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Alexander R. Paciorkowski, M.D.

Neurology, Pediatrics

Publications

Showing all 57 journal articles & 2 books available

Journal Articles

11/17/2017
Lee BH, Reijnders MRF, Abubakare O, Tuttle E, Lape B, Minks KQ, Stodgell C, Bennetto L, Kwon J, Fong CT, Gripp KW, Marsh ED, Smith WE, Huq AM, Coury SA, Tan WH, Solis O, Mehta RI, Leventer RJ, Baralle D, Hunt D, Paciorkowski AR. "Expanding the neurodevelopmental phenotype of PURA syndrome." American journal of medical genetics. Part A.. 2017 Nov 17; Epub 2017 Nov 17.

8/2017
Paciorkowski AR. "Congenital Zika syndrome: an epidemic of neurologic disability." Arquivos de neuro-psiquiatria.. 2017 Aug 0; 75(8):605.

6/27/2017
Zhang JF, James F, Shukla A, Girisha KM, Paciorkowski AR. "India Allele Finder: a web-based annotation tool for identifying common alleles in next-generation sequencing data of Indian origin." BMC research notes. 2017 Jun 27; 10(1):233. Epub 2017 Jun 27.

6/2017
Garavelli L, Ivanovski I, Caraffi SG, Santodirocco D, Pollazzon M, Cordelli DM, Abdalla E, Accorsi P, Adam MP, Baldo C, Bayat A, Belligni E, Bonvicini F, Breckpot J, Callewaert B, Cocchi G, Cuturilo G, Devriendt K, Dinulos MB, Djuric O, Epifanio R, Faravelli F, Formisano D, Giordano L, Grasso M, Grønborg S, Iodice A, Iughetti L, Lacombe D, Maggi M, Malbora B, Mammi I, Moutton S, Møller R, Muschke P, Napoli M, Pantaleoni C, Pascarella R, Pellicciari A, Poch-Olive ML, Raviglione F, Rivieri F, Russo C, Savasta S, Scarano G, Selicorni A, Silengo M, Sorge G, Tarani L, Tone LG, Toutain A, Trimouille A, Valera ET, Vergano SS, Zanotta N, Zollino M, Dobyns WB, Paciorkowski AR. "Neuroimaging findings in Mowat-Wilson syndrome: a study of 54 patients." Genetics in medicine : official journal of the American College of Medical Genetics.. 2017 Jun 0; 19(6):691-700. Epub 2016 Nov 10.

5/2/2017
Park K, Seltzer LE, Tuttle E, Mirzaa GM, Paciorkowski AR. "PLXNA1 developmental encephalopathy with syndromic features: A case report and review of the literature." American journal of medical genetics. Part A.. 2017 May 2; Epub 2017 May 02.

3/2017
Olson HE, Kelly M, LaCoursiere CM, Pinsky R, Tambunan D, Shain C, Ramgopal S, Takeoka M, Libenson MH, Julich K, Loddenkemper T, Marsh ED, Segal D, Koh S, Salman MS, Paciorkowski AR, Yang E, Bergin AM, Sheidley BR, Poduri A. "Genetics and genotype-phenotype correlations in early onset epileptic encephalopathy with burst suppression." Annals of neurology.. 2017 Mar 0; 81(3):419-429. Epub 2017 Feb 14.

2/9/2017
Traitruengsakul S, Seltzer LE, Paciorkowski AR, Ghoraani B. "Developing a novel epileptic discharge localization algorithm for electroencephalogram infantile spasms during hypsarrhythmia." Medical & biological engineering & computing.. 2017 Feb 9; Epub 2017 Feb 09.

2/2017
Pröschel C, Hansen JN, Ali A, Tuttle E, Lacagnina M, Buscaglia G, Halterman MW, Paciorkowski AR. "Epilepsy-causing sequence variations in SIK1 disrupt synaptic activity response gene expression and affect neuronal morphology." European journal of human genetics : EJHG.. 2017 Feb 0; 25(2):216-221. Epub 2016 Dec 14.

