Ehsan Ullah, Ph.D. (@ehsanullahx) header
Ehsan Ullah, Ph.D. (@ehsanullahx) profile picture

Medical Geneticist | LGG | AAUR- QAU - UCSF | RTs are not endorsements! Opinions are my own! 🇵🇰🇺🇸

Maryland, USA
Joined August 2022
Photo by Ehsan Ullah, Ph.D. (@ehsanullahx)Photo by Ehsan Ullah, Ph.D. (@ehsanullahx)Photo by Ehsan Ullah, Ph.D. (@ehsanullahx)Photo by Ehsan Ullah, Ph.D. (@ehsanullahx)Photo by Ehsan Ullah, Ph.D. (@ehsanullahx)Photo by Ehsan Ullah, Ph.D. (@ehsanullahx)Photo by Ehsan Ullah, Ph.D. (@ehsanullahx)Photo by Ehsan Ullah, Ph.D. (@ehsanullahx)Photo by Ehsan Ullah, Ph.D. (@ehsanullahx)Photo by Ehsan Ullah, Ph.D. (@ehsanullahx)
I graduated from the Clinical Laboratory Genetics and Genomics Fellowship Program at @genome_gov ! Thank you everyone who were a part of this incredible journey ! Congratulations to my graduating friends, you all are really smart! @GenomicsMatters @HufnagelLab @TACGeneMD
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Dear friends! I am requesting prayers for my elder brother @Inam_Ullah1980 , who will be shortly going through cardiac bypass surgery! May Allah SWT bless him with speedy healing and complete recovery! Ameen Summa Ameen @hamzashafqaat @SardarZimri
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Thrilled to share our new @NatureComms paper! We identified NR6A1 variants causing a novel oculo-vertebral-renal syndrome, bringing answers to a family after 20 years. Read more: rdcu.be/euFcZ #RareDisease #Genomics @NatEyeInstitute #GeneChat @NIH
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Ehsan Ullah, Ph.D. retweeted
The new Disney Pixar movie Elio has the main character sporting an eye patch. This seems like a good time to spread the word about amblyopia, the treatment for it, and #NIHfunded research on brain-based causes of vision loss. brnw.ch/21wU0DC
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Congratulations to Steven J Fliesler, PhD, for receiving the 2025 Stockton Kimball Award in recognition of outstanding scientific achievement and service. #NIHfunded #retina @Jacobs_Med_UB Details: brnw.ch/21wTrp8
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RT @FranMartinezGr: Homozygous variants in EIF3K associated with neurodevelopmental delay, microcephaly, and growth retardation #RareDisease #Genetics #morbidgene cell.com/hgg-advances/fullte…
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Awesome work from some of my dear colleagues and friends!
RT @FranMartinezGr: Biallelic null variants in C19orf44 cause a unique late onset retinal dystrophy phenotype characterized by patchy perifoveal chorioretinal atrophy #RareDisease #Genetics #morbidgene sciencedirect.com/science/ar…
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Ehsan Ullah, Ph.D. retweeted
Excited to announce Dr. Farran Briggs will join @NatEyeInstitute as Senior Investigator in the Laboratory of Sensorimotor Research. Most recently at @UofR, Briggs brings an impressive record of #optogenetics & functional ultrasound research, charismatic training & mentoring.
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Ehsan Ullah, Ph.D. retweeted
Is there synergistic heterozygosity in double heterozygotes of pathogenic variants in SLC3A1 and SLC7A9? bit.ly/3YC5LHm #Cystinuria #PopulationGenetics
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Ehsan Ullah, Ph.D. retweeted
Sniffles2 @lfpaulin detects mosaic SVs with Alu insertions compared to short read sequencing. Time for long read sequencing to better identify these difficult variants! #ASHG24 – at Denver, CO
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Ehsan Ullah, Ph.D. retweeted
Luis Paulin on detection of mosaics structural variation with Sniffles2 #ASHG24
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I will present a poster on molecular diagnosis of optic atrophy! Follow the attached image for details! It is great to be back at #ashg24 this year in Denver CO.
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Fantastic work and the plenary talk. #ashg24
Giovanni Quinones-Valdez on long read RNA seq to study alternative splicing #ASHG24
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Ehsan Ullah, Ph.D. retweeted
Giovanni Quinones-Valdez on long read RNA seq to study alternative splicing #ASHG24
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