Publications by authors named "SG Ryan"

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T
Theranostic Near-Infrared-Active Conjugated Polymer Nanoparticles.
Miao Zhao, Edward Leggett, Struan Bourke, Souzana Poursanidou, Sadie Carter-Searjeant, Sean G Ryan

ACS Nano· May 2021

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Imaging of X-Ray-Excited Emissions from Quantum Dots and Biological Tissue in Whole Mouse.
Sean G Ryan, Matthew N Butler, Segun S Adeyemi, Tammy Kalber, P Stephen Patrick

Sci Rep· December 2019

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Nucleosynthetic signatures of the first stars.
Anna Frebel, Wako Aoki, Norbert Christlieb, Hiroyasu Ando, Martin Asplund, Sean G Ryan

Nature· April 2005

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Association between variation in the human KCNJ10 potassium ion channel gene and seizure susceptibility.
R J Buono, F W Lohoff, T Sander, M R Sperling, M J O'Connor, S G Ryan

Epilepsy Res· February 2004

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Pharmacogenetics and pharmacogenomics in drug development and regulatory decision making: report of the first FDA-PWG-PhRMA-DruSafe Workshop.
Lawrence J Lesko, Ronald A Salerno, Brian B Spear, Donald C Anderson, Timothy Anderson, Stephen G Ryan

J Clin Pharmacol· April 2003

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Regression to the truth: replication of association in pharmacogenetic studies.
Stephen G Ryan

Pharmacogenomics· March 2003

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Human genetic variation.
Stephen G Ryan

Pharmacogenomics· January 2002

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Lack of association between an interleukin 1 beta (IL-1beta) gene variation and refractory temporal lobe epilepsy.
R J Buono, T N Ferraro, M J O'Connor, M R Sperling, S G Ryan

Epilepsia· June 2001

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Medial medullary injury during adenoidectomy.
P B Kang, H K Phuah, R A Zimmerman, S D Handler, L S Dure, S G Ryan

J Pediatr· May 2001

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Detection of Lead in the Carbon-rich, Very Metal-poor Star LP 625-44: A Strong Constraint on s-Process Nucleosynthesis at Low Metallicity.
W Aoki, JE Norris, SG Ryan, TC Beers, H Ando

Astrophys J· June 2000

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Primordial Lithium and Big Bang Nucleosynthesis.
SG Ryan, TC Beers, KA Olive, BD Fields, JE Norris

Astrophys J· February 2000

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Genetic susceptibility to neurodevelopmental disorders.
S G Ryan

J Child Neurol· March 1999

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Ion channels and the genetic contribution to epilepsy.
S G Ryan

J Child Neurol· January 1999

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Linkage of the gene for an autosomal dominant form of juvenile amyotrophic lateral sclerosis to chromosome 9q34.
P F Chance, B A Rabin, S G Ryan, Y Ding, M Scavina

Am J Hum Genet· March 1998

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A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family.
C Charlier, N A Singh, S G Ryan, T B Lewis, B E Reus

Nat Genet· January 1998

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Epilepsy and mental retardation limited to females: an X-linked dominant disorder with male sparing.
S G Ryan, P F Chance, C H Zou, N B Spinner, J A Golden

Nat Genet· September 1997

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Evidence of a third locus for benign familial convulsions.
T B Lewis, M I Shevell, E Andermann, S G Ryan, R J Leach

J Child Neurol· May 1996

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Mutational analysis of familial and sporadic hyperekplexia.
R Shiang, S G Ryan, Y Z Zhu, T J Fielder, R J Allen

Ann Neurol· July 1995

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Partial epilepsy: chinks in the armour.
S G Ryan

Nat Genet· May 1995

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A missense mutation in the gene encoding the alpha 1 subunit of the inhibitory glycine receptor in the spasmodic mouse.
S G Ryan, M S Buckwalter, J W Lynch, C A Handford, L Segura

Nat Genet· June 1994

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Deletion 5q35.3.
R F Stratton, N A Tedrowe, J A Tolworthy, R M Patterson, S G Ryan

Am J Med Genet· June 1994

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Hyperekplexia associated with apnea and sudden infant death syndrome.
G P Giacoia, S G Ryan

Arch Pediatr Adolesc Med· May 1994

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Paroxysmal kinesigenic dystonia after methylphenidate administration.
C T Gay, S G Ryan

J Child Neurol· January 1994

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Mutations in the alpha 1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia.
R Shiang, S G Ryan, Y Z Zhu, A F Hahn, P O'Connell

Nat Genet· December 1993

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Genetic heterogeneity in benign familial neonatal convulsions: identification of a new locus on chromosome 8q.
T B Lewis, R J Leach, K Ward, P O'Connell, S G Ryan

Am J Hum Genet· September 1993

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