2017
Hsu T, Coughlin CC, Monaghan KG, Fiala E, McKinstry RC, Paciorkowski AR, Shinawi M. "CEDNIK: Phenotypic and Molecular Characterization of an Additional Patient and Review of the Literature." Child neurology open.. 2017 4:2329048X17733214. Epub 2017 Oct 08.

11/2016
Ma M, Adams HR, Seltzer LE, Dobyns WB, Paciorkowski AR. "Phenotype Differentiation of FOXG1 and MECP2 Disorders: A New Method for Characterization of Developmental Encephalopathies." The Journal of pediatrics.. 2016 Nov 0; 178:233-240.e10. Epub 2016 Sep 15.

5/10/2016
Papandreou A, Schneider RB, Augustine EF, Ng J, Mankad K, Meyer E, McTague A, Ngoh A, Hemingway C, Robinson R, Varadkar SM, Kinali M, Salpietro V, O'Driscoll MC, Basheer SN, Webster RI, Mohammad SS, Pula S, McGowan M, Trump N, Jenkins L, Elmslie F, Scott RH, Hurst JA, Perez-Duenas B, Paciorkowski AR, Kurian MA. "Delineation of the movement disorders associated with FOXG1 mutations." Neurology.. 2016 May 10; 86(19):1794-800. Epub 2016 Mar 30.

2/18/2016
Lugar HM, Koller JM, Rutlin J, Marshall BA, Kanekura K, Urano F, Bischoff AN, Shimony JS, Hershey T, . "Neuroimaging evidence of deficient axon myelination in Wolfram syndrome." Scientific reports.. 2016 Feb 18; 6:21167. Epub 2016 Feb 18.

12/2015
Morris CA, Mervis CB, Paciorkowski AP, Abdul-Rahman O, Dugan SL, Rope AF, Bader P, Hendon LG, Velleman SL, Klein-Tasman BP, Osborne LR. "7q11.23 Duplication syndrome: Physical characteristics and natural history." American journal of medical genetics. Part A.. 2015 Dec 0; 167A(12):2916-35. Epub 2015 Sep 03.

12/2015
McMahon KQ, Papandreou A, Ma M, Barry BJ, Mirzaa GM, Dobyns WB, Scott RH, Trump N, Kurian MA, Paciorkowski AR. "Familial recurrences of FOXG1-related disorder: Evidence for mosaicism." American journal of medical genetics. Part A.. 2015 Dec 0; 167A(12):3096-102. Epub 2015 Sep 14.

8/2015
Selioutski O, Seltzer LE, Burchfiel J, Paciorkowski AR, Erba G. "Characteristic Features of the Interictal EEG Background in 2 Patients With Malignant Migrating Partial Epilepsy in Infancy." Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society.. 2015 Aug 0; 32(4):e23-9.

6/2015
Lee BH, Smith T, Paciorkowski AR. "Autism spectrum disorder and epilepsy: Disorders with a shared biology." Epilepsy & behavior : E&B.. 2015 Jun 0; 47:191-201. Epub 2015 Apr 19.

5/30/2015
Bischoff AN, Reiersen AM, Buttlaire A, Al-Lozi A, Doty T, Marshall BA, Hershey T, . "Selective cognitive and psychiatric manifestations in Wolfram Syndrome." Orphanet journal of rare diseases. 2015 May 30; 10:66. Epub 2015 May 30.

4/2/2015
Hansen J, Snow C, Tuttle E, Ghoneim DH, Yang CS, Spencer A, Gunter SA, Smyser CD, Gurnett CA, Shinawi M, Dobyns WB, Wheless J, Halterman MW, Jansen LA, Paschal BM, Paciorkowski AR. "De novo mutations in SIK1 cause a spectrum of developmental epilepsies." American journal of human genetics.. 2015 Apr 2; 96(4):682-90.

