Response to Martignoni et al.

od Mannan, Ashraf U.
Wydane 2008

Synaptic Nuclear Envelope Protein 1 (SYNE 1) Ataxia with Amyotrophic Lateral Sclerosis-like Presentation: A Novel Synaptic Nuclear Envelope Protein 1 (SYNE 1) Gene Deletion Mutatio...

od Nadaf, Swaleha Nurulla, Chakor, Rahul T., Kothari, Kaumil V., Mannan, Ashraf U.
Wydane w Ann Indian Acad Neurol (2020)

Oligomerization of ZFYVE27 (Protrudin) Is Necessary to Promote Neurite Extension

od Pantakani, D. V. Krishna, Czyzewska, Marta M., Sikorska, Anna, Bodda, Chiranjeevi, Mannan, Ashraf U.
Wydane 2011

Genetic variants in post myocardial infarction patients presenting with electrical storm of unstable ventricular tachycardia

od Rangaraju, Advithi, Krishnan, Shuba, Aparna, G., Sankaran, Satish, Mannan, Ashraf U., Rao, B. Hygriv
Wydane w Indian Pacing Electrophysiol J (2018)

1q42.12q42.2 Deletion in a Child with Midline Defects and Hypoplasia of the Corpus Callosum

od Radha Rama Devi, Akella, Ganapathy, Aparna, Mannan, Ashraf U., Sabharanjak, Shefali, Naushad, Shaik M.
Wydane w Mol Syndromol (2019)

Expansion of mutation spectrum, determination of mutation cluster regions and predictive structural classification of SPAST mutations in hereditary spastic paraplegia

od Shoukier, Moneef, Neesen, Juergen, Sauter, Simone M, Argyriou, Loukas, Doerwald, Nadine, Pantakani, DV Krishna, Mannan, Ashraf U
Wydane 2009

Expansion of mutation spectrum, determination of mutation cluster regions and predictive structural classification of SPAST mutations in hereditary spastic paraplegia

od Shoukier, Moneef, Neesen, Juergen, Sauter, Simone M, Argyriou, Loukas, Doerwald, Nadine, Pantakani, DV Krishna, Mannan, Ashraf U
Wydane 2009

ZFYVE27 (SPG33), a Novel Spastin-Binding Protein, Is Mutated in Hereditary Spastic Paraplegia

od Mannan, Ashraf U., Krawen, Philip, Sauter, Simone M., Boehm, Johann, Chronowska, Agnieszka, Paulus, Walter, Neesen, Juergen, Engel, Wolfgang
Wydane 2006

Sall1, Sall2, and Sall4 Are Required for Neural Tube Closure in Mice

od Böhm, Johann, Buck, Anja, Borozdin, Wiktor, Mannan, Ashraf U., Matysiak-Scholze, Uta, Adham, Ibrahim, Schulz-Schaeffer, Walter, Floss, Thomas, Wurst, Wolfgang, Kohlhase, Jürgen, Barrionuevo, Francisco
Wydane 2008

Next-generation sequencing-based method shows increased mutation detection sensitivity in an Indian retinoblastoma cohort

od Singh, Jaya, Mishra, Avshesh, Pandian, Arunachalam Jayamuruga, Mallipatna, Ashwin C., Khetan, Vikas, Sripriya, S., Kapoor, Suman, Agarwal, Smita, Sankaran, Satish, Katragadda, Shanmukh, Veeramachaneni, Vamsi, Hariharan, Ramesh, Subramanian, Kalyanasundaram, Mannan, Ashraf U.
Wydane w Mol Vis (2016)

Mild expression differences of MECP2 influencing aggressive social behavior

od Tantra, Martesa, Hammer, Christian, Kästner, Anne, Dahm, Liane, Begemann, Martin, Bodda, Chiranjeevi, Hammerschmidt, Kurt, Giegling, Ina, Stepniak, Beata, Castillo Venzor, Aracely, Konte, Bettina, Erbaba, Begun, Hartmann, Annette, Tarami, Asieh, Schulz-Schaeffer, Walter, Rujescu, Dan, Mannan, Ashraf U, Ehrenreich, Hannelore
Wydane 2014

Genetic Counseling, Testing, and Management of HBOC in India: An Expert Consensus Document from Indian Society of Medical and Pediatric Oncology

od 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., Reddy Kundur, Ravindra, Sekhon, Rupinder, Singhal, Manish, Smruti, B.K., SP, Somashekhar, Suryavanshi, Moushumi, Verma, Amit
Wydane w JCO Glob Oncol (2020)