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Edward Yang

TitleAsst Prof-Clinical Dept
InstitutionUniversity of Chicago
DepartmentRadiology
AddressChicago IL 60637
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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. Abu-El-Haija A, Bayat A, Mancilar H, Uctepe E, Esen FN, Tumer S, Metli K, Yesilyurt A, Jamra RA, Lalani S, Levy R, Mihalek I, Redler S, Mullegama SV, Umair M, Wegler M, Nawaz S, Yang E, Bodamer O. Biallelic Novel SKOR2 Variants in Individuals With Cerebellar Hypoplasia and Intellectual Disability, Expanding the Phenotypic Spectrum of Valence-Farazi Cerebellar Ataxia Syndrome. Am J Med Genet A. 2026 Jul; 200(7):1725-1739. PMID: 41821366.
      Citations:    Fields:    Translation:Humans
    2. Mealer RG, Anderson JJ, Smith SL, Masters BM, Barth SH, Huizar KDJ, Sran S, Yoon H, Ringland A, Muron SJ, Bowyer ME, D'Gama AM, Poduri A, Lidov HGW, Yang E, Furnari J, Canoll PD, Ostendorf AP, Koboldt DC, Pierson CR, Thomas DL, Philpot BD, Noel M, Cummings RD, Heinzen EL, Bedrosian TA. Disrupted O-GalNAc glycosylation as a mechanism and biomarker of SLC35A2-associated epilepsy. bioRxiv. 2026 Mar 04. PMID: 41867720; PMCID: PMC13001337.
      Citations:    
    3. Berry GT, Vos EN, Demirbas D, Brucker W, Gilmartin A, Lehtinen MK, Yang E, Prabhu SP, Chen J, Huang X, Qi W, Bennett MJ, Haynes RL, Rodan L, Poduri A, Pearl PL, Rotenberg A, He M, Rubio-Gozalbo ME. A patient with a rare metabolic disease and myo-inositol administration leading to a new treatment for epilepsy. Mol Genet Metab. 2026 Jun; 148(2):109871. PMID: 41875761; PMCID: PMC13568792.
      Citations:    Fields:    
    4. Lai A, Neil JE, Akula SK, Amrom D, Andermann E, Bergin A, Caraballo R, Chen AY, Gaitanis J, Mochida GH, Gotoff JM, Kuchukhidze G, Marom D, ElAchkar CM, Regev M, Rodan LH, Olson H, Zhang B, Poduri A, Shao DD, Walsh CA, Yang E. Diverse Genetic Etiologies of Unilateral Polymicrogyria. Ann Neurol. 2026 May; 99(5):1277-1286. PMID: 41670011; PMCID: PMC13033188.
      Citations:    Fields:    Translation:Humans
    5. Khoshkhoo S, Bae M, Wang Y, Tillett A, Ramirez RB, Finander B, Egan ED, Marx L, Patel D, Zhou Z, Chahine Y, Chhouk B, Zoullas SM, Lai A, Coras R, Bielle F, Navarro V, Mathon B, Valiante TA, Moradi Chameh H, Gao AF, Krings T, Gooley S, Hildebrand MS, Bulluss K, Clark J, Morokoff AP, King JA, Todaro M, Kwan P, O'Brien TJ, Berkovic SF, Scheffer IE, Perucca P, Lapinskas E, Rolston JD, Cosgrove GR, Sarkis RA, D'Gama AM, Alexadrescu S, Yang E, Poduri A, Richardson RM, Erson-Omay EZ, DeLanerolle N, Spencer DD, Brown KS, Miller MB, Roberts AE, Santos LN, Kontaridis MI, Bien CG, Blacklow SC, Kahle KT, Blümcke I, Huang AY, Lee EA, Walsh CA. Activating Ras-MAPK pathway variants drive hippocampal clonal competition in human epilepsy. bioRxiv. 2026 Jan 27. PMID: 41659639; PMCID: PMC12873922.