3/2015
Paciorkowski AR, McDaniel SS, Jansen LA, Tully H, Tuttle E, Ghoneim DH, Tupal S, Gunter SA, Vasta V, Zhang Q, Tran T, Liu YB, Ozelius LJ, Brashear A, Sweadner KJ, Dobyns WB, Hahn S. "Novel mutations in ATP1A3 associated with catastrophic early life epilepsy, episodic prolonged apnea, and postnatal microcephaly." Epilepsia.. 2015 Mar 0; 56(3):422-30. Epub 2015 Feb 05.

2015
Traitruengsakul S, Seltzer LE, Paciorkowski AR, Ghoraani B. "Automatic localization of epileptic spikes in eegs of children with infantile spasms." Conference proceedings : ... Annual International Conference of the IEEE Engineering in Medicine and Biology Society.. 2015 2015:6194-7.

12/1/2014
Ghoneim DH, Myers JR, Tuttle E, Paciorkowski AR. "Comparison of insertion/deletion calling algorithms on human next-generation sequencing data." BMC research notes. 2014 Dec 1; 7:864. Epub 2014 Dec 01.

10/2014
Hoekel J, Chisholm SA, Al-Lozi A, Hershey T, Tychsen L, . "Ophthalmologic correlates of disease severity in children and adolescents with Wolfram syndrome." Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus. 2014 Oct 0; 18(5):461-465.e1. Epub 2014 Oct 21.

8/2014
Mirzaa GM, Vitre B, Carpenter G, Abramowicz I, Gleeson JG, Paciorkowski AR, Cleveland DW, Dobyns WB, O'Driscoll M. "Mutations in CENPE define a novel kinetochore-centromeric mechanism for microcephalic primordial dwarfism." Human genetics.. 2014 Aug 0; 133(8):1023-39. Epub 2014 Apr 20.

8/2014
Seltzer LE, Ma M, Ahmed S, Bertrand M, Dobyns WB, Wheless J, Paciorkowski AR. "Epilepsy and outcome in FOXG1-related disorders." Epilepsia.. 2014 Aug 0; 55(8):1292-300. Epub 2014 May 16.

6/2014
Mirzaa GM, Millen KJ, Barkovich AJ, Dobyns WB, Paciorkowski AR. "The Developmental Brain Disorders Database (DBDB): a curated neurogenetics knowledge base with clinical and research applications." American journal of medical genetics. Part A.. 2014 Jun 0; 164A(6):1503-11. Epub 2014 Apr 03.

6/2014
Seltzer LE, Paciorkowski AR. "Genetic disorders associated with postnatal microcephaly." American journal of medical genetics. Part C, Seminars in medical genetics.. 2014 Jun 0; 166C(2):140-55. Epub 2014 May 16.

6/2014
Mirzaa GM, Paciorkowski AR. "Introduction: Brain malformations." American journal of medical genetics. Part C, Seminars in medical genetics.. 2014 Jun 0; 166C(2):117-23. Epub 2014 May 22.

5/2014
Paciorkowski AR, Weisenberg J, Kelley JB, Spencer A, Tuttle E, Ghoneim D, Thio LL, Christian SL, Dobyns WB, Paschal BM. "Autosomal recessive mutations in nuclear transport factor KPNA7 are associated with infantile spasms and cerebellar malformation." European journal of human genetics : EJHG.. 2014 May 0; 22(5):587-93. Epub 2013 Sep 18.

4/3/2014
Cushion TD, Paciorkowski AR, Pilz DT, Mullins JG, Seltzer LE, Marion RW, Tuttle E, Ghoneim D, Christian SL, Chung SK, Rees MI, Dobyns WB. "De novo mutations in the beta-tubulin gene TUBB2A cause simplified gyral patterning and infantile-onset epilepsy." American journal of human genetics.. 2014 Apr 3; 94(4):634-41.

