"Until every African patient with a Rare Disease is diagnosed!" Research group at Stellenbosch University, directed by Prof Shahida Moosa @shahida_moosa

Joined October 2020
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#RareDiseaseMonth2025 [15/02/2025] Join us for an evening of music, dance & art to support #RareDisease "Rare Talent for Rare Disease" concert featuring @cjbcompany, capechoral.com, SU wind band, Gerhard Joubert, Jason Marshall & others! Tickets: shorturl.at/MRKhM
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Welcome Lilian! We are so excited to have you here, wishing you a fun time in Cape Town, learning genomics and variant interpretation! Solve some genomes for our #RareDisease patients!
A huge welcome to #GHA_SciEX exchange student, Lilian Arnold, who ✈️ from @uni_tue 🇩🇪to @StellenboschUni 🇿🇦 ➡️ @shahida_moosa lab for a 2 months stay. Thrilled to learn with and from you! 👏 Kudos to the GHA-SciEx powered by @CoRE_GHA & @unibern #Training #Opportunity
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First diagnosis made today by Lili!!! 😍🥳
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RareDiseaseGenomicsRSA retweeted
🏆 We’re proud to celebrate Prof @shahida_moosa prestigious win at the 2025 @NSTF_SA  Awards Her leadership in @RareGenomicsRSA is advancing world-class research & shaping the next generation of scientists 👏 Congrats, Prof Moosa! #MBHG is proud to be home to such excellence
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RareDiseaseGenomicsRSA retweeted
17 Jun 2025
Congratulations to Prof Shahida Moosa, on her extraordinary achievement as a finalist for the NSTF-SAMRC Clinician-Scientist Award of the prestigious NSTF-South32 Awards – the Science Oscars of South Africa (SA). The Awards recognise outstanding contributions to #science, #engineering, #technology (SET) and #innovation in SA since 1998. She is the Head of Medical Genetics at Tygerberg Hospital and Professor of Medical Genetics at @StellenboschUni; and also in the TW-Kamule-NSTF Emerging Researcher category. * Genomics for Health in Africa is a first of its kind in sub-Saharan Africa, and is revolutionising clinical genomics and precision medicine on the continent. The project aims to provide diagnoses to the 100 million Africans living with undiagnosed rare diseases and familial cancers. The programme’s motto is “Until every African with a Rare Disease and Cancer is diagnosed”. Using the latest in genomic technology, coupled with outstanding clinical and bioinformatic expertise and novel AI-tools, GHA has thus far been able to diagnose more than half of the participants enrolled, many of whom are the first in Africa with their diagnoses. GHA aims to leave no-one behind, extends its impact from bedside to laboratory and back again, and provides increased access to needed genomic testing to underserved and underrepresented African populations from South Africa to Rwanda and beyond. See the list of all finalists who are contending as finalists for the best contributions to SET and innovation in SA under 16 different categories: nstf.org.za/current-finalist… @South32 @SAMRC #NSTFawards2025 #scienceoscars #research #scientificresearch #development #KnowledgeBasedEconomy #sciencerolemodels #scienceexcellence #socioeconomicgrowth
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RareDiseaseGenomicsRSA retweeted
20 Jun 2025
Congratulations to Prof Shahida Moosa, on her extraordinary achievement as a finalist for the TW Kambule-NSTF Award: Emerging Researcher of the prestigious NSTF-South32 Awards – the Science Oscars of South Africa (SA). The Awards recognise outstanding contributions to #science, #engineering, #technology (SET) and #innovation in SA since 1998. She is the Head: Medical Genetics, Tygerberg Hospital; Professor: Medical Genetics at the @StellenboschUni and also, in the NSTF-SAMRC Clinician-Scientist category*. Genomics for Health in Africa is a first of its kind in sub-Saharan Africa and is revolutionising clinical genomics and precision medicine on the continent. The project aims to provide diagnoses to the 100 million Africans living with undiagnosed rare diseases and familial cancers. The programme’s motto is “Until every African with a Rare Disease and Cancer is diagnosed”. Using the latest in genomic technology, coupled with outstanding clinical and bioinformatic expertise and novel AI-tools, GHA has thus far been able to diagnose more than half of the participants enrolled, many of whom are the first in Africa with their diagnoses. GHA aims to leave no-one behind, extends its impact from bedside to laboratory and back again, and provides increased access to needed genomic testing to underserved and underrepresented African populations from South Africa to Rwanda and beyond. See the list of all finalists who are contending as finalists for the best contributions to SET and innovation in SA under 16 different categories: nstf.org.za/current-finalist…@South32 #NSTFawards2025 #scienceoscars #research #scientificresearch #development #KnowledgeBasedEconomy #sciencerolemodels #scienceexcellence #socioeconomicgrowth
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#NewBuggy Thanks to very generous donors, Little L got his 1st buggy today: now he can zoom around in this amazing stroller, which can fold & is easy to transport on the taxi! Shout out to the amazing @SydneyStel @SyngapNetwork @cureSYNGAP1 - for making this happen! #CureSyngap
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That's us: Co-Lead for Genomics in Health in Africa. Dream made reality by our Prof @shahida_moosa #ResearchForImpact in Africa, for Africans, by Africans "Until every African with a #RareDisease and #Cancer is diagnosed!" @CoRE_GHA @SUhealthsci @SuMBHG
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RareDiseaseGenomicsRSA retweeted
14 Mar 2025
📣New today! 📄De novo variants in CDKL1 and CDKL2 are associated with neurodevelopmental symptoms 🧑‍🤝‍🧑@KancaOguz & @UDNconnect colleagues cell.com/ajhg/abstract/S0002…

