1. A mutation in IFT43 causes non-syndromic recessive retinal degeneration. (18th September 2017) Authors: Biswas, Pooja; Duncan, Jacque L; Ali, Muhammad; Matsui, Hiroko; Naeem, Muhammad Asif; Raghavendra, Pongali B; Frazer, Kelly A; Arts, Heleen H; Riazuddin, Sheikh; Akram, Javed; Hejtmancik, J Fielding; Riazuddin, S Amer; Ayyagari, Radha Journal: Human molecular genetics Issue: Volume 26:Number 23(2017:Dec. 01) Page Start: 4741 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Adaptive call admission control scheme with optimal resource allocation for multi-class cellular networks. (2015) Authors: Sharma, Abhijit; Kar, Purna; Biswas, Pooja; Bhattacharya, Uma Journal: International journal of autonomous and adaptive communications systems Issue: Volume 8:Number 4(2015) Page Start: 353 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Cover, Volume 42, Issue 2. Issue 2 (25th January 2021) Authors: Biswas, Pooja; Borooah, Shyamanga; Matsui, Hiroko; Voronchikhina, Marina; Zhou, Jason; Zawaydeh, Qais; Raghavendra, Pongali B.; Ferreyra, Henry; Riazuddin, S. Amer; Wahlin, Karl; Frazer, Kelly A.; Ayyagari, Radha Journal: Human mutation Issue: Volume 42:Issue 2(2021) Page Start: i Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Cover, Volume 42, Issue 2. Issue 2 (25th January 2021) Authors: Biswas, Pooja; Borooah, Shyamanga; Matsui, Hiroko; Voronchikhina, Marina; Zhou, Jason; Zawaydeh, Qais; Raghavendra, Pongali B.; Ferreyra, Henry; Riazuddin, S. Amer; Wahlin, Karl; Frazer, Kelly A.; Ayyagari, Radha Journal: Human mutation Issue: Volume 42:Issue 2(2021) Page Start: i Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Detection and validation of novel mutations in MERTK in a simplex case of retinal degeneration using WGS and hiPSC–RPEs model. Issue 2 (13th December 2020) Authors: Biswas, Pooja; Borooah, Shyamanga; Matsui, Hiroko; Voronchikhina, Marina; Zhou, Jason; Zawaydeh, Qais; Raghavendra, Pongali B.; Ferreyra, Henry; Riazuddin, S. Amer; Wahlin, Karl; Frazer, Kelly A.; Ayyagari, Radha Journal: Human mutation Issue: Volume 42:Issue 2(2021) Page Start: 189 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Identification of the genetic determinants responsible for retinal degeneration in families of Mexican descent. (2nd January 2018) Authors: Villanueva, Adda; Biswas, Pooja; Kishaba, Kameron; Suk, John; Tadimeti, Keerti; Raghavendra, Pongali B; Nadeau, Karine; Lamontagne, Bruno; Busque, Lambert; Geoffroy, Steve; Mongrain, Ian; Asselin, Géraldine; Provost, Sylvie; Dubé, Marie-Pierre; Nudleman, Eric; Ayyagari, Radha Journal: Ophthalmic genetics Issue: Volume 39:Number 1(2018) Page Start: 73 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Late‐onset retinal degeneration pathology due to mutations in CTRP5 is mediated through HTRA1. Issue 6 (5th August 2019) Authors: Chekuri, Anil; Zientara‐Rytter, Katarzyna; Soto‐Hermida, Angel; Borooah, Shyamanga; Voronchikhina, Marina; Biswas, Pooja; Kumar, Virender; Goodsell, David; Hayward, Caroline; Shaw, Peter; Stanton, Chloe; Garland, Donita; Subramani, Suresh; Ayyagari, Radha Journal: Aging cell Issue: Volume 18:Issue 6(2019) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Ocular Phenotype of a Family with FAM161A-associated Retinal Degeneration. (2nd January 2016) Authors: Duncan, Jacque L.; Biswas, Pooja; Kozak, Igor; Navani, Mili; Syed, Reema; Soudry, Shiri; Menghini, Moreno; Caruso, Rafael C.; Jeffrey, Brett G.; Heckenlively, John R.; Reddy, G. Bhanuprakash; Lee, Pauline; Roorda, Austin; Ayyagari, Radha Journal: Ophthalmic genetics Issue: Volume 37:Number 1(2016) Page Start: 44 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Whole genome sequencing reveals novel mutations causing autosomal dominant inherited macular degeneration. (2nd November 2018) Authors: Borooah, Shyamanga; Stanton, Chloe M.; Marsh, Joseph; Carss, Keren J.; Waseem, Naushin; Biswas, Pooja; Agorogiannis, Georgios; Raymond, Lucy; Arno, Gavin; Webster, Andrew R. Journal: Ophthalmic genetics Issue: Volume 39:Number 6(2018) Page Start: 763 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