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Cell Stem Cell
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May 7, 2016
Identification and Correction of Mechanisms Underlying Inherited Blindness in Human iPSC-Derived Optic Cups
David A Parfitt, Amelia Lane, Conor M Ramsden, et al.
Plos One
|
February 19, 2021
Left ventricular myocardial strain and tissue characterization by cardiac magnetic resonance imaging in immune checkpoint inhibitor associated cardiotoxicity
Angela Y Higgins, Amit Arbune, Aaron Soufer, et al.
JAMA Ophthalmology
|
May 26, 2017
Detailed Clinical Phenotype and Molecular Genetic Findings in CLN3-Associated Isolated Retinal Degeneration
Cristy A Ku, Sarah Hull, Gavin Arno, et al.
JAMA Ophthalmology
|
March 3, 2017
Association of Steroid 5α-Reductase Type 3 Congenital Disorder of Glycosylation With Early-Onset Retinal Dystrophy
Rachel L Taylor, Gavin Arno, James A Poulter, et al.
Journal of Medical Genetics
|
November 9, 2013
Combined exome and whole-genome sequencing identifies mutations in ARMC4 as a cause of primary ciliary dyskinesia with defects in the outer dynein arm
Alexandros Onoufriadis, Amelia Shoemark, Mustafa M Munye, et al.
American Journal of Medical Genetics. Part A
|
June 14, 2019
Delineating the expanding phenotype associated with SCAPER gene mutation
James Fasham, Gavin Arno, Siying Lin, et al.
Journal of Medical Genetics
|
April 27, 2017
Missense mutations in the WD40 domain of <i>AHI1</i> cause non-syndromic retinitis pigmentosa
Thanh-Minh T Nguyen, Sarah Hull, Ronald Roepman, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance
|
May 14, 2026
Prospective Serial Cardiovascular Magnetic Resonance Imaging of Immune Checkpoint Inhibitor Myocarditis Correlates with Cardiovascular Outcomes
Jennifer M Kwan, Mohamad Khattab, Maciej Tysarowski, et al.
American Journal of Human Genetics
|
November 28, 2016
Mutations in REEP6 Cause Autosomal-Recessive Retinitis Pigmentosa
Gavin Arno, Smriti A Agrawal, Aiden Eblimit, et al.
Journal of Medical Genetics
|
December 7, 2014
Neuropathy target esterase impairments cause Oliver-McFarlane and Laurence-Moon syndromes
Robert B Hufnagel, Gavin Arno, Nichole D Hein, et al.
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of 7
Search research articles
Search
Showing results (51-60 of 66) with videos related to
Sort By:
Page
of 7
Cell Stem Cell
|
May 7, 2016
Identification and Correction of Mechanisms Underlying Inherited Blindness in Human iPSC-Derived Optic Cups
David A Parfitt, Amelia Lane, Conor M Ramsden, et al.
Plos One
|
February 19, 2021
Left ventricular myocardial strain and tissue characterization by cardiac magnetic resonance imaging in immune checkpoint inhibitor associated cardiotoxicity
Angela Y Higgins, Amit Arbune, Aaron Soufer, et al.
JAMA Ophthalmology
|
May 26, 2017
Detailed Clinical Phenotype and Molecular Genetic Findings in CLN3-Associated Isolated Retinal Degeneration
Cristy A Ku, Sarah Hull, Gavin Arno, et al.
JAMA Ophthalmology
|
March 3, 2017
Association of Steroid 5α-Reductase Type 3 Congenital Disorder of Glycosylation With Early-Onset Retinal Dystrophy
Rachel L Taylor, Gavin Arno, James A Poulter, et al.
Journal of Medical Genetics
|
November 9, 2013
Combined exome and whole-genome sequencing identifies mutations in ARMC4 as a cause of primary ciliary dyskinesia with defects in the outer dynein arm
Alexandros Onoufriadis, Amelia Shoemark, Mustafa M Munye, et al.
American Journal of Medical Genetics. Part A
|
June 14, 2019
Delineating the expanding phenotype associated with SCAPER gene mutation
James Fasham, Gavin Arno, Siying Lin, et al.
Journal of Medical Genetics
|
April 27, 2017
Missense mutations in the WD40 domain of <i>AHI1</i> cause non-syndromic retinitis pigmentosa
Thanh-Minh T Nguyen, Sarah Hull, Ronald Roepman, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance
|
May 14, 2026
Prospective Serial Cardiovascular Magnetic Resonance Imaging of Immune Checkpoint Inhibitor Myocarditis Correlates with Cardiovascular Outcomes
Jennifer M Kwan, Mohamad Khattab, Maciej Tysarowski, et al.
American Journal of Human Genetics
|
November 28, 2016
Mutations in REEP6 Cause Autosomal-Recessive Retinitis Pigmentosa
Gavin Arno, Smriti A Agrawal, Aiden Eblimit, et al.
Journal of Medical Genetics
|
December 7, 2014
Neuropathy target esterase impairments cause Oliver-McFarlane and Laurence-Moon syndromes
Robert B Hufnagel, Gavin Arno, Nichole D Hein, et al.
Page
of 7