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Richard King

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Johanna M Dijkstal; Ann M Holleschau; Richard A King; San-San Cooley; C Gail Summers
Change in visual acuity in albinism in the early school years.
William S Oetting; Jacy Pietsch; Marcia J Brott; Sarah Savage; James P Fryer; C Gail Summers; Richard A King
The R402Q tyrosinase variant does not cause autosomal recessive ocular albinism.
Jagadish Patil; Jeffrey D Lande; Na Li; Todd R Berryman; Richard A King; Marshall I Hertz
Bronchoalveolar lavage cell gene expression in acute lung rejection: development of a diagnostic classifier.

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2012: Johanna M Dijkstal; Ann M Holleschau; Richard A King; San-San Cooley; C Gail Summers
Change in visual acuity in albinism in the early school years.
Journal of pediatric ophthalmology and strabismus 2012;49(2):81-6; quiz 87.
2009: William S Oetting; Jacy Pietsch; Marcia J Brott; Sarah Savage; James P Fryer; C Gail Summers; Richard A King
The R402Q tyrosinase variant does not cause autosomal recessive ocular albinism.
American journal of medical genetics. Part A 2009;149A(3):466-9.
2008: Jagadish Patil; Jeffrey D Lande; Na Li; Todd R Berryman; Richard A King; Marshall I Hertz
Bronchoalveolar lavage cell gene expression in acute lung rejection: development of a diagnostic classifier.
Transplantation 2008;85(2):224-31.
2007: Beth Kutzbach; C Gail Summers; Ann M Holleschau; Richard A King; John T MacDonald
The prevalence of attention-deficit/hyperactivity disorder among persons with albinism.
Journal of child neurology 2007;22(12):1342-7.
2007: Jeffrey D Lande; Jagadish Patil; Na Li; Todd R Berryman; Richard A King; Marshall I Hertz
Novel insights into lung transplant rejection by microarray analysis.
Proceedings of the American Thoracic Society 2007;4(1):44-51.
2006: Patti S Harvey; Richard A King; C Gail Summers
Spectrum of foveal development in albinism detected with optical coherence tomography.
Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus / American Association for Pediatric Ophthalmology and Strabismus 2006;10(3):237-42.
2006: Curtis R Louwagie; Allison A Jensen; Alexander Christoff; Ann M Holleschau; Richard A King; C Gail Summers
Correlation of grating acuity with letter recognition acuity in children with albinism.
Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus / American Association for Pediatric Ophthalmology and Strabismus 2006;10(2):168-72.
2006: Malcolm N Blumenthal; Carl D Langefeld; Kathleen C Barnes; Carole Ober; Deborah A Meyers; Richard A King; Terri H beaty; Stephanie R Beck; Eugene R Bleecker; Stephen S Rich
A genome-wide search for quantitative trait loci contributing to variation in seasonal pollen reactivity.
The Journal of allergy and clinical immunology 2006;117(1):79-85.
2005: Jeffrey D Lande; Stacy L Dalheimer; Daniel L Mueller; Marshall I Hertz; Richard A King
Gene expression profiling in murine obliterative airway disease.
American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons 2005;5(9):2170-84.
2005: William S Oetting; Sarah Savage Garrett; Marcia J Brott; Richard A King
P gene mutations associated with oculocutaneous albinism type II (OCA2).
Human mutation 2005;25(3):323.
2004: C Gail Summers; Richard A King; Kimberly S Merrill; Jane D Lavoie
Positive angle kappa in albinism.
American journal of ophthalmology 2004;138(6):1093.
2004: Jill Anderson; Jane Lavoie; Kimberly S Merrill; Richard A King; C Gail Summers
Efficacy of spectacles in persons with albinism.
Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus / American Association for Pediatric Ophthalmology and Strabismus 2004;8(6):515-20.
2004: Kimberly S Merrill; Jane D Lavoie; Richard A King; C Gail Summers
Positive angle kappa in albinism.
Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus / American Association for Pediatric Ophthalmology and Strabismus 2004;8(3):237-9.
2004: Terri L Young; Samir S Deeb; Shawn M Ronan; Andrew T DeWan; Alison B Alvear; Genaro S Scavello; Prasuna Paluru; Marcia S Brott; Takaaki Hayashi; Ann M Holleschau; Nancy Benegas; Marianne Schwartz; Larry D Atwood; William S Oetting; Thomas Rosenberg; Arno G Motulsky; Richard A King
X-linked high myopia associated with cone dysfunction.
