Konstantinos Zarbalis

Title(s)Professor in Residence, MED: Pathology & Lab Medicine
SchoolSchool of Medicine
AddressShriners Hospital
CA 95817
Phone916-453-2189
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    Collapse Research 
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    Mosaic analysis with double markers in the study of neuronal migration disorders
    NIH R21MH115347Aug 1, 2018 - Jun 30, 2021
    Role: Principal Investigator
    Craniofacial Defects in the Manta-Ray Line: A Novel Model for Ribosomopathies
    NIH R01DE022830Jan 1, 2015 - Dec 31, 2019
    Role: Principal Investigator
    Wdfy3, a novel regulator of neuronal migration and connectivity
    NIH R21HD067855Jan 1, 2011 - Jun 30, 2013
    Role: Principal Investigator

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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    Altmetrics Details 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. Prenatal folic acid and vitamin B12 imbalance alter neuronal morphology and synaptic density in the mouse neocortex. Commun Biol. 2023 11 08; 6(1):1133. Tat L, Cannizzaro N, Schaaf Z, Racherla S, Bottiglieri T, Green R, Zarbalis KS. PMID: 37938221; PMCID: PMC10632462.
      View in: PubMed   Mentions: Translation:AnimalsCells
    2. Correction: WDFY3 mutation alters laminar position and morphology of cortical neurons. Mol Autism. 2023 Jan 31; 14(1):4. Schaaf ZA, Tat L, Cannizzaro N, Panoutsopoulos AA, Green R, Rülicke T, Hippenmeyer S, Zarbalis KS. PMID: 36721238; PMCID: PMC9887812.
      View in: PubMed   Mentions:    Fields:    
    3. A genome-wide CRISPR screen identifies WDFY3 as a regulator of macrophage efferocytosis. Nat Commun. 2022 12 24; 13(1):7929. Shi J, Wu X, Wang Z, Li F, Meng Y, Moore RM, Cui J, Xue C, Croce KR, Yurdagul A, Doench JG, Li W, Zarbalis KS, Tabas I, Yamamoto A, Zhang H. PMID: 36566259; PMCID: PMC9789999.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansAnimalsCells
    4. WDFY3 mutation alters laminar position and morphology of cortical neurons. Mol Autism. 2022 06 22; 13(1):27. Schaaf ZA, Tat L, Cannizzaro N, Panoutsopoulos AA, Green R, Rülicke T, Hippenmeyer S, Zarbalis KS. PMID: 35733184; PMCID: PMC9219247.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansAnimalsCells
    5. Editorial: Autophagy in Mammalian Development and Differentiation. Front Cell Dev Biol. 2021; 9:722821. Di Bartolomeo S, Latella L, Zarbalis K, Di Sano F. PMID: 34386502; PMCID: PMC8353183.
      View in: PubMed   Mentions: 1  
    6. Wdfy3 regulates glycophagy, mitophagy, and synaptic plasticity. J Cereb Blood Flow Metab. 2021 12; 41(12):3213-3231. Napoli E, Panoutsopoulos AA, Kysar P, Satriya N, Sterling K, Shibata B, Imai D, Ruskin DN, Zarbalis KS, Giulivi C. PMID: 34187232; PMCID: PMC8669292.
