Ketan Mishra

About me
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About me

After completing my education and an exciting Master’s project, I have been
involved in projects involving human induced pluripotent stem cells in
various laboratories in Melbourne and Sydney.
To take my interest in regenerative science further—and experience the
other side of the globe—I decided to continue my doctorate studies working
on a natural regeneration model, salamanders, and investigating the mechanism
behind their extraordinary ability to regenerate.
When I am not admiring salamanders, I am usually on a hike, reading a book, or brewing a mean espresso...

PhD candidate - CMB, Karolinska Institutet (2021-Present)
Master of Biotechnology - Deakin University/Commonwealth and Scientific Research Organisation, Australia (2014-16)
Bachelor of Biomedicine - The University of Melbourne, Australia (2011-2014)

Articles

Article: HGG ADVANCES. 2023;4(4):100237
Targeted sequencing and in vitro splice assays shed light on ABCA4-associated retinopathies missing heritability
Corradi Z; Khan M; Hitti-Malin R; Mishra K; Whelan L; Cornelis SS; Hoyng CB; Kampjarvi K; Klaver CCW; Liskova P; Stoehr H; Weber BHF; Banfi S; Farrar GJ; Sharon D; Zernant J; Allikmets R; Dhaenens C-M; Cremers FPM
Article: CIRCULATION. GENOMIC AND PRECISION MEDICINE. 2022;15(4):e003527-277
Exploring the Genetic Architecture of Spontaneous Coronary Artery Dissection Using Whole-Genome Sequencing
Tarr I; Hesselson S; Iismaa SE; Rath E; Monger S; Troup M; Mishra K; Wong CMY; Hsu P-C; Junday K; Humphreys DT; Adlam D; Webb TR; Baranowska-Clarke AA; Hamby SE; Carss KJ; Samani NJ; Bax M; McGrath-Cadell L; Kovacic JC; Dunwoodie SL; Fatkin D; Muller DWM; Graham RM; Giannoulatou E
Article: INVESTIGATIVE OPHTHALMOLOGY AND VISUAL SCIENCE. 2022;63(4):20
ABCA4 c.859-25A>G, a Frequent Palestinian Founder Mutation Affecting the Intron 7 Branchpoint, Is Associated With Early-Onset Stargardt Disease
Corradi Z; Salameh M; Khan M; Heon E; Mishra K; Hitti-Malin RJ; AlSwaiti Y; Aslanian A; Banin E; Brooks BP; Zein WM; Hufnagel RB; Roosing S; Dhaenens C-M; Sharon D; Cremers FPM; AlTalbishi A
Journal article: CIRCULATION. 2021;144(Suppl_1):a11949
Abstract 11949: Disease-Specific and Comorbidity-Related Polygenic Risk in Spontaneous Coronary Artery Dissection
Tarr I; Hesselson S; Iismaa S; Troup M; Young P; Mishra K; Wong C; Junday K; Humphreys D; Dunwoodie S; Fatkin D; Muller D; Graham RM; Giannoulatou E
Article: GENETICS IN MEDICINE. 2020;22(7):1235-1246
Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics
Khan M; Cornelis SS; Del Pozo-Valero M; Whelan L; Runhart EH; Mishra K; Bults F; AlSwaiti Y; AlTalbishi A; De Baere E; Banfi S; Banin E; Bauwens M; Ben-Yosef T; Boon CJF; van den Born LI; Defoort S; Devos A; Dockery A; Dudakova L; Fakin A; Farrar GJ; Sallum JMF; Fujinami K; Gilissen C; Glavac D; Gorin MB; Greenberg J; Hayashi T; Hettinga YM; Hoischen A; Hoyng CB; Hufendiek K; Jaegle H; Kamakari S; Karali M; Kellner U; Klaver CCW; Kousal B; Lamey TM; MacDonald IM; Matynia A; McLaren TL; Mena MD; Meunier I; Miller R; Newman H; Ntozini B; Oldak M; Pieterse M; Podhajcer OL; Puech B; Ramesar R; Ruether K; Salameh M; Salles MV; Sharon D; Simonelli F; Spital G; Steehouwer M; Szaflik JP; Thompson JA; Thuillier C; Tracewska AM; van Zweeden M; Vincent AL; Zanlonghi X; Liskova P; Stoehr H; Roach JND; Ayuso C; Roberts L; Weber BHF; Dhaenens C-M; Cremers FPM
Article: STEM CELL RESEARCH. 2019;41:101584
Generation of VCCRIi001-A, a human induced pluripotent stem cell line, from a patient with spontaneous coronary artery dissection
Mishra K; Junday K; Wong CMY; Chan AY; Hesselson S; Muller DW; Iismaa SE; Mehta A; Graham RM
Journal article: EUROPEAN HEART JOURNAL. 2019;40(Supplement_1):ehz746.0486
P5540Familial clustering of spontaneous coronary artery dissection
McGrath-Cadell L; Hesselson S; Iismaa SE; Mishra K; Wong CMY; Fatkin D; Dunwoodie SL; Harvey R; Holloway CJ; Muller DWM; Giannoulatou E; Graham RM
Article: JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY. 2019;73(1):58-66
Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection
Adlam D; Olson TM; Combaret N; Kovacic JC; Iismaa SE; Al-Hussaini A; O'Byrne MM; Bouajila S; Georges A; Mishra K; Braund PS; d'Escamard V; Huang S; Margaritis M; Nelson CP; de Andrade M; Kadian-Dodov D; Welch CA; Mazurkiewicz S; Jeunemaitre X; Wong CMY; Giannoulatou E; Sweeting M; Muller D; Wood A; McGrath-Cadell L; Fatkin D; Dunwoodie SL; Harvey R; Holloway C; Empana J-P; Jouven X; Olin JW; Gulati R; Tweet MS; Hayes SN; Samani NJ; Graham RM; Motreff P; Bouatia-Naji N
Article: METHODS IN MOLECULAR BIOLOGY. 2019;1940:47-61
Production of High-Titer Lentiviral Particles for Stable Genetic Modification of Mammalian Cells.
Larcombe MR; Manent J; Chen J; Mishra K; Liu X; Nefzger CM
Journal article: HEART LUNG AND CIRCULATION. 2019;28:s330
Familial Clustering of Spontaneous Coronary Artery Dissection
McGrath-Cadell L; Hesselson S; Iismaa S; Mishra K; Wong C; Fatkin D; Dunwoodie S; Harvey R; Holloway C; Muller D; Giannoulatou E; Graham R
Article: NATURE METHODS. 2017;14(11):1055-1062
Comprehensive characterization of distinct states of human naive pluripotency generated by reprogramming
Liu X; Nefzger CM; Rossello FJ; Chen J; Knaupp AS; Firas J; Ford E; Pflueger J; Paynter JM; Chy HS; O'Brien CM; Huang C; Mishra K; Hodgson-Garms M; Jansz N; Williams SM; Blewitt ME; Nilsson SK; Schittenhelm RB; Laslett AL; Lister R; Polo JM