2014
Dubchak I, Balasubramanian S, Wang S, Meyden C, Sulakhe D, Poliakov A, Börnigen D, Xie B, Taylor A, Ma J, Paciorkowski AR, Mirzaa GM, Dave P, Agam G, Xu J, Al-Gazali L, Mason CE, Ross ME, Maltsev N, Gilliam TC. "An integrative computational approach for prioritization of genomic variants." PloS one. 2014 9(12):e114903. Epub 2014 Dec 15.

7/2013
Paciorkowski AR, Keppler-Noreuil K, Robinson L, Sullivan C, Sajan S, Christian SL, Bukshpun P, Gabriel SB, Gleeson JG, Sherr EH, Dobyns WB. "Deletion 16p13.11 uncovers NDE1 mutations on the non-deleted homolog and extends the spectrum of severe microcephaly to include fetal brain disruption." American journal of medical genetics. Part A.. 2013 Jul 0; 161A(7):1523-30. Epub 2013 May 23.

5/2013
Paciorkowski AR, Traylor RN, Rosenfeld JA, Hoover JM, Harris CJ, Winter S, Lacassie Y, Bialer M, Lamb AN, Schultz RA, Berry-Kravis E, Porter BE, Falk M, Venkat A, Vanzo RJ, Cohen JS, Fatemi A, Dobyns WB, Shaffer LG, Ballif BC, Marsh ED. "MEF2C Haploinsufficiency features consistent hyperkinesis, variable epilepsy, and has a role in dorsal and ventral neuronal developmental pathways." Neurogenetics.. 2013 May 0; 14(2):99-111. Epub 2013 Feb 07.

5/2013
McDonell LM, Mirzaa GM, Alcantara D, Schwartzentruber J, Carter MT, Lee LJ, Clericuzio CL, Graham JM, Morris-Rosendahl DJ, Polster T, Acsadi G, Townshend S, Williams S, Halbert A, Isidor B, David A, Smyser CD, Paciorkowski AR, Willing M, Woulfe J, Das S, Beaulieu CL, Marcadier J, , Geraghty MT, Frey BJ, Majewski J, Bulman DE, Dobyns WB, O'Driscoll M, Boycott KM. "Mutations in STAMBP, encoding a deubiquitinating enzyme, cause microcephaly-capillary malformation syndrome." Nature genetics.. 2013 May 0; 45(5):556-62. Epub 2013 Mar 31.

5/2013
Mirzaa GM, Paciorkowski AR, Marsh ED, Berry-Kravis EM, Medne L, Grix A, Wirrell EC, Powell BR, Nickels KC, Burton B, Paras A, Kim K, Chung W, Dobyns WB, Das S. "CDKL5 and ARX mutations in males with early-onset epilepsy." Pediatric neurology.. 2013 May 0; 48(5):367-77.

4/27/2013
Marshall BA, Permutt MA, Paciorkowski AR, Hoekel J, Karzon R, Wasson J, Viehover A, White NH, Shimony JS, Manwaring L, Austin P, Hullar TE, Hershey T, The Washington University Wolfram Study Group W. "Phenotypic characteristics of early Wolfram syndrome." Orphanet journal of rare diseases. 2013 Apr 27; 8:64. Epub 2013 Apr 27.

1/29/2013
Paciorkowski AR, Darras BT. "Making sense of genetic heterogeneity: Emergence of pathways in developmental brain disorders." Neurology.. 2013 Jan 29; 80(5):426-7. Epub 2013 Jan 02.

2013
Sajan SA, Fernandez L, Nieh SE, Rider E, Bukshpun P, Wakahiro M, Christian SL, Rivière JB, Sullivan CT, Sudi J, Herriges MJ, Paciorkowski AR, Barkovich AJ, Glessner JT, Millen KJ, Hakonarson H, Dobyns WB, Sherr EH. "Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyria." PLoS genetics.. 2013 9(10):e1003823. Epub 2013 Oct 03.

11/14/2012
Nguyen C, Foster ER, Paciorkowski AR, Viehoever A, Considine C, Bondurant A, Marshall BA, Hershey T. "Reliability and validity of the Wolfram Unified Rating Scale (WURS)." Orphanet journal of rare diseases. 2012 Nov 14; 7:89. Epub 2012 Nov 14.