      View in: PubMed   Mentions: 2     Fields:    Translation:AnimalsCells
    7. Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1. Autophagy. 2021 Jan; 17(1):1-382. Klionsky DJ, Abdel-Aziz AK, Abdelfatah S, Abdellatif M, Abdoli A, Abel S, Abeliovich H, Abildgaard MH, Abudu YP, Acevedo-Arozena A, Adamopoulos IE, Adeli K, Adolph TE, Adornetto A, Aflaki E, Agam G, Agarwal A, Aggarwal BB, Agnello M, Agostinis P, Agrewala JN, Agrotis A, Aguilar PV, Ahmad ST, Ahmed ZM, Ahumada-Castro U, Aits S, Aizawa S, Akkoc Y, Akoumianaki T, Akpinar HA, Al-Abd AM, Al-Akra L, Al-Gharaibeh A, Alaoui-Jamali MA, Alberti S, Alcocer-Gómez E, Alessandri C, Ali M, Alim Al-Bari MA, Aliwaini S, Alizadeh J, Almacellas E, Almasan A, Alonso A, Alonso GD, Altan-Bonnet N, Altieri DC, Álvarez ÉMC, Alves S, Alves da Costa C, Alzaharna MM, Amadio M, Amantini C, Amaral C, Ambrosio S, Amer AO, Ammanathan V, An Z, Andersen SU, Andrabi SA, Andrade-Silva M, Andres AM, Angelini S, Ann D, Anozie UC, Ansari MY, Antas P, Antebi A, Antón Z, Anwar T, Apetoh L, Apostolova N, Araki T, Araki Y, Arasaki K, Araújo WL, Araya J, Arden C, Arévalo MA, Arguelles S, Arias E, Arikkath J, Arimoto H, Ariosa AR, Armstrong-James D, Arnauné-Pelloquin L, Aroca A, Arroyo DS, Arsov I, Artero R, Asaro DML, Aschner M, Ashrafizadeh M, Ashur-Fabian O, Atanasov AG, Au AK, Auberger P, Auner HW, Aurelian L, Autelli R, Avagliano L, Ávalos Y, Aveic S, Aveleira CA, Avin-Wittenberg T, Aydin Y, Ayton S, Ayyadevara S, Azzopardi M, Baba M, Backer JM, Backues SK, Bae DH, Bae ON, Bae SH, Baehrecke EH, Baek A, Baek SH, Baek SH, Bagetta G, Bagniewska-Zadworna A, Bai H, Bai J, Bai X, Bai Y, Bairagi N, Baksi S, Balbi T, Baldari CT, Balduini W, Ballabio A, Ballester M, Balazadeh S, Balzan R, Bandopadhyay R, Banerjee S, Banerjee S, Bánréti Á, Bao Y, Baptista MS, Baracca A, Barbati C, Bargiela A, Barilà D, Barlow PG, Barmada SJ, Barreiro E, Barreto GE, Bartek J, Bartel B, Bartolome A, Barve GR, Basagoudanavar SH, Bassham DC, Bast RC, Basu A, Batoko H, Batten I, Baulieu EE, Baumgarner BL, Bayry J, Beale R, Beau I, Beaumatin F, Bechara LRG, Beck GR, Beers MF, Begun J, Behrends C, Behrens GMN, Bei R, Bejarano E, Bel S, Behl C, Belaid A, Belgareh-Touzé N, Bellarosa C, Belleudi F, Belló Pérez M, Bello-Morales R, Beltran JSO, Beltran S, Benbrook DM, Bendorius M, Benitez BA, Benito-Cuesta I, Bensalem J, Berchtold MW, Berezowska S, Bergamaschi D, Bergami M, Bergmann A, Berliocchi L, Berlioz-Torrent C, Bernard A, Berthoux L, Besirli CG, Besteiro S, Betin VM, Beyaert R, Bezbradica JS, Bhaskar K, Bhatia-Kissova I, Bhattacharya R, Bhattacharya S, Bhattacharyya S, Bhuiyan MS, Bhutia SK, Bi L, Bi X, Biden TJ, Bijian K, Billes VA, Binart N, Bincoletto C, Birgisdottir AB, Bjorkoy G, Blanco G, Blas-Garcia A, Blasiak J, Blomgran R, Blomgren K, Blum JS, Boada-Romero E, Boban M, Boesze-Battaglia K, Boeuf P, Boland B, Bomont P, Bonaldo P, Bonam SR, Bonfili