      Citations:    
    6. Naomi Vos E, Demirbas D, Rodan L, Yang E, Prabhu SP, Chen J, Huang X, Haynes RL, Lehtinen MK, Bennett MJ, He M, Pearl PL, Rubio-Gozalbo ME, Poduri A, Berry GT, Vos EN, Demirbas D, Rodan L, Yang E, Prabhu SP, Chen J, Huang X, Qi W, Haynes RL, Lehtinen MK, Bennett MJ, He M, Pearl PL, Rubio-Gozalbo ME, Poduri A, Berry GT. The Use of Synaptic Extracellular Myo-Inositol to Treat Developmental and Epileptic Encephalopathy. Ann Child Neurol Soc. 2025 Sep; 3(3):201-207. PMID: 40880844; PMCID: PMC12381637.
      Citations: 1     
    7. Bizzotto S, Talukdar M, Stronge EA, Ramirez RB, Yang Y, Huang AY, Hu Q, Hou Y, Hylton NK, Finander B, Tillett A, Zhou Z, Chhouk BH, D'Gama AM, Yang E, Green TE, Reutens DC, Mullen SA, Scheffer IE, Hildebrand MS, Buono RJ, Blümcke I, Poduri AH, Khoshkhoo S, Walsh CA. Cell-type-informed genotyping of mosaic focal epilepsies reveals cell-autonomous and non-cell-autonomous disease-associated transcriptional programs. Proc Natl Acad Sci U S A. 2025 Jul 22; 122(29):e2509622122. PMID: 40674414; PMCID: PMC12305027.
      Citations: 6     Fields:    Translation:HumansCells
    8. Ngouchet Nouhossi JL, Minga I, Szasz T, Truong VT, Johnson AE, Yang E, Kotlo S, Subashchandran V, Medina F, Zareba KM, Goyal A, Simonetti OP, Patel AR, Singulane CC, Singh J, Nadig V, Fadl S, Trankle CR, Sarswat N, Patel HN, Mor-Avi V, Smith B, Slivnick JA. Disparities in diagnosis and outcomes in American patients with transthyretin cardiac amyloidosis. Int J Cardiovasc Imaging. 2025 Aug; 41(8):1487-1496. PMID: 40474003; PMCID: PMC12397186.
      Citations: 2     Fields:    Translation:Humans
    9. Beck A, Gabler-Pamer L, Alencastro Veiga Cruzeiro G, Lambo S, Englinger B, Shaw ML, Hack OA, Liu I, Haase RD, de Biagi CAO, Baumgartner A, Nascimento Silva AD, Klenner M, Freidel PS, Herms J, von Baumgarten L, Tonn JC, Thon N, Bruckner K, Madlener S, Mayr L, Senfter D, Peyrl A, Slavc I, Lötsch D, Dorfer C, Geyregger R, Amberg N, Haberler C, Mack N, Schwalm B, Pfister SM, Korshunov A, Baird LC, Yang E, Chi SN, Alexandrescu S, Gojo J, Kool M, Hovestadt V, Filbin MG. Cellular hierarchies of embryonal tumors with multilayered rosettes are shaped by oncogenic microRNAs and receptor-ligand interactions. Nat Cancer. 2025 Jun; 6(6):1035-1055. PMID: 40419763; PMCID: PMC12202505.
      Citations: 4     Fields:    Translation:HumansCells
    10. van Gool R, Cay M, Ren B, Brodeur K, Golden E, Goodlett B, Yang E, Reilly T, Hastings C, Berry-Kravis EM, Lee PY, Di Biase M, Cropley V, Pantelis C, Velakoulis D, Shinn AK, Al-Hertani W, Walterfang M, Upadhyay J. Implications of the choroid plexus in Niemann-Pick disease Type C neuropathogenesis. Brain Behav Immun. 2025 Feb; 124:376-384. PMID: 39689839; PMCID: PMC11787871.