Archives of ophthalmology 2004;122(6):897-908.
2004: Malcolm N Blumenthal; Carole Ober; Terri H beaty; Eugene R Bleecker; Carl D Langefeld; Richard A King; Lucille A Lester; N Cox; Kathleen C Barnes; Alkis Togias; Rasika A Mathias; Deborah A Meyers; William S Oetting; Stephen S Rich
Genome scan for loci linked to mite sensitivity: the Collaborative Study on the Genetics of Asthma (CSGA).
Genes and immunity 2004;5(3):226-31.
2004: Malcolm N Blumenthal; Carl D Langefeld; Terri H beaty; Eugene R Bleecker; Carole Ober; Lucille A Lester; Ethan M Lange; Kathleen C Barnes; Raoul Wolf; Richard A King; Julian Solway; William S Oetting; Deborah A Meyers; Stephen S Rich
A genome-wide search for allergic response (atopy) genes in three ethnic groups: Collaborative Study on the Genetics of Asthma.
Human genetics 2004;114(2):157-64.
2003: James P Fryer; William S Oetting; Richard A King
Identification and characterization of a DNase hypersensitive region of the human tyrosinase gene.
Pigment cell research / sponsored by the European Society for Pigment Cell Research and the International Pigment Cell Society 2003;16(6):679-84.
2003: Vincent J Gimino; Jeffrey D Lande; Todd R Berryman; Richard A King; Marshall I Hertz
Gene expression profiling of bronchoalveolar lavage cells in acute lung rejection.
American journal of respiratory and critical care medicine 2003;168(10):1237-42.
2003: Richard A King; Jacy Pietsch; James P Fryer; Sarah Savage; Marcia J Brott; Isabelle Russell-Eggitt; C Gail Summers; William S Oetting
Tyrosinase gene mutations in oculocutaneous albinism 1 (OCA1): definition of the phenotype.
Human genetics 2003;113(6):502-13.
2003: Terri L Young; Xiaoshan D Guo; Richard A King; Janell M Johnson; Jody A Rada
Identification of genes expressed in a human scleral cDNA library.
Molecular vision 2003;9():508-14.
2003: Richard A King; Rebecca K Willaert; Ramona M Schmidt; Jacy Pietsch; Sarah Savage; Marcia J Brott; James P Fryer; C Gail Summers; William S Oetting
MC1R mutations modify the classic phenotype of oculocutaneous albinism type 2 (OCA2).
American journal of human genetics 2003;73(3):638-45.
2003: William S Oetting; James P Fryer; Sabitha Shriram; Richard A King
Oculocutaneous albinism type 1: the last 100 years.
Pigment cell research / sponsored by the European Society for Pigment Cell Research and the International Pigment Cell Society 2003;16(3):307-11.
2003: Prasuna Paluru; Shawn M Ronan; Elise Heon; Marcella Devoto; Scott C Wildenberg; Genaro S Scavello; Ann M Holleschau; Outi Mäkitie; William G Cole; Richard A King; Terri L Young
New locus for autosomal dominant high myopia maps to the long arm of chromosome 17.
Investigative ophthalmology & visual science 2003;44(5):1830-6.
2003: Zanhua Yi; Nanibaa' Garrison; Orit Cohen-Barak; Tatiana M Karafet; Richard A King; Robert P Erickson; Michael F Hammer; Murray H Brilliant
A 122.5-kilobase deletion of the P gene underlies the high prevalence of oculocutaneous albinism type 2 in the Navajo population.
American journal of human genetics 2003;72(1):62-72.
2001: James P Fryer; William S Oetting; Marcia J Brott; Richard A King
Alternative splicing of the tyrosinase gene transcript in normal human melanocytes and lymphocytes.
The Journal of investigative dermatology 2001;117(5):1261-5.
2001: J M Newton; Orit Cohen-Barak; Nobuko Hagiwara; JM Gardner; Muriel T Davisson; Richard A King; Murray H Brilliant
Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4.
American journal of human genetics 2001;69(5):981-8.
2001: Terri L Young; Larry D Atwood; Shawn M Ronan; Andrew T DeWan; Alison B Alvear; J Peterson; Ann M Holleschau; Richard A King
Further refinement of the MYP2 locus for autosomal dominant high myopia by linkage disequilibrium analysis.