L, Bonifacino JS, Boone BA, Bootman MD, Bordi M, Borner C, Bornhauser BC, Borthakur G, Bosch J, Bose S, Botana LM, Botas J, Boulanger CM, Boulton ME, Bourdenx M, Bourgeois B, Bourke NM, Bousquet G, Boya P, Bozhkov PV, Bozi LHM, Bozkurt TO, Brackney DE, Brandts CH, Braun RJ, Braus GH, Bravo-Sagua R, Bravo-San Pedro JM, Brest P, Bringer MA, Briones-Herrera A, Broaddus VC, Brodersen P, Brodsky JL, Brody SL, Bronson PG, Bronstein JM, Brown CN, Brown RE, Brum PC, Brumell JH, Brunetti-Pierri N, Bruno D, Bryson-Richardson RJ, Bucci C, Buchrieser C, Bueno M, Buitrago-Molina LE, Buraschi S, Buch S, Buchan JR, Buckingham EM, Budak H, Budini M, Bultynck G, Burada F, Burgoyne JR, Burón MI, Bustos V, Büttner S, Butturini E, Byrd A, Cabas I, Cabrera-Benitez S, Cadwell K, Cai J, Cai L, Cai Q, Cairó M, Calbet JA, Caldwell GA, Caldwell KA, Call JA, Calvani R, Calvo AC, Calvo-Rubio Barrera M, Camara NO, Camonis JH, Camougrand N, Campanella M, Campbell EM, Campbell-Valois FX, Campello S, Campesi I, Campos JC, et al. PMID: 33634751; PMCID: PMC7996087.
      View in: PubMed   Mentions: 1041     Fields:    Translation:HumansAnimalsCells
    8. Deficient or Excess Folic Acid Supply During Pregnancy Alter Cortical Neurodevelopment in Mouse Offspring. Cereb Cortex. 2021 01 01; 31(1):635-649. Harlan De Crescenzo A, Panoutsopoulos AA, Tat L, Schaaf Z, Racherla S, Henderson L, Leung KY, Greene NDE, Green R, Zarbalis KS. PMID: 32995858; PMCID: PMC7727343.
      View in: PubMed   Mentions: 21     Fields:    Translation:AnimalsCells
    9. Pak1ip1 Loss-of-Function Leads to Cell Cycle Arrest, Loss of Neural Crest Cells, and Craniofacial Abnormalities. Front Cell Dev Biol. 2020; 8:510063. Panoutsopoulos AA, De Crescenzo AH, Lee A, Lu AM, Ross AP, Borodinsky LN, Marcucio R, Trainor PA, Zarbalis KS. PMID: 32984348; PMCID: PMC7490522.
      View in: PubMed   Mentions: 3  
    10. Pathogenic WDFY3 variants cause neurodevelopmental disorders and opposing effects on brain size. Brain. 2019 09 01; 142(9):2617-2630. Le Duc D, Giulivi C, Hiatt SM, Napoli E, Panoutsopoulos A, Harlan De Crescenzo A, Kotzaeridou U, Syrbe S, Anagnostou E, Azage M, Bend R, Begtrup A, Brown NJ, Büttner B, Cho MT, Cooper GM, Doering JH, Dubourg C, Everman DB, Hildebrand MS, Santos FJR, Kellam B, Keller-Ramey J, Lemke JR, Liu S, Niyazov D, Payne K, Person R, Quélin C, Schnur RE, Smith BT, Strober J, Walker S, Wallis M, Walsh L, Yang S, Yuen RKC, Ziegler A, Sticht H, Pride MC, Orosco L, Martínez-Cerdeño V, Silverman JL, Crawley JN, Scherer SW, Zarbalis KS, Jamra R. PMID: 31327001; PMCID: PMC6736092.
      View in: PubMed   Mentions: 23     Fields:    Translation:HumansAnimalsCells
    11. Beyond autophagy: a novel role for autism-linked Wdfy3 in brain mitophagy. Sci Rep. 2018 07 27; 8(1):11348. Napoli E, Song G, Panoutsopoulos A, Riyadh MA, Kaushik G, Halmai J, Levenson R, Zarbalis KS, Giulivi C. PMID: 30054502; PMCID: PMC6063930.