      Citations:    Fields:    Translation:Humans
    11. German CA, Yang E. Coronary Artery Calcium Scoring in the Assessment of ASCVD Risk. J Cardiopulm Rehabil Prev. 2024 05 01; 44(3):E7-E8. PMID: 38465913.
      Citations:    Fields:    Translation:Humans
    12. Miller KE, Rivaldi AC, Shinagawa N, Sran S, Navarro JB, Westfall JJ, Miller AR, Roberts RD, Akkari Y, Supinger R, Hester ME, Marhabaie M, Gade M, Lu J, Rodziyevska O, Bhattacharjee MB, Von Allmen GK, Yang E, Lidov HGW, Harini C, Shah MN, Leonard J, Pindrik J, Shaikhouni A, Goldman JE, Pierson CR, Thomas DL, Boué DR, Ostendorf AP, Mardis ER, Poduri A, Koboldt DC, Heinzen EL, Bedrosian TA. Post-zygotic rescue of meiotic errors causes brain mosaicism and focal epilepsy. Nat Genet. 2023 11; 55(11):1920-1928. PMID: 37872450; PMCID: PMC10714261.
      Citations: 15     Fields:    Translation:Humans
    13. Akula SK, Chen AY, Neil JE, Shao DD, Mo A, Hylton NK, DiTroia S, Ganesh VS, Smith RS, O'Kane K, Yeh RC, Marciano JH, Kirkham S, Kenny CJ, Song JHT, Al Saffar M, Millan F, Harris DJ, Murphy AV, Klemp KC, Braddock SR, Brand H, Wong I, Talkowski ME, O'Donnell-Luria A, Lai A, Hill RS, Mochida GH, Doan RN, Barkovich AJ, Yang E, Amrom D, Andermann E, Poduri A, Walsh CA, Polymicrogyria Genetics Research Network. Exome Sequencing and the Identification of New Genes and Shared Mechanisms in Polymicrogyria. JAMA Neurol. 2023 09 01; 80(9):980-988. PMID: 37486637; PMCID: PMC10366952.
      Citations: 14     Fields:    Translation:Humans
    14. Yang E, Balkhy HH, Patel B, Cotella J, Landeras L, Addetia K, Slivnick JA. Cardiovascular computed tomography for the detection of quadricuspid aortic valve: A case report. Radiol Case Rep. 2023 Oct; 18(10):3544-3548. PMID: 37547798; PMCID: PMC10403715.
      Citations:    
    15. Sakpichaisakul K, El-Dib M, Munster C, Supapannachart KJ, Yang E, Walsh BH, Volpe JJ, Inder TE. Amplitude-Integrated Electroencephalography Evolution and Magnetic Resonance Imaging Injury in Mild and Moderate to Severe Neonatal Encephalopathy. Am J Perinatol. 2024 05; 41(S 01):e2463-e2473. PMID: 37369240.
      Citations:    Fields:    Translation:Humans
    16. Khoshkhoo S, Wang Y, Chahine Y, Erson-Omay EZ, Robert SM, Kiziltug E, Damisah EC, Nelson-Williams C, Zhu G, Kong W, Huang AY, Stronge E, Phillips HW, Chhouk BH, Bizzotto S, Chen MH, Adikari TN, Ye Z, Witkowski T, Lai D, Lee N, Lokan J, Scheffer IE, Berkovic SF, Haider S, Hildebrand MS, Yang E, Gunel M, Lifton RP, Richardson RM, Blümcke I, Alexandrescu S, Huttner A, Heinzen EL, Zhu J, Poduri A, DeLanerolle N, Spencer DD, Lee EA, Walsh CA, Kahle KT. Contribution of Somatic Ras/Raf/Mitogen-Activated Protein Kinase Variants in the Hippocampus in Drug-Resistant Mesial Temporal Lobe Epilepsy. JAMA Neurol. 2023 Jun 01; 80(6):578-587. PMID: 37126322; PMCID: PMC10152377.