All other publications

Conference publication: CIRCULATION. 2021;144
Disease-Specific and Comorbidity-Related Polygenic Risk in Spontaneous Coronary Artery Dissection
Tarr I; Hesselson S; Iismaa S; Troup M; Young P; Mishra K; Wong C; Junday K; Humphreys D; Dunwoodie S; Fatkin D; Muller D; Graham RM; Giannoulatou E
Conference publication: INVESTIGATIVE OPHTHALMOLOGY AND VISUAL SCIENCE. 2021;62(8)
Identification and functional analysis of novel deep intronic and structural ABCA4 variants in 876 Stargardt disease cases
Corradi Z; Khan M; Mishra K; Whelan L; Hitti-Malin R; Cornelis S; Dhaenens C-M; Farrar GJ; Sharon D; Cremers FPM
Preprint: BIORXIV. 2019
Resolving the dark matter of ABCA4 for 1,054 Stargardt disease probands through integrated genomics and transcriptomics
Khan M; Cornelis SS; del Pozo-Valero M; Whelan L; Runhart EH; Mishra K; Bults F; AlSwaiti Y; AlTabishi A; De Baere E; Banfi S; Banin E; Bauwens M; Ben-Yosef T; Boon CJF; van den Born LI; Defoort S; Devos A; Dockery A; Dudakova L; Fakin A; Farrar GJ; Sallum JMF; Fujinami K; Gilissen C; Glavač D; Gorin MB; Greenberg J; Hayashi T; Hettinga Y; Hoischen A; Hoyng CB; Hufendiek K; Jägle H; Kamakari S; Karali M; Kellner U; Klaver CCW; Kousal B; Lamey T; MacDonald IM; Matynia A; McLaren T; Mena MD; Meunier I; Miller R; Newman H; Ntozini B; Oldak M; Pieterse M; Podhajcer OL; Puech B; Ramesar R; Rüther K; Salameh M; Salles MV; Sharon D; Simonelli F; Spital G; Steehouwer M; Szaflik JP; Thompson JA; Thuillier C; Tracewska AM; van Zweeden M; Vincent AL; Zanlonghi X; Liskova P; Stöhr H; De Roach J; Ayuso C; Roberts L; Weber BHF; Dhaenens C-M; Cremers FPM

About me

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