      View in: PubMed   Mentions: 31     Fields:    Translation:AnimalsCells
    12. Lipid-based DNA/siRNA transfection agents disrupt neuronal bioenergetics and mitophagy. Biochem J. 2017 11 10; 474(23):3887-3902. Napoli E, Liu S, Marsilio I, Zarbalis K, Giulivi C. PMID: 29025974.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    13. Corrigendum to "Autophagy-linked FYVE containing protein WDFY3 interacts with TRAF6 and modulates RANKL-induced osteoclastogenesis" [J. Autoimmun. 73C (2016) 73-84]. J Autoimmun. 2017 11; 84:132. Wu DJ, Gu R, Sarin R, Zavodovskaya R, Chen CP, Christiansen BA, Zarbalis KS, Adamopoulos IE. PMID: 28757133.
      View in: PubMed   Mentions:    Fields:    
    14. Germline Chd8 haploinsufficiency alters brain development in mouse. Nat Neurosci. 2017 Aug; 20(8):1062-1073. Gompers AL, Su-Feher L, Ellegood J, Copping NA, Riyadh MA, Stradleigh TW, Pride MC, Schaffler MD, Wade AA, Catta-Preta R, Zdilar I, Louis S, Kaushik G, Mannion BJ, Plajzer-Frick I, Afzal V, Visel A, Pennacchio LA, Dickel DE, Lerch JP, Crawley JN, Zarbalis KS, Silverman JL, Nord AS. PMID: 28671691; PMCID: PMC6008102.
      View in: PubMed   Mentions: 120     Fields:    Translation:AnimalsCells
    15. Autophagy-linked FYVE containing protein WDFY3 interacts with TRAF6 and modulates RANKL-induced osteoclastogenesis. J Autoimmun. 2016 09; 73:73-84. Wu DJ, Gu R, Sarin R, Zavodovskaya R, Chen CP, Christiansen BA, Adamopoulos IE. PMID: 27330028; PMCID: PMC5003737.
      View in: PubMed   Mentions: 14     Fields:    Translation:AnimalsCells
    16. Maternal exposure to carbamazepine at environmental concentrations can cross intestinal and placental barriers. Biochem Biophys Res Commun. 2016 May 27; 474(2):291-295. Kaushik G, Huber DP, Aho K, Finney B, Bearden S, Zarbalis KS, Thomas MA. PMID: 27105911; PMCID: PMC4891464.
      View in: PubMed   Mentions: 7     Fields:    Translation:AnimalsPHPublic Health
    17. Prenatal Neurogenesis in Autism Spectrum Disorders. Front Chem. 2016; 4:12. Kaushik G, Zarbalis KS. PMID: 27014681; PMCID: PMC4791366.
      View in: PubMed   Mentions: 34  
    18. The subventricular zone continues to generate corpus callosum and rostral migratory stream astroglia in normal adult mice. J Neurosci. 2015 Mar 04; 35(9):3756-63. Sohn J, Orosco L, Guo F, Chung SH, Bannerman P, Mills Ko E, Zarbalis K, Deng W, Pleasure D. PMID: 25740506; PMCID: PMC6605576.
      View in: PubMed   Mentions: 39     Fields:    Translation:AnimalsCells
    19. Loss of Wdfy3 in mice alters cerebral cortical neurogenesis reflecting aspects of the autism pathology. Nat Commun. 2014 Sep 08; 5:4692. Orosco LA, Ross AP, Cates SL, Scott SE, Wu D, Sohn J, Pleasure D, Pleasure SJ, Adamopoulos IE, Zarbalis KS. PMID: 25198012; PMCID: PMC4159772.