      Citations: 33     Fields:    Translation:Humans
    17. Saffari A, Kellner M, Jordan C, Rosengarten H, Mo A, Zhang B, Strelko O, Neuser S, Davis MY, Yoshikura N, Futamura N, Takeuchi T, Nabatame S, Ishiura H, Tsuji S, Aldeen HS, Cali E, Rocca C, Houlden H, Efthymiou S, Assmann B, Yoon G, Trombetta BA, Kivisäkk P, Eichler F, Nan H, Takiyama Y, Tessa A, Santorelli FM, Sahin M, Blackstone C, Yang E, Schüle R, Ebrahimi-Fakhari D. The clinical and molecular spectrum of ZFYVE26-associated hereditary spastic paraplegia: SPG15. Brain. 2023 05 02; 146(5):2003-2015. PMID: 36315648; PMCID: PMC10411936.
      Citations: 10     Fields:    Translation:Humans
    18. Qian X, DeGennaro EM, Talukdar M, Akula SK, Lai A, Shao DD, Gonzalez D, Marciano JH, Smith RS, Hylton NK, Yang E, Bazan JF, Barrett L, Yeh RC, Hill RS, Beck SG, Otani A, Angad J, Mitani T, Posey JE, Pehlivan D, Calame D, Aydin H, Yesilbas O, Parks KC, Argilli E, England E, Im K, Taranath A, Scott HS, Barnett CP, Arts P, Sherr EH, Lupski JR, Walsh CA. Loss of non-motor kinesin KIF26A causes congenital brain malformations via dysregulated neuronal migration and axonal growth as well as apoptosis. Dev Cell. 2022 10 24; 57(20):2381-2396.e13. PMID: 36228617; PMCID: PMC10585591.
      Citations: 10     Fields:    Translation:HumansAnimalsCells
    19. Lai A, Soucy A, El Achkar CM, Barkovich AJ, Cao Y, DiStefano M, Evenson M, Guerrini R, Knight D, Lee YS, Mefford HC, Miller DT, Mirzaa G, Mochida G, Rodan LH, Patel M, Smith L, Spencer S, Walsh CA, Yang E, Yuskaitis CJ, Yu T, Poduri A, ClinGen Brain Malformation Variant Curation Expert Panel. The ClinGen Brain Malformation Variant Curation Expert Panel: Rules for somatic variants in AKT3, MTOR, PIK3CA, and PIK3R2. Genet Med. 2022 11; 24(11):2240-2248. PMID: 35997716; PMCID: PMC9883838.
      Citations: 9     Fields:    Translation:Humans
    20. Andzelm MM, Balasubramaniam S, Yang E, Compton AG, Millington K, Zhu J, Anselm I, Rodan LH, Thorburn DR, Christodoulou J, Srivastava S. Expansion of the clinical and neuroimaging spectrum associated with NDUFS8-related disorder. JIMD Rep. 2022 Sep; 63(5):391-399. PMID: 36101822; PMCID: PMC9458602.
      Citations: 1     
    21. Nijman M, Yang E, Jaimes C, Prohl AK, Sahin M, Krueger DA, Wu JY, Northrup H, Stone SSD, Madsen JR, Fallah A, Blount JP, Weiner HL, Grayson L, Bebin EM, Porter BE, Warfield SK, Prabhu SP, Peters JM, TACERN Study Group. Limited utility of structural MRI to identify the epileptogenic zone in young children with tuberous sclerosis. J Neuroimaging. 2022 09; 32(5):991-1000. PMID: 35729081; PMCID: PMC11267633.
      Citations: 2     Fields:    Translation:Humans
    22. van Gool R, Tucker-Bartley A, Yang E, Todd N, Guenther F, Goodlett B, Al-Hertani W, Bodamer OA, Upadhyay J. Targeting neurological abnormalities in lysosomal storage diseases. Trends Pharmacol Sci. 2022 06; 43(6):495-509. PMID: 34844772.
