InstitutionBaylor College of Medicine
DepartmentDepartment of Molecular & Human Genetics
Houston, TX 77030
vCardDownload vCard

    Collapse Bibliographic 
    Collapse selected publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
    Newest   |   Oldest   |   Most Cited   |   Most Discussed   |   Timeline   |   Field Summary   |   Plain Text
    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Hayeck TJ, Stong N, Baugh E, Dhindsa R, Turner TN, Malakar A, Mosbruger TL, Shaw GT, Duan Y, Ionita-Laza I, Goldstein D, Allen AS. Ancestry adjustment improves genome-wide estimates of regional intolerance. Genetics. 2022 05 31; 221(2). PMID: 35385101.
      Citations:    Fields:    Translation:Humans
    2. Vasavda C, Semenza ER, Liew J, Kothari R, Dhindsa RS, Shanmukha S, Lin A, Tokhunts R, Ricco C, Snowman AM, Albacarys L, Pastore F, Ripoli C, Grassi C, Barone E, Kornberg MD, Dong X, Paul BD, Snyder SH. Biliverdin reductase bridges focal adhesion kinase to Src to modulate synaptic signaling. Sci Signal. 2022 05 10; 15(733):eabh3066. PMID: 35536885.
      Citations:    Fields:    Translation:AnimalsCells
    3. Koko M, Motelow JE, Stanley KE, Bobbili DR, Dhindsa RS, May P. Association of ultra-rare coding variants with genetic generalized epilepsy: A case-control whole exome sequencing study. Epilepsia. 2022 03; 63(3):723-735. PMID: 35032048.
      Citations:    Fields:    Translation:Humans
    4. Zoghbi AW, Dhindsa RS, Goldberg TE, Mehralizade A, Motelow JE, Wang X, Alkelai A, Harms MB, Lieberman JA, Markx S, Goldstein DB. High-impact rare genetic variants in severe schizophrenia. Proc Natl Acad Sci U S A. 2021 12 21; 118(51). PMID: 34903660.
      Citations:    Fields:    Translation:Humans
    5. Wang Q, Dhindsa RS, Carss K, Harper AR, Nag A, Tachmazidou I, Vitsios D, Deevi SVV, Mackay A, Muthas D, Hühn M, Monkley S, Olsson H, Wasilewski S, Smith KR, March R, Platt A, Haefliger C, Petrovski S. Rare variant contribution to human disease in 281,104 UK Biobank exomes. Nature. 2021 09; 597(7877):527-532. PMID: 34375979.
      Citations: 16     Fields:    Translation:Humans
    6. Dhindsa RS, Mattsson J, Nag A, Wang Q, Wain LV, Allen R, Wigmore EM, Ibanez K, Vitsios D, Deevi SVV, Wasilewski S, Karlsson M, Lassi G, Olsson H, Muthas D, Monkley S, Mackay A, Murray L, Young S, Haefliger C, Maher TM, Belvisi MG, Jenkins G, Molyneaux PL, Platt A, Petrovski S. Identification of a missense variant in SPDL1 associated with idiopathic pulmonary fibrosis. Commun Biol. 2021 03 23; 4(1):392. PMID: 33758299.
      Citations: 2     Translation:Humans
    7. Vitsios D, Dhindsa RS, Middleton L, Gussow AB, Petrovski S. Prioritizing non-coding regions based on human genomic constraint and sequence context with deep learning. Nat Commun. 2021 03 08; 12(1):1504. PMID: 33686085.
      Citations: 3     Fields:    Translation:Humans
    8. Dhindsa RS, Zoghbi AW, Krizay DK, Vasavda C, Goldstein DB. A Transcriptome-Based Drug Discovery Paradigm for Neurodevelopmental Disorders. Ann Neurol. 2021 02; 89(2):199-211. PMID: 33159466.
      Citations: 3     Fields:    Translation:HumansAnimalsCells
    9. Dhindsa RS, Copeland BR, Mustoe AM, Goldstein DB. Natural Selection Shapes Codon Usage in the Human Genome. Am J Hum Genet. 2020 07 02; 107(1):83-95. PMID: 32516569.
      Citations: 14     Fields:    Translation:HumansCells
    10. Gelfman S, Wang Q, Lu YF, Hall D, Bostick CD, Dhindsa R, Halvorsen M, McSweeney KM, Cotterill E, Edinburgh T, Beaumont MA, Frankel WN, Petrovski S, Allen AS, Boland MJ, Goldstein DB, Eglen SJ. meaRtools: An R package for the analysis of neuronal networks recorded on microelectrode arrays. PLoS Comput Biol. 2018 10; 14(10):e1006506. PMID: 30273353.
      Citations: 6     Fields:    Translation:AnimalsCells
    11. Gussow AB, Copeland BR, Dhindsa RS, Wang Q, Petrovski S, Majoros WH, Allen AS, Goldstein DB. Correction: Orion: Detecting regions of the human non-coding genome that are intolerant to variation using population genetics. PLoS One. 2018; 13(1):e0191298. PMID: 29324863.
      Citations:    Fields:    
    12. Gussow AB, Copeland BR, Dhindsa RS, Wang Q, Petrovski S, Majoros WH, Allen AS, Goldstein DB. Orion: Detecting regions of the human non-coding genome that are intolerant to variation using population genetics. PLoS One. 2017; 12(8):e0181604. PMID: 28797091.
      Citations: 8     Fields:    Translation:Humans
    13. Dhindsa RS, Goldstein DB. Schizophrenia: From genetics to physiology at last. Nature. 2016 Feb 11; 530(7589):162-3. PMID: 26814972.
      Citations: 13     Fields:    Translation:HumansAnimals
    14. Dhindsa RS, Goldstein DB. Genetic Discoveries Drive Molecular Analyses and Targeted Therapeutic Options in the Epilepsies. Curr Neurol Neurosci Rep. 2015 Oct; 15(10):70. PMID: 26319171.
      Citations: 5     Fields:    Translation:HumansAnimals
    15. Petrovski S, Shashi V, Petrou S, Schoch K, McSweeney KM, Dhindsa RS, Krueger B, Crimian R, Case LE, Khalid R, El-Dairi MA, Jiang YH, Mikati MA, Goldstein DB. Exome sequencing results in successful riboflavin treatment of a rapidly progressive neurological condition. Cold Spring Harb Mol Case Stud. 2015 Oct; 1(1):a000257. PMID: 27148561.
      Citations: 8     Fields:    
    16. Dhindsa RS, Bradrick SS, Yao X, Heinzen EL, Petrovski S, Krueger BJ, Johnson MR, Frankel WN, Petrou S, Boumil RM, Goldstein DB. Epileptic encephalopathy-causing mutations in DNM1 impair synaptic vesicle endocytosis. Neurol Genet. 2015 Jun; 1(1):e4. PMID: 27066543.
      Citations: 24     
    17. Zhu X, Petrovski S, Xie P, Ruzzo EK, Lu YF, McSweeney KM, Ben-Zeev B, Nissenkorn A, Anikster Y, Oz-Levi D, Dhindsa RS, Hitomi Y, Schoch K, Spillmann RC, Heimer G, Marek-Yagel D, Tzadok M, Han Y, Worley G, Goldstein J, Jiang YH, Lancet D, Pras E, Shashi V, McHale D, Need AC, Goldstein DB. Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios. Genet Med. 2015 Oct; 17(10):774-81. PMID: 25590979.
      Citations: 146     Fields:    Translation:Humans
    DHINDSA's Networks
    Click the
    buttons for more information and interactive visualizations!
    Concepts (93)
    Co-Authors (2)
    Similar People (60)
    Same Department Expand Description