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RareDiseaseGenomicsRSA retweeted
I think the @RareGenomicsRSA team and Prof @shahida_moosa doesn't get the level of credit they deserve. We spend millions of Rands telling the stories of other countries, but little to no credit for our own. @geordinhl please let our citizens know about these about these Heroes
#RareDiseaseMonth Wednesdays in Feb are sandwich days: we package and deliver delicious sandwiches and fruit to the patients at the Paediatric outpatients at Tygerberg Hospital, including those attending #Genetic Clinic. 1 smile at a time... @shahida_moosa @SUhealthsci @SuMBHG
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RareDiseaseGenomicsRSA retweeted
A reminder that abstract submissions for the ISCB Africa ASBCB Bioinformatics conference in Cape Town in April close on February 20th. Travel fellowships will be available for African students with accepted talks, info will be on the website soon: iscb.org/africa2025/home

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#RareDiseaseMonth Fridays in Feb are cupcake days! Spreading awareness about #RareDiseases - 1 cupcake at a time! Thanks for all the support @SUhealthsci @SuMBHG @shahida_moosa
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#RareDiseaseMonth Wednesdays in Feb are sandwich days: we package and deliver delicious sandwiches and fruit to the patients at the Paediatric outpatients at Tygerberg Hospital, including those attending #Genetic Clinic. 1 smile at a time... @shahida_moosa @SUhealthsci @SuMBHG
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There are still tickets available to attend this amazing event - It is going to be spectacular, just look at the line up of artists who will be performing! Buy a ticket or 3 or 4! See you there this Saturday! @MatiesResearch @StellenboschUni @SUglobally @PostdocSU @StelliesSRC
#RareDiseaseMonth2025 [15/02/2025] Join us for an evening of music, dance & art to support #RareDisease "Rare Talent for Rare Disease" concert featuring @cjbcompany, capechoral.com, SU wind band, Gerhard Joubert, Jason Marshall & others! Tickets: shorturl.at/MRKhM
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RareDiseaseGenomicsRSA retweeted
Prof @shahida_moosa is presenting on “Genetics of facial morphology recognition”. We need more images and more diversity to make AI more efficient she purports. GMDB is an app everyone can be involved in for the benefit of others. #AfSHG2025 #Africa #Genetics
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RareDiseaseGenomicsRSA retweeted
Interesting panel discussion from the session 1 speakers on AI, Machine Learning and Data Science. Topics presented and dissected ranged from “Application of AI in Cancer Genomics”, Alzheimer’s Disease and Retinopathy. #AfSHG2025 #Africa #Genomics #WomenInSTEM
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RareDiseaseGenomicsRSA retweeted
#AfSHG in Uganda- early birds taking part in a workshop on clinical databases and resources used in #RareDisease and #Cancer clinics and research. Participants and faculty from across the continent, speaking several languages! @aimelumaka @AfSHG_Genetics @RareGenomicsRSA
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RareDiseaseGenomicsRSA retweeted
Support rare disease patients by joining the Rare Disease Charity Art Auction! 🎨 Bid on stunning A1 canvas prints by Cumine van Tonder, blending nature & anatomy. 💖 Every bid brings hope. Visit bidpro.co.za/AuctionDetails/… & follow @raredgsa. 💜 #MakeADifference
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RareDiseaseGenomicsRSA retweeted
It’s a privilege to announce Solve-RD’s latest manuscript based on years of work: “Genomic reanalysis of a pan-European rare-disease resource yields new diagnoses” nature.com/articles/s41591-0… A thread (1/n)
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Very proud of Malwandla! And welcome to Stellenbosch University! #RareDiseases #OI #BrittleBones @OsteogenesisImperfecta People with Rare Diseases Shining Brightly! 😍 @BrittleBoneUK @brittlebonessa
Malwandla Baloyi, SA’s top matric achiever for learners with disabilities, has her sights set on studying Psychology at Stellenbosch. Despite living with brittle bone disease, her resilience inspires us all. We’re rooting for you, Malwandla! tinyurl.com/mw72s9vw #FutureMatie
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