      Citations: 8     Fields:    Translation:HumansCells
    23. Sakpichaisakul K, Supapannachart KJ, El-DIb M, Szakmar E, Yang E, Walsh BH, Robinson JN, Cherkerzian S, Volpe JJ, Inder TE. Blood gas measures as predictors for neonatal encephalopathy severity. J Perinatol. 2021 09; 41(9):2261-2269. PMID: 34168288.
      Citations: 2     Fields:    Translation:Humans
    24. Shao DD, Straussberg R, Ahmed H, Khan A, Tian S, Hill RS, Smith RS, Majmundar AJ, Ameziane N, Neil JE, Yang E, Al Tenaiji A, Jamuar SS, Schlaeger TM, Al-Saffar M, Hovel I, Al-Shamsi A, Basel-Salmon L, Amir AZ, Rento LM, Lim JY, Ganesan I, Shril S, Evrony G, Barkovich AJ, Bauer P, Hildebrandt F, Dong M, Borck G, Beetz C, Al-Gazali L, Eyaid W, Walsh CA. A recurrent, homozygous EMC10 frameshift variant is associated with a syndrome of developmental delay with variable seizures and dysmorphic features. Genet Med. 2021 06; 23(6):1158-1162. PMID: 33531666; PMCID: PMC8187145.
      Citations: 14     Fields:    Translation:Humans
    25. Jaimes C, Robson CD, Machado-Rivas F, Yang E, Mahan K, Bixby SD, Robertson RL. Success of Nonsedated Neuroradiologic MRI in Children 1-7 Years Old. AJR Am J Roentgenol. 2021 05; 216(5):1370-1377. PMID: 32783551.
      Citations: 26     Fields:    Translation:Humans
    26. Kodani A, Kenny C, Lai A, Gonzalez DM, Stronge E, Sejourne GM, Isacco L, Partlow JN, O'Donnell A, McWalter K, Byrne AB, Barkovich AJ, Yang E, Hill RS, Gawlinski P, Wiszniewski W, Cohen JS, Fatemi SA, Baranano KW, Sahin M, Vossler DG, Yuskaitis CJ, Walsh CA. Posterior Neocortex-Specific Regulation of Neuronal Migration by CEP85L Identifies Maternal Centriole-Dependent Activation of CDK5. Neuron. 2020 04 22; 106(2):246-255.e6. PMID: 32097629; PMCID: PMC7255387.
      Citations: 10     Fields:    Translation:HumansCells
    27. Lyon GJ, Marchi E, Ekstein J, Meiner V, Hirsch Y, Scher S, Yang E, De Vivo DC, Madrid R, Li Q, Wang K, Haworth A, Chilton I, Chung WK, Velinov M. VAC14 syndrome in two siblings with retinitis pigmentosa and neurodegeneration with brain iron accumulation. Cold Spring Harb Mol Case Stud. 2019 12; 5(6). PMID: 31387860; PMCID: PMC6913149.
      Citations: 7     Fields:    Translation:Humans
    28. Dias CM, Punetha J, Zheng C, Mazaheri N, Rad A, Efthymiou S, Petersen A, Dehghani M, Pehlivan D, Partlow JN, Posey JE, Salpietro V, Gezdirici A, Malamiri RA, Al Menabawy NM, Selim LA, Vahidi Mehrjardi MY, Banu S, Polla DL, Yang E, Rezazadeh Varaghchi J, Mitani T, van Beusekom E, Najafi M, Sedaghat A, Keller-Ramey J, Durham L, Coban-Akdemir Z, Karaca E, Orlova V, Schaeken LLM, Sherafat A, Jhangiani SN, Stanley V, Shariati G, Galehdari H, Gleeson JG, Walsh CA, Lupski JR, Seiradake E, Houlden H, van Bokhoven H, Maroofian R. Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder. Am J Hum Genet. 2019 11 07; 105(5):1048-1056. PMID: 31668703; PMCID: PMC6849109.
