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Record W4414614684 · doi:10.1186/s13073-025-01529-2

Adult genomic medicine: lessons from a multisite study of 2700 patients

2025· article· en· W4414614684 on OpenAlexafffund
Khadijah Bakur, Halima Hamid, Bader Alhaddad, Majid Alfadhel, Amal Alhashem, Wafaa Eyaid, Talal Alanzi, Fuad Al Mutairi, Abdulrahman Alswaid, Farouq Ababneh, Malak Al Ghamdi, Sarar Mohamed, Ahmed Alaskar, Farjah Alqahtani, Hamad Alzaidan, Mohammed Al‐Owain, Eissa Faqeih, Aziza Mushiba, Basamat Almoallem, Norah Alsaleh, Saeed Al Tala, Muneera Alshammari, Alyazeed Turkistani, Ghadah Gosadi, Fahad Hakami, Fahad Alobaid, Hadeel Al Rukban, Ahmed Mohammed Alfaidi, Rola Ba‐Abbad, Mohammed A. Almuqbil, Ahmad A Al-Boukai, Ali Alshehri, Raashda A. Sulaiman, Ali Almontasheri, Enam Danish, Afaf Alsagheir, Deema Aljeaid, Bashayer S. Alawam, Aiman Shawli, Maha Alotaibi, Wed Majdali, Zohor Azher, Mohammed Almannai, Wail Ba-Alawi, Abdulaziz Baazeem, Abdulrahman Alsultan, Abdulrahman AlTahan, Abdulrahman Hummadi, Ahmed AlBadawi, Ali Alasmari, Amaal AlDakheel, Ali Awaji, Bader Alghamdi, Basma Zahid, Dalal Bubshait, Dia A. Mohammed, Elham Bagrayn, Firdous Abdulwahab, Hussein Algahtani, Iram Alluhaydan, Jameela A. Kari, Mohammed A AlHajji, Mai Labani, Moayed Aljack, Mohamed Alzawahmah, Mohammed Mahnashi, Mohammed Ali Tohary, Mohd Elsunni, Mona A. Fouda, Nizar Algarni, Nouriya Al‐Sannaa, Ohoud Alzahrani, Omar Yousef, Omnia Ahmed Abdulaty, Saeed Bohlega, Saud Abu-Harbesh, Wael Alqarawi, Yousef Housawi, Zainab AlArfaj, Lama AlAbdi, Touati Benoukraf, Fowzan S. Alkuraya

Bibliographic record

VenueGenome Medicine · 2025
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicGenomics and Rare Diseases
Canadian institutionsMemorial University of Newfoundland
FundersKing Saud bin Abdulaziz University for Health ScienceKing Khalid UniversityKing Salman Center for Disability ResearchUniversity of JeddahUmm Al-Qura UniversityImam Abdulrahman Bin Faisal UniversityMinistry of National Guard Health AffairsMemorial University of NewfoundlandKing Khaled Eye Specialist HospitalFaculty of Medicine, Memorial University of NewfoundlandKing Abdulaziz UniversityKing Saud UniversityKing Faisal Specialist Hospital and Research Centre
KeywordsHuman geneticsGenomicsPrecision medicineGenomic medicineGenome BiologySystems biologyMEDLINEPersonalized medicine

Abstract

fetched live from OpenAlex

BACKGROUND: Clinical exome and genome sequencing has transformed the diagnostic workup of patients with genetic disorders. The extensive body of evidence supporting the application of this clinical genomics approach in pediatric patients stands in stark contrast to the relative paucity of evidence for its use in the adult population. Here, we describe the largest cohort to date of adult patients who underwent clinical exome and genome sequencing for suspected genetic diagnoses. METHODS: A total of 2763 adult patients (2529 families) from all regions of Saudi Arabia are included in this cohort (2202 exomes, and 561 genomes). RESULTS: The diagnostic rate is 38.9% spanning 535 Mendelian genes and revealing clinical diagnostic errors in 38% of patients with positive reports. Structured feedback using C-GUIDE demonstrates clinical utility in 90% of positive cases. Consistent with the highly consanguineous nature of the local population, the majority (61%) of diagnosed phenotypes are recessive (94.6% homozygous) and founder variants account for 85% (414/487) of these variants. The same population characteristic has also led to the encounter of extremely rare, even novel recessive disorders including a highly penetrant novel RNF43-related hemochromatosis, NFXL1-related syndrome of hyperlaxity, short stature, and kidney disease, as well as autosomal recessive forms of typically dominant disorders. Multilocus phenotypes are observed in 5% of cases although only 26.7% of these are caused by two recessive variants. That 70% of molecular diagnoses encountered in our cohort are typically described in pediatric patients allowed us to observe highly unusual clinical presentations in the adult population. This delayed diagnosis also represents a missed opportunity for effective treatment in many instances and we note the availability of treatment for 26% of diagnosed conditions. Of particular interest are patients with monogenic disorders that could be overlooked as common multifactorial adult diseases (e.g., diabetes, dyslipidemia, stroke, chronic kidney disease, and dementia). Finally, we note the opportunities of deploying adult clinical genomics in an underrepresented population where 45.5% (373/819) of encountered variants are completely absent in gnomAD. CONCLUSIONS: Our results illustrate numerous benefits of a clinical genomics approach in adult medicine and argue for a broader implementation than currently practiced.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.628
Threshold uncertainty score0.650

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.007
GPT teacher head0.274
Teacher spread0.267 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations5
Published2025
Admission routes2
Has abstractyes

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