      View in: PubMed   Mentions: 47     Fields:    Translation:Animals
    20. IL-17A gene transfer induces bone loss and epidermal hyperplasia associated with psoriatic arthritis. Ann Rheum Dis. 2015 Jun; 74(6):1284-92. Adamopoulos IE, Suzuki E, Chao CC, Gorman D, Adda S, Maverakis E, Zarbalis K, Geissler R, Asio A, Blumenschein WM, Mcclanahan T, De Waal Malefyt R, Gershwin ME, Bowman EP. PMID: 24567524; PMCID: PMC4229480.
      View in: PubMed   Mentions: 49     Fields:    Translation:AnimalsCells
    21. Neural crest-derived mesenchymal cells require Wnt signaling for their development and drive invagination of the telencephalic midline. PLoS One. 2014; 9(2):e86025. Choe Y, Zarbalis KS, Pleasure SJ. PMID: 24516524; PMCID: PMC3916303.
      View in: PubMed   Mentions: 10     Fields:    Translation:AnimalsCells
    22. The emerging roles of ribosome biogenesis in craniofacial development. Front Physiol. 2014; 5:26. Ross AP, Zarbalis KS. PMID: 24550838; PMCID: PMC3912750.
      View in: PubMed   Mentions: 26  
    23. A mutation in mouse Pak1ip1 causes orofacial clefting while human PAK1IP1 maps to 6p24 translocation breaking points associated with orofacial clefting. PLoS One. 2013; 8(7):e69333. Ross AP, Mansilla MA, Choe Y, Helminski S, Sturm R, Maute RL, May SR, Hozyasz KK, Wójcicki P, Mostowska A, Davidson B, Adamopoulos IE, Pleasure SJ, Murray JC, Zarbalis KS. PMID: 23935987; PMCID: PMC3723895.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansAnimalsCells
    24. PEDF is a novel oligodendrogenic morphogen acting on the adult SVZ and corpus callosum. J Neurosci. 2012 Aug 29; 32(35):12152-64. Sohn J, Selvaraj V, Wakayama K, Orosco L, Lee E, Crawford SE, Guo F, Lang J, Horiuchi M, Zarbalis K, Itoh T, Deng W, Pleasure D. PMID: 22933798; PMCID: PMC3457640.
      View in: PubMed   Mentions: 11     Fields:    Translation:AnimalsCells
    25. Meningeal defects alter the tangential migration of cortical interneurons in Foxc1hith/hith mice. Neural Dev. 2012 Jan 17; 7:2. Zarbalis K, Choe Y, Siegenthaler JA, Orosco LA, Pleasure SJ. PMID: 22248045; PMCID: PMC3287125.
      View in: PubMed   Mentions: 27     Fields:    Translation:AnimalsCells
    26. Retinoic Acid from the Meninges Regulates Cortical Neuron Generation. Cell. 2011 Aug 1; 146(3):486. Siegenthaler SJ, Ashique AA, Zarbalis ZK, Patterson PK, Hecht HJ, Kane KM, Folias FA, Choe CY, May MS, Kume KT, Napoli NJ, Peterson PA, Pleasure PS. .
      View in: Publisher Site   Mentions:
    27. A mutation in the pericentrin gene causes abnormal interneuron migration to the olfactory bulb in mice. Dev Biol. 2010 Apr 01; 340(1):41-53. Endoh-Yamagami S, Karkar KM, May SR, Cobos I, Thwin MT, Long JE, Ashique AM, Zarbalis K, Rubenstein JL, Peterson AS. PMID: 20096683.
      View in: PubMed   Mentions: 21     Fields:    Translation:AnimalsCells
    28. Extracellular Engrailed participates in the topographic guidance of retinal axons in vivo. Neuron. 2009 Nov 12; 64(3):355-366. Wizenmann A, Brunet I, Lam J, Sonnier L, Beurdeley M, Zarbalis K, Weisenhorn-Vogt D, Weinl C, Dwivedy A, Joliot A, Wurst W, Holt C, Prochiantz A. PMID: 19914184; PMCID: PMC4603356.