      Citations: 25     Fields:    Translation:Humans
    29. Kelly M, Park M, Mihalek I, Rochtus A, Gramm M, Pérez-Palma E, Axeen ET, Hung CY, Olson H, Swanson L, Anselm I, Briere LC, High FA, Sweetser DA, Undiagnosed Diseases Network, Kayani S, Snyder M, Calvert S, Scheffer IE, Yang E, Waugh JL, Lal D, Bodamer O, Poduri A. Spectrum of neurodevelopmental disease associated with the GNAO1 guanosine triphosphate-binding region. Epilepsia. 2019 03; 60(3):406-418. PMID: 30682224; PMCID: PMC6452443.
      Citations: 40     Fields:    Translation:Humans
    30. Yun HJ, Chung AW, Vasung L, Yang E, Tarui T, Rollins CK, Ortinau CM, Grant PE, Im K. Automatic labeling of cortical sulci for the human fetal brain based on spatio-temporal information of gyrification. Neuroimage. 2019 03; 188:473-482. PMID: 30553042; PMCID: PMC6452886.
      Citations: 14     Fields:    Translation:Humans
    31. Coulter ME, Dorobantu CM, Lodewijk GA, Delalande F, Cianferani S, Ganesh VS, Smith RS, Lim ET, Xu CS, Pang S, Wong ET, Lidov HGW, Calicchio ML, Yang E, Gonzalez DM, Schlaeger TM, Mochida GH, Hess H, Lee WA, Lehtinen MK, Kirchhausen T, Haussler D, Jacobs FMJ, Gaudin R, Walsh CA. The ESCRT-III Protein CHMP1A Mediates Secretion of Sonic Hedgehog on a Distinctive Subtype of Extracellular Vesicles. Cell Rep. 2018 07 24; 24(4):973-986.e8. PMID: 30044992; PMCID: PMC6178983.
      Citations: 65     Fields:    Translation:HumansAnimalsCells
    32. Torres A, Brownstein CA, Tembulkar SK, Graber K, Genetti C, Kleiman RJ, Sweadner KJ, Mavros C, Liu KX, Smedemark-Margulies N, Maski K, Yang E, Agrawal PB, Shi J, Beggs AH, D'Angelo E, Lincoln SH, Carroll D, Dedeoglu F, Gahl WA, Biggs CM, Swoboda KJ, Berry GT, Gonzalez-Heydrich J. De novo ATP1A3 and compound heterozygous NLRP3 mutations in a child with autism spectrum disorder, episodic fatigue and somnolence, and muckle-wells syndrome. Mol Genet Metab Rep. 2018 Sep; 16:23-29. PMID: 29922587; PMCID: PMC6005789.
      Citations: 9     
    33. Olson HE, Jean-Marçais N, Yang E, Heron D, Tatton-Brown K, van der Zwaag PA, Bijlsma EK, Krock BL, Backer E, Kamsteeg EJ, Sinnema M, Reijnders MRF, Bearden D, Begtrup A, Telegrafi A, Lunsing RJ, Burglen L, Lesca G, Cho MT, Smith LA, Sheidley BR, Moufawad El Achkar C, Pearl PL, Poduri A, Skraban CM, Tarpinian J, Nesbitt AI, Fransen van de Putte DE, Ruivenkamp CAL, Rump P, Chatron N, Sabatier I, De Bellescize J, Guibaud L, Sweetser DA, Waxler JL, Wierenga KJ, DDD Study, Donadieu J, Narayanan V, Ramsey KM, C4RCD Research Group, Nava C, Rivière JB, Vitobello A, Tran Mau-Them F, Philippe C, Bruel AL, Duffourd Y, Thomas L, Lelieveld SH, Schuurs-Hoeijmakers J, Brunner HG, Keren B, Thevenon J, Faivre L, Thomas G, Thauvin-Robinet C. A Recurrent De Novo PACS2 Heterozygous Missense Variant Causes Neonatal-Onset Developmental Epileptic Encephalopathy, Facial Dysmorphism, and Cerebellar Dysgenesis. Am J Hum Genet. 2018 05 03; 102(5):995-1007. PMID: 29656858; PMCID: PMC5986694.
