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Ashraf U. Mannan

University of Gottingen

20H指数
64论文数
1.1K被引数
收录论文 12
发表时间
Determining Cost-Optimal Next-Generation Sequencing Panels for Rare Disease and Pharmacogenomics Testing
err2021-06-13
err4
errOAAI
errKatragadda, 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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Genetic Counseling, Testing, and Management of HBOC in India: An Expert Consensus Document from Indian Society of Medical and Pediatric Oncology
err2020-11-01
err12
errOAAI
errMalhotra, 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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Chronic Mucocutaneous Candidiasis in an Adolescent Boy Due to a Novel Mutation in TRAF3IP2
err2019-07-10
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PREAI
errBhattad, Sagar; Dinakar, Chitra; Pinnamaraju, Haneesha; Ganapathy, Aparna; Mannan, Ashraf
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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
err2018-02-22
err61
PREAI
errSingh, 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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Analytical and technical validation of a cost-effective diagnostic test for BRCA1, BRCA2 and TP53
err2015-08-01
err0
PREAI
errSen, 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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Mild expression differences of MECP2 influencing aggressive social behavior
err2014-03-20
err24
errOAAI
errTantra, 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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Mild Overexpression of Mecp2 in Mice Causes a Higher Susceptibility toward Seizures
err2013-07-01
err38
errOAAI
errBodda, 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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Functional Evaluation of Paraplegin Mutations by a Yeast Complementation Assay
err2010-01-01
err41
PREAI
errBonn, Florian; Pantakani, Krishna; Shoukier, Moneef; Langer, Thomas; Mannan, Ashraf U.
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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)
err2009-02-19
err1
errOAAI
errShoukier, Moneef; Neesen, Juergen; Sauter, Simone M.; Argyriou, Loukas; Doerwald, Nadine; Pantakani, D. V. Krishna; Mannan, Ashraf U.
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Expansion of mutation spectrum, determination of mutation cluster regions and predictive structural classification of SPAST mutations in hereditary spastic paraplegia
err2008-08-13
err76
errOAAI
errShoukier, Moneef; Neesen, Juergen; Sauter, Simone M.; Argyriou, Loukas; Doerwald, Nadine; Pantakani, D. V. Krishna; Mannan, Ashraf U.
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ZFYVE27 (SPG33), a novel spastin-binding protein, is mutated in hereditary spastic paraplegia
err2006-08-01
err134
errOAAI
errMannan, Ashraf U.; Krawen, Philip; Sauter, Simone M.; Boehm, Johann; Chronowska, Agnieszka; Paulus, Walter; Neesen, Juergen; Engel, Wolfgang
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