Ophthalmic genetics 2001;22(2):69-75.
2001: Jianfeng Xu; Deborah A Meyers; Carole Ober; Malcolm N Blumenthal; Beverly G Mellen; Kathleen C Barnes; Richard A King; Lucille A Lester; Timothy Howard; Julian Solway; Carl D Langefeld; Terri H beaty; Stephen S Rich; Eugene R Bleecker; Nancy J Cox
Genomewide screen and identification of gene-gene interactions for asthma-susceptibility loci in three U.S. populations: collaborative study on the genetics of asthma.
American journal of human genetics 2001;68(6):1437-46.
2001: K A Lee; Richard A King; C Gail Summers
Stereopsis in patients with albinism: clinical correlates.
Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus / American Association for Pediatric Ophthalmology and Strabismus 2001;5(2):98-104.
2000: Carole Ober; S A Leavitt; Anya Tsalenko; Timothy Howard; DM Hoki; R Daniel; Dina L Newman; Xiaodong Wu; Rodney Parry; Lucille A Lester; Julian Solway; Malcolm N Blumenthal; Richard A King; Jianfeng Xu; Deborah A Meyers; Eugene R Bleecker; Nancy J Cox
Variation in the interleukin 4-receptor alpha gene confers susceptibility to asthma and atopy in ethnically diverse populations.
American journal of human genetics 2000;66(2):517-26.
1999: William S Oetting; Richard A King
Molecular basis of albinism: mutations and polymorphisms of pigmentation genes associated with albinism.
Human mutation 1999;13(2):99-115.
1998: William S Oetting; C M Armstrong; Shawn M Ronan; Terri L Young; T A Sellers; Richard A King
Multiplexed short tandem repeat polymorphisms of the Weber 8A set of markers using tailed primers and infrared fluorescence detection.
Electrophoresis 1998;19(18):3079-83.
1998: Terri L Young; Shawn M Ronan; Alison B Alvear; Scott C Wildenberg; William S Oetting; Larry D Atwood; D J Wilkin; Richard A King
A second locus for familial high myopia maps to chromosome 12q.
American journal of human genetics 1998;63(5):1419-24.
1998: Terri L Young; Shawn M Ronan; L A Drahozal; Scott C Wildenberg; Alison B Alvear; William S Oetting; Larry D Atwood; D J Wilkin; Richard A King
Evidence that a locus for familial high myopia maps to chromosome 18p.
American journal of human genetics 1998;63(1):109-19.
1998: Scott C Wildenberg; James P Fryer; JM Gardner; William S Oetting; Murray H Brilliant; Richard A King
Identification of a novel transcript produced by the gene responsible for the Hermansky-Pudlak syndrome in Puerto Rico.
The Journal of investigative dermatology 1998;110(5):777-81.
1998: William S Oetting; JM Gardner; James P Fryer; A Ching; D Durham-Pierre; Richard A King; Murray H Brilliant
Mutations of the human P gene associated with Type II oculocutaneous albinism (OCA2). Mutations in brief no. 205. Online.
Human mutation 1998;12(6):434.
1998: William S Oetting; James P Fryer; Richard A King
Mutations of the human tyrosinase gene associated with tyrosinase related oculocutaneous albinism (OCA1). Mutations in brief no. 204. Online.
Human mutation 1998;12(6):433-4.
1997: N Puri; D Durbam-Pierre; R Aquaron; P M Lund; Richard A King; Murray H Brilliant
Type 2 oculocutaneous albinism (OCA2) in Zimbabwe and Cameroon: distribution of the 2.7-kb deletion allele of the P gene.
Human genetics 1997;100(5-6):651-6.
1997: P M Lund; N Puri; D Durham-Pierre; Richard A King; Murray H Brilliant
Oculocutaneous albinism in an isolated Tonga community in Zimbabwe.
Journal of medical genetics 1997;34(9):733-5.
1997: JM Gardner; Scott C Wildenberg; N M Keiper; Edward K Novak; Michael E Rusiniak; Richard T Swank; N Puri; J N Finger; Nobuko Hagiwara; AL Lehman; TL Gales; M E Bayer; Richard A King; Murray H Brilliant
The mouse pale ear (ep) mutation is the homologue of human Hermansky-Pudlak syndrome.
Proceedings of the National Academy of Sciences of the United States of America 1997;94(17):9238-43.
1996: William S Oetting; Murray H Brilliant; Richard A King
The clinical spectrum of albinism in humans.