      Citations: 29     Fields:    Translation:Humans
    34. D'Gama AM, Woodworth MB, Hossain AA, Bizzotto S, Hatem NE, LaCoursiere CM, Najm I, Ying Z, Yang E, Barkovich AJ, Kwiatkowski DJ, Vinters HV, Madsen JR, Mathern GW, Blümcke I, Poduri A, Walsh CA. Somatic Mutations Activating the mTOR Pathway in Dorsal Telencephalic Progenitors Cause a Continuum of Cortical Dysplasias. Cell Rep. 2017 12 26; 21(13):3754-3766. PMID: 29281825; PMCID: PMC5752134.
      Citations: 175     Fields:    Translation:HumansAnimalsCells
    35. Walsh BH, Neil J, Morey J, Yang E, Silvera MV, Inder TE, Ortinau C. The Frequency and Severity of Magnetic Resonance Imaging Abnormalities in Infants with Mild Neonatal Encephalopathy. J Pediatr. 2017 08; 187:26-33.e1. PMID: 28479101; PMCID: PMC5533615.
      Citations: 33     Fields:    Translation:Humans
    36. Peyton C, Yang E, Kocherginsky M, Adde L, Bos AF, Schreiber MD, Msall ME, Fjørtoft T, Støen R, Einspieler C. Relationship between white matter pathology and performance on the General Movement Assessment and the Test of Infant Motor Performance in very preterm infants. Early Hum Dev. 2016 Apr; 95:23-7. PMID: 26925933.
      Citations: 9     Fields:    Translation:Humans
    37. O'Rawe JA, Wu Y, Dörfel MJ, Rope AF, Au PY, Parboosingh JS, Moon S, Kousi M, Kosma K, Smith CS, Tzetis M, Schuette JL, Hufnagel RB, Prada CE, Martinez F, Orellana C, Crain J, Caro-Llopis A, Oltra S, Monfort S, Jiménez-Barrón LT, Swensen J, Ellingwood S, Smith R, Fang H, Ospina S, Stegmann S, Den Hollander N, Mittelman D, Highnam G, Robison R, Yang E, Faivre L, Roubertie A, Rivière JB, Monaghan KG, Wang K, Davis EE, Katsanis N, Kalscheuer VM, Wang EH, Metcalfe K, Kleefstra T, Innes AM, Kitsiou-Tzeli S, Rosello M, Keegan CE, Lyon GJ. TAF1 Variants Are Associated with Dysmorphic Features, Intellectual Disability, and Neurological Manifestations. Am J Hum Genet. 2015 Dec 03; 97(6):922-32. PMID: 26637982; PMCID: PMC4678794.
      Citations: 65     Fields:    Translation:HumansAnimalsCells
    38. Hansford BG, Albert D, Yang E. Classic neuroimaging findings of nonketotic hyperglycemia on computed tomography and magnetic resonance imaging with absence of typical movement disorder symptoms (hemichorea-hemiballism). J Radiol Case Rep. 2013 Aug; 7(8):1-9. PMID: 24421947; PMCID: PMC3888174.
      Citations: 19     Fields:    Translation:Humans
    39. Wu EX, Wu Y, Tang H, Wang J, Yang J, Ng MC, Yang ES, Chan CW, Zhu S, Lau CP, Tse HF. Study of myocardial fiber pathway using magnetic resonance diffusion tensor imaging. Magn Reson Imaging. 2007 Sep; 25(7):1048-57. PMID: 17707167.
      Citations: 16     Fields:    Translation:AnimalsCells
    40. Li G, Ng MC, Wong KK, Luk KD, Yang ES. Spinal effects of acupuncture stimulation assessed by proton density-weighted functional magnetic resonance imaging at 0.2 T. Magn Reson Imaging. 2005 Dec; 23(10):995-9. PMID: 16376183.
      Citations: 4     Fields:    Translation:Humans
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