7/2012
Pickett KA, Duncan RP, Paciorkowski AR, Permutt MA, Marshall B, Hershey T, Earhart GM, . "Balance impairment in individuals with Wolfram syndrome." Gait & posture.. 2012 Jul 0; 36(3):619-24. Epub 2012 Jul 06.

2/2012
Rosenfeld JA, Amrom D, Andermann E, Andermann F, Veilleux M, Curry C, Fisher J, Deputy S, Aylsworth AS, Powell CM, Manickam K, Heese B, Maisenbacher M, Stevens C, Ellison JW, Upton S, Moeschler J, Torres-Martinez W, Stevens A, Marion R, Pereira EM, Babcock M, Morrow B, Sahoo T, Lamb AN, Ballif BC, Paciorkowski AR, Shaffer LG. "Genotype-phenotype correlation in interstitial 6q deletions: a report of 12 new cases." Neurogenetics.. 2012 Feb 0; 13(1):31-47. Epub 2012 Jan 05.

1/2012
Stankiewicz P, Kulkarni S, Dharmadhikari AV, Sampath S, Bhatt SS, Shaikh TH, Xia Z, Pursley AN, Cooper ML, Shinawi M, Paciorkowski AR, Grange DK, Noetzel MJ, Saunders S, Simons P, Summar M, Lee B, Scaglia F, Fellmann F, Martinet D, Beckmann JS, Asamoah A, Platky K, Sparks S, Martin AS, Madan-Khetarpal S, Hoover J, Medne L, Bonnemann CG, Moeschler JB, Vallee SE, Parikh S, Irwin P, Dalzell VP, Smith WE, Banks VC, Flannery DB, Lovell CM, Bellus GA, Golden-Grant K, Gorski JL, Kussmann JL, McGregor TL, Hamid R, Pfotenhauer J, Ballif BC, Shaw CA, Kang SH, Bacino CA, Patel A, Rosenfeld JA, Cheung SW, Shaffer LG. "Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeats." Human mutation.. 2012 Jan 0; 33(1):165-79. Epub 2011 Nov 02.

2012
Hucthagowder V, Liu TC, Paciorkowski AR, Thio LL, Keller MS, Anderson CD, Herman T, Dehner LP, Grange DK, Kulkarni S. "Chromosome 2p15p16.1 microdeletion syndrome: 2.5 Mb deletion in a patient with renal anomalies, intractable seizures and a choledochal cyst." European journal of medical genetics.. 2012 55(8-9):485-9. Epub 2012 Apr 22.

2012
Hershey T, Lugar HM, Shimony JS, Rutlin J, Koller JM, Perantie DC, Paciorkowski AR, Eisenstein SA, Permutt MA, . "Early brain vulnerability in Wolfram syndrome." PloS one. 2012 7(7):e40604. Epub 2012 Jul 11.

12/2011
Paciorkowski AR, Thio LL, Rosenfeld JA, Gajecka M, Gurnett CA, Kulkarni S, Chung WK, Marsh ED, Gentile M, Reggin JD, Wheless JW, Balasubramanian S, Kumar R, Christian SL, Marini C, Guerrini R, Maltsev N, Shaffer LG, Dobyns WB. "Copy number variants and infantile spasms: evidence for abnormalities in ventral forebrain development and pathways of synaptic function." European journal of human genetics : EJHG.. 2011 Dec 0; 19(12):1238-45. Epub 2011 Jun 22.

12/2011
Paciorkowski AR, Thio LL, Dobyns WB. "Genetic and biologic classification of infantile spasms." Pediatric neurology.. 2011 Dec 0; 45(6):355-67.

9/15/2011
Lukashin I, Novichkov P, Boffelli D, Paciorkowski AR, Minovitsky S, Yang S, Dubchak I. "VISTA Region Viewer (RViewer)--a computational system for prioritizing genomic intervals for biomedical studies." Bioinformatics.. 2011 Sep 15; 27(18):2595-7. Epub 2011 Jul 26.

