Aparna; Ghana, Pallavi; Hariharan, Ramesh; Janakiraman, Anand; Kotha, Kumar B. V. S. S. P.; Manjunath, Ashwini; Mannan, Ashraf U.; Niveditha, M. S.; Saraf, Shradha; Tzeng, Kathy T. H.; Veeramachaneni, Vamsi
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收藏Genetic Counseling, Testing, and Management of HBOC in India: An Expert Consensus Document from Indian Society of Medical and Pediatric Oncology
Malhotra, Hemant; Kowtal, Pradnya; Mehra, Nikita; Pramank, Raja; Sarin, Rajiv; Rajkumar, Thangarajan; Gupta, Sudeep; Bapna, Ajay; Bhattacharyya, Gouri Shankar; Gupta, Sabhyata; Maheshwari, Amita; Mannan, Ashraf U.; Kundur, Ravindra Reddy; Sekhon, Rupinder; Singhal, Manish; Smruti, B. K.; Somashekhar, S. P.; Suryavanshi, Moushumi; Verma, Amit
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收藏Screening of over 1000 Indian patients with breast and/or ovarian cancer with a multi-gene panel: prevalence of BRCA1/2 and non-BRCA mutations
Singh, Jaya; Thota, Nishita; Singh, Suhasini; Padhi, Shila; Mohan, Puja; Deshwal, Shivani; Sur, Soumit; Ghosh, Mithua; Agarwal, Amit; Sarin, Ramesh; Ahmed, Rosina; Almel, Sachin; Chakraborti, Basumita; Raina, Vinod; DadiReddy, Praveen K.; Smruti, B. K.; Rajappa, Senthil; Dodagoudar, Chandragouda; Aggarwal, Shyam; Singhal, Manish; Joshi, Ashish; Kumar, Rajeev; Kumar, Ajai; Mishra, Deepak K.; Arora, Neeraj; Karaba, Aarati; Sankaran, Satish; Katragadda, Shanmukh; Ghosh, Arunabha; Veeramachaneni, Vamsi; Hariharan, Ramesh; Mannan, Ashraf U.
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收藏Analytical and technical validation of a cost-effective diagnostic test for BRCA1, BRCA2 and TP53
Sen, Manimala; Agrawal, Pooja; Vittal, Vikram P.; Ghosh, Mithua; Sheela, M. L.; Vishwanath, Divya; Kumari, Kiran; Swetha, N. S. N.; Pathak, Vaibhavi; Deshpande, Gouri; Mannan, Ashraf; Gadkari, Rupali; Kapoor, Suman; Yadhav, Jamuna; Yousuff, Mohammed; Sankaran, Satish; Hariharan, Ramesh; Ramamoorthy, Preveen; Subramanian, Kalyanasundaram; Gupta, Vaijayanti
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收藏Mild expression differences of MECP2 influencing aggressive social behavior
Tantra, Martesa; Hammer, Christian; Kaestner, Anne; Dahm, Liane; Begemann, Martin; Bodda, Chiranjeevi; Hammerschmidt, Kurt; Giegling, Ina; Stepniak, Beata; Venzor, Aracely Castillo; Konte, Bettina; Erbaba, Begun; Hartmann, Annette; Tarami, Asieh; Schulz-Schaeffer, Walter; Rujescu, Dan; Mannan, Ashraf U.; Ehrenreich, Hannelore
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收藏Mild Overexpression of Mecp2 in Mice Causes a Higher Susceptibility toward Seizures
Bodda, Chiranjeevi; Tantra, Martesa; Mollajew, Rustam; Arunachalam, Jayamuruga P.; Laccone, Franco A.; Can, Karolina; Rosenberger, Albert; Mironov, Sergej L.; Ehrenreich, Hannelore; Mannan, Ashraf U.
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收藏Expansion of mutation spectrum, determination of mutation cluster regions and predictive structural classification of SPAST mutations in hereditary spastic paraplegia (vol 17, pg 187, 2009)
Shoukier, Moneef; Neesen, Juergen; Sauter, Simone M.; Argyriou, Loukas; Doerwald, Nadine; Pantakani, D. V. Krishna; Mannan, Ashraf U.
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收藏ZFYVE27 (SPG33), a novel spastin-binding protein, is mutated in hereditary spastic paraplegia
Mannan, Ashraf U.; Krawen, Philip; Sauter, Simone M.; Boehm, Johann; Chronowska, Agnieszka; Paulus, Walter; Neesen, Juergen; Engel, Wolfgang
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