| Investigating the molecular basis of retinal degeneration in a familial cohort of Pakistani decent by exome sequencing B Maranhao, P Biswas, ADH Gottsch, M Navani, MA Naeem, J Suk, J Chu, ... PLoS One 10 (9), e0136561, 2015 | 40 | 2015 |
| Establishing the involvement of the novel gene AGBL5 in retinitis pigmentosa by whole genome sequencing K Branham, H Matsui, P Biswas, AA Guru, M Hicks, JJ Suk, H Li, ... Physiological Genomics 48 (12), 922-927, 2016 | 34 | 2016 |
| Genetic analysis of 10 pedigrees with inherited retinal degeneration by exome sequencing and phenotype-genotype association P Biswas, JL Duncan, B Maranhao, I Kozak, K Branham, L Gabriel, JH Lin, ... Physiological genomics 49 (4), 216-229, 2017 | 28 | 2017 |
| exomeSuite: Whole exome sequence variant filtering tool for rapid identification of putative disease causing SNVs/indels B Maranhao, P Biswas, JL Duncan, KE Branham, GA Silva, MA Naeem, ... Genomics 103 (2-3), 169-176, 2014 | 28 | 2014 |
| Late‐onset retinal degeneration pathology due to mutations in CTRP5 is mediated through HTRA1 A Chekuri, K Zientara‐Rytter, A Soto‐Hermida, S Borooah, ... Aging Cell 18 (6), e13011, 2019 | 26 | 2019 |
| IFT88 mutations identified in individuals with non-syndromic recessive retinal degeneration result in abnormal ciliogenesis A Chekuri, AA Guru, P Biswas, K Branham, S Borooah, A Soto-Hermida, ... Human genetics 137, 447-458, 2018 | 22 | 2018 |
| A missense mutation in ASRGL1 is involved in causing autosomal recessive retinal degeneration P Biswas, VRM Chavali, G Agnello, E Stone, C Chakarova, JL Duncan, ... Human molecular genetics 25 (12), 2483-2497, 2016 | 21 | 2016 |
| Ocular phenotype of a family with FAM161A-associated retinal degeneration JL Duncan, P Biswas, I Kozak, M Navani, R Syed, S Soudry, M Menghini, ... Ophthalmic genetics 37 (1), 44-52, 2016 | 19 | 2016 |
| Whole genome sequencing revealed mutations in two independent genes as the underlying cause of retinal degeneration in an Ashkenazi Jewish pedigree K Gustafson, JL Duncan, P Biswas, A Soto-Hermida, H Matsui, ... Genes 8 (9), 210, 2017 | 15 | 2017 |
| Transcriptome analysis of orbital adipose tissue in active thyroid eye disease using next generation RNA sequencing technology BW Lee, VB Kumar, P Biswas, AC Ko, RM Alameddine, DB Granet, ... The open ophthalmology journal 12, 41, 2018 | 14 | 2018 |
| Deciphering the genetic architecture and ethnographic distribution of IRD in three ethnic populations by whole genome sequence analysis P Biswas, AL Villanueva, A Soto-Hermida, JL Duncan, H Matsui, ... PLoS genetics 17 (10), e1009848, 2021 | 13 | 2021 |
| Whole genome sequencing reveals novel mutations causing autosomal dominant inherited macular degeneration S Borooah, CM Stanton, J Marsh, KJ Carss, N Waseem, P Biswas, ... Ophthalmic genetics 39 (6), 763-770, 2018 | 13 | 2018 |
| Identification of the genetic determinants responsible for retinal degeneration in families of Mexican descent A Villanueva, P Biswas, K Kishaba, J Suk, K Tadimeti, PB Raghavendra, ... Ophthalmic genetics 39 (1), 73-79, 2018 | 13 | 2018 |
| A mutation in IFT43 causes non-syndromic recessive retinal degeneration P Biswas, JL Duncan, M Ali, H Matsui, MA Naeem, PB Raghavendra, ... Human molecular genetics 26 (23), 4741-4751, 2017 | 13 | 2017 |
| Whole-exome sequencing identifies novel variants that co-segregates with autosomal recessive retinal degeneration in a Pakistani pedigree P Biswas, MA Naeem, MH Ali, MZ Assir, SN Khan, S Riazuddin, ... Retinal Degenerative Diseases: Mechanisms and Experimental Therapy, 219-228, 2018 | 5 | 2018 |
| Detection and validation of novel mutations in MERTK in a simplex case of retinal degeneration using WGS and hiPSC–RPEs model P Biswas, S Borooah, H Matsui, M Voronchikhina, J Zhou, Q Zawaydeh, ... Human mutation 42 (2), 189-199, 2021 | 4 | 2021 |
| Identification of novel deletions as the underlying cause of retinal degeneration in two pedigrees K Branham, AA Guru, I Kozak, P Biswas, M Othman, K Kishaba, ... Retinal Degenerative Diseases: Mechanisms and Experimental Therapy, 229-236, 2018 | 4 | 2018 |
| Avidity sequencing of whole genomes from retinal degeneration pedigrees identifies causal variants P Biswas, A Villanueva, BJ Krajacich, J Moreno, J Zhao, AM Berry, ... medRxiv, 2022.12. 27.22283803, 2022 | 3 | 2022 |
| Identification of causative mutations in consanguineous pedigrees from Pakistan with recessive retinal degeneration by whole exome analysis P Biswas, B Maranhao, P Lee, J Suk, M Navani, S Khan, N Butt, ... Investigative Ophthalmology & Visual Science 54 (15), 3349-3349, 2013 | 2 | 2013 |
| A Diasporic Mythography: Myth, Legend and Memory in the Literature of the Indian Diaspora PM Biswas Academia Lunare, Luna Press Publishing, 2021 | 1 | 2021 |