9/13/2011
Paciorkowski AR, Shafrir Y, Hrivnak J, Patterson MC, Tennison MB, Clark HB, Gomez CM. "Massive expansion of SCA2 with autonomic dysfunction, retinitis pigmentosa, and infantile spasms." Neurology.. 2011 Sep 13; 77(11):1055-60. Epub 2011 Aug 31.

9/2011
Mirzaa GM, Paciorkowski AR, Smyser CD, Willing MC, Lind AC, Dobyns WB. "The microcephaly-capillary malformation syndrome." American journal of medical genetics. Part A.. 2011 Sep 0; 155A(9):2080-7. Epub 2011 Aug 03.

1/2011
Brunetti-Pierri N, Paciorkowski AR, Ciccone R, Della Mina E, Bonaglia MC, Borgatti R, Schaaf CP, Sutton VR, Xia Z, Jelluma N, Ruivenkamp C, Bertrand M, de Ravel TJ, Jayakar P, Belli S, Rocchetti K, Pantaleoni C, D'Arrigo S, Hughes J, Cheung SW, Zuffardi O, Stankiewicz P. "Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairment." European journal of human genetics : EJHG.. 2011 Jan 0; 19(1):102-7. Epub 2010 Aug 25.

12/2009
Paciorkowski AR, Fang M. "Chromosomal microarray interpretation: what is a child neurologist to do?" Pediatric neurology.. 2009 Dec 0; 41(6):391-8.

3/24/2009
Klawiter EC, Alvarez E, Xu J, Paciorkowski AR, Zhu L, Parks BJ, Cross AH, Naismith RT. "NMO-IgG detected in CSF in seronegative neuromyelitis optica." Neurology.. 2009 Mar 24; 72(12):1101-3.

4/2008
Paciorkowski AR, Sathe S, Zeng BJ, Torres P, Rosengren SS, Kolodny E. "Juvenile-onset G(M2)-gangliosidosis in an African-American child with nystagmus." Pediatric neurology.. 2008 Apr 0; 38(4):284-6.

1/2008
Paciorkowski AR, Westwell M, Ounpuu S, Bell K, Kagan J, Mazzarella C, Greenstein RM. "Motion analysis of a child with Niemann-Pick disease type C treated with miglustat." Movement disorders : official journal of the Movement Disorder Society.. 2008 Jan 0; 23(1):124-8.

7/2007
Paciorkowski AR, Greenstein RM. "When is enlargement of the subarachnoid spaces not benign? A genetic perspective." Pediatric neurology.. 2007 Jul 0; 37(1):1-7.

6/2002
Paciorkowski AR, Lerer T, Brunquell PJ. "Structure-function correlations in patients with malformations of cortical development." Epilepsy & behavior : E&B.. 2002 Jun 0; 3(3):266-274.

10/1997
Paciorkowski A, Dai WW, Cerami A, Berger BJ. "Synergism of cimetidine with anti-malarial agents." The Journal of parasitology.. 1997 Oct 0; 83(5):960-3.

9/1996
Berger BJ, Paciorkowski A, Suskin M, Dai WW, Cerami A, Ulrich P. "Antimalarial activity of novel arylene bis(methylketone) compounds." The Journal of infectious diseases.. 1996 Sep 0; 174(3):659-62.

Books & Chapters

2017
Chapter Title: Developmental Encephalopathies.
Book Title: Swaiman's Pediatric Neurology, Principles and Practice. 6th Edition.
Author List: AR Paciorkowski, LE Seltzer, JL Neul.
Published By: Elsevier2017

2017
Chapter Title: Neurogenetics in the Genome Era.
Book Title: Swaiman's Pediatric Neurology, Principles and Practice. 6th Edition.
Author List: K McMahon, AR Paciorkowski, LC Walters-Sen, JM Milunsky, A Bassuk, B Darbro, J Diaz, WB Dobyns, A Gropman.
Published By: Elsevier2017