      View in: PubMed   Mentions: 59     Fields:    Translation:AnimalsCells
    29. Retinoic acid from the meninges regulates cortical neuron generation. Cell. 2009 Oct 30; 139(3):597-609. Siegenthaler JA, Ashique AM, Zarbalis K, Patterson KP, Hecht JH, Kane MA, Folias AE, Choe Y, May SR, Kume T, Napoli JL, Peterson AS, Pleasure SJ. PMID: 19879845; PMCID: PMC2772834.
      View in: PubMed   Mentions: 223     Fields:    Translation:AnimalsCells
    30. Cortical dysplasia and skull defects in mice with a Foxc1 allele reveal the role of meningeal differentiation in regulating cortical development. Proc Natl Acad Sci U S A. 2007 Aug 28; 104(35):14002-7. Zarbalis K, Siegenthaler JA, Choe Y, May SR, Peterson AS, Pleasure SJ. PMID: 17715063; PMCID: PMC1955817.
      View in: PubMed   Mentions: 57     Fields:    Translation:AnimalsCells
    31. EphA-Ephrin-A-mediated beta cell communication regulates insulin secretion from pancreatic islets. Cell. 2007 Apr 20; 129(2):359-70. Konstantinova I, Nikolova G, Ohara-Imaizumi M, Meda P, Kucera T, Zarbalis K, Wurst W, Nagamatsu S, Lammert E. PMID: 17448994.
      View in: PubMed   Mentions: 156     Fields:    Translation:HumansAnimalsCells
    32. Loss of the retrograde motor for IFT disrupts localization of Smo to cilia and prevents the expression of both activator and repressor functions of Gli. Dev Biol. 2005 Nov 15; 287(2):378-89. May SR, Ashique AM, Karlen M, Wang B, Shen Y, Zarbalis K, Reiter J, Ericson J, Peterson AS. PMID: 16229832.
      View in: PubMed   Mentions: 220     Fields:    Translation:AnimalsCells
    33. A focused and efficient genetic screening strategy in the mouse: identification of mutations that disrupt cortical development. PLoS Biol. 2004 Aug; 2(8):E219. Zarbalis K, May SR, Shen Y, Ekker M, Rubenstein JL, Peterson AS. PMID: 15314648; PMCID: PMC509294.
      View in: PubMed   Mentions: 57     Fields:    Translation:AnimalsCells
    34. Multiple roles of ephrins during the formation of thalamocortical projections: maps and more. J Neurobiol. 2004 Apr; 59(1):82-94. Bolz J, Uziel D, Mühlfriedel S, Güllmar A, Peuckert C, Zarbalis K, Wurst W, Torii M, Levitt P. PMID: 15007829.
      View in: PubMed   Mentions: 28     Fields:    Translation:AnimalsCells
    35. Miswiring of limbic thalamocortical projections in the absence of ephrin-A5. J Neurosci. 2002 Nov 01; 22(21):9352-7. Uziel D, Mühlfriedel S, Zarbalis K, Wurst W, Levitt P, Bolz J. PMID: 12417660; PMCID: PMC6758033.
      View in: PubMed   Mentions: 18     Fields:    Translation:AnimalsCells
    36. A role for the EphA family in the topographic targeting of vomeronasal axons. Development. 2001 Mar; 128(6):895-906. Knöll B, Zarbalis K, Wurst W, Drescher U. PMID: 11222144.
      View in: PubMed   Mentions: 41     Fields:    Translation:AnimalsCells
    37. Expression domains of murine ephrin-A5 in the pituitary and hypothalamus. Mech Dev. 2000 May; 93(1-2):165-8. Zarbalis K, Wurst W. PMID: 10781950.
      View in: PubMed   Mentions: 15     Fields:    Translation:Animals
    38. Sequence analysis of the beta B2-crystallin cDNA of hamster containing a domain conserved among vertebrates. Gene. 1996 Sep 26; 174(1):181-4. Zarbalis K, Chatterjee B, Löster J, Werner T, Graw J. PMID: 8863746.
      View in: PubMed   Mentions:    Fields:    Translation:HumansAnimalsCells
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