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HIBA SAADE

TitleInstructor
InstitutionBaylor College of Medicine
DepartmentDepartment of Pediatrics
Address6701 FANNIN
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    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.
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    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. De-Paula RB, Kim J, Rhinn H, Saade H, Chavez F, Segura T, Lozano MV, Etoundi M, Silos K, Kass N, Korchina V, Doddapaneni H, Venner E, Masdeu JC, Pavlik V, Yu MM, Lin CR, Jankovic J, Buchman AS, Muzny D, Gibbs RA, Elsea SH, Abeliovich A, Lansbury P, Vanegas-Arroyave N, Shaw CA, Shulman JM. Mapping the causal chain from genetic risk variants to lipid dysmetabolism in Parkinson's disease. Brain. 2026 Feb 02. PMID: 41627849.
      Citations: 1     Fields:    
    2. Spargo TP, Sands CF, Juan IR, Mitchell J, Ravanmehr V, Butts JC, De-Paula RB, Kim Y, Hu F, Wang Q, Vitsios D, Garg M, Middleton L, Tyrlik M, Messa M, Del Angel G, Calame DG, Saade H, Robak L, Hollis B, Cuddapah VA, Zoghbi HY, Shulman JM, Petrovski S, Al-Ramahi I, Tachmazidou I, Dhindsa RS. Haploinsufficiency of ITSN1 is associated with a substantial increased risk of Parkinson's disease. Cell Rep. 2025 Mar 25; 44(3):115355. PMID: 40056900; PMCID: PMC12124131.
      Citations: 5     Fields:    Translation:HumansAnimals
    3. Hill EJ, Robak LA, Al-Ouran R, Deger J, Fong JC, Vandeventer PJ, Schulman E, Rao S, Saade H, Savitt JM, von Coelln R, Desai N, Doddapaneni H, Salvi S, Dugan-Perez S, Muzny DM, McGuire AL, Liu Z, Gibbs RA, Shaw C, Jankovic J, Shulman LM, Shulman JM. Genome Sequencing in the Parkinson Disease Clinic. Neurol Genet. 2022 Aug; 8(4):e200002. PMID: 35747619; PMCID: PMC9210549.
      Citations:    
    4. Hill EJ, Mangleburg CG, Alfradique-Dunham I, Ripperger B, Stillwell A, Saade H, Rao S, Fagbongbe O, von Coelln R, Tarakad A, Hunter C, Dawe RJ, Jankovic J, Shulman LM, Buchman AS, Shulman JM. Quantitative mobility measures complement the MDS-UPDRS for characterization of Parkinson's disease heterogeneity. Parkinsonism Relat Disord. 2021 03; 84:105-111. PMID: 33607526; PMCID: PMC7987213.
      Citations: 2     Fields:    Translation:Humans
    5. Ahdab R, Kikano R, Saade H, Riachi N. Early corticospinal tract Wallerian degeneration versus mesencephalic substantia nigra degeneration secondary to striatal stroke. Clin Neurol Neurosurg. 2014 Mar; 118:101-2. PMID: 24468328.
      Citations:    
    6. Ahdab R, Saade HS, Kikano R, Ferzli J, Tarcha W, Riachi N. Pure ipsilateral central facial palsy and contralateral hemiparesis secondary to ventro-medial medullary stroke. J Neurol Sci. 2013 Sep 15; 332(1-2):154-5. PMID: 23849262.
      Citations:    
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