Molecular medicine today 1996;2(8):330-5.
1996: Raymond E Boissy; H Zhao; William S Oetting; L M Austin; Scott C Wildenberg; Y L Boissy; Y Zhao; R A Sturm; Vincent J Hearing; Richard A King; James J Nordlund
Mutation in and lack of expression of tyrosinase-related protein-1 (TRP-1) in melanocytes from an individual with brown oculocutaneous albinism: a new subtype of albinism classified as "OCA3".
American journal of human genetics 1996;58(6):1145-56.
1996: C Gail Summers; William S Oetting; Richard A King
Diagnosis of oculocutaneous albinism with molecular analysis.
American journal of ophthalmology 1996;121(6):724-6.
1996: D Durham-Pierre; Richard A King; J M Naber; S Laken; Murray H Brilliant
Estimation of carrier frequency of a 2.7 kb deletion allele of the P gene associated with OCA2 in African-Americans.
Human mutation 1996;7(4):370-3.
1995: William S Oetting; H K Lee; D J Flanders; G L Wiesner; T A Sellers; Richard A King
Linkage analysis with multiplexed short tandem repeat polymorphisms using infrared fluorescence and M13 tailed primers.
Genomics 1995;30(3):450-8.
1995: Scott C Wildenberg; William S Oetting; C Almodóvar; M Krumwiede; J G White; Richard A King
A gene causing Hermansky-Pudlak syndrome in a Puerto Rican population maps to chromosome 10q2.
American journal of human genetics 1995;57(4):755-65.
1995: Scott C Wildenberg; Richard A King; William S Oetting
Detection of a Tsp509I polymorphism in the 3' UTR of the human tyrosinase related protein-1 (TYRP) gene.
Human genetics 1995;95(2):247.
1994: William S Oetting; Richard A King
Molecular basis of oculocutaneous albinism.
The Journal of investigative dermatology 1994;103(5 Suppl):131S-136S.
1994: William S Oetting; Richard A King
Analysis of tyrosinase mutations associated with tyrosinase-related oculocutaneous albinism (OCA1).
Pigment cell research / sponsored by the European Society for Pigment Cell Research and the International Pigment Cell Society 1994;7(5):285-90.
1994: H Zhao; Y L Boissy; Zalfa A Abdel-Malek; Richard A King; James J Nordlund; Raymond E Boissy
On the analysis of the pathophysiology of Chediak-Higashi syndrome. Defects expressed by cultured melanocytes.
Laboratory investigation; a journal of technical methods and pathology 1994;71(1):25-34.
1994: D Durham-Pierre; JM Gardner; Y Nakatsu; Richard A King; U Francke; A Ching; R Aquaron; V del Marmol; Murray H Brilliant
African origin of an intragenic deletion of the human P gene in tyrosinase positive oculocutaneous albinism.
Nature genetics 1994;7(2):176-9.
1994: C Gail Summers; Richard A King
Ophthalmic features of minimal pigment oculocutaneous albinism.
Ophthalmology 1994;101(5):906-14.
1994: K R Harmon; C J Witkop; J G White; Richard A King; M Peterson; D Moore; J Tashjian; W A Marinelli; P B Bitterman
Pathogenesis of pulmonary fibrosis: platelet-derived growth factor precedes structural alterations in the Hermansky-Pudlak syndrome.
The Journal of laboratory and clinical medicine 1994;123(4):617-27.
1994: William S Oetting; James P Fryer; Y Oofuji; L R Middendorf; J A Brumbaugh; C Gail Summers; Richard A King
Analysis of tyrosinase gene mutations using direct automated infrared fluorescence DNA sequencing of amplified exons.
Electrophoresis 1994;15(2):159-64.
1994: William S Oetting; C Gail Summers; Richard A King
Albinism and the associated ocular defects.
Metabolic, pediatric, and systemic ophthalmology (New York, N.Y. : 1985) 1994;17(1-4):5-9.
1993: William S Oetting; James P Fryer; Richard A King
A dinucleotide deletion (-delta GA115) in the tyrosinase gene responsible for type I-A (tyrosinase negative) oculocutaneous albinism in a Pakistani individual.
Human molecular genetics 1993;2(7):1047-8.
1993: William S Oetting; O Colin Stine; D Townsend; Richard A King
Evolution of the tyrosinase related gene (TYRL) in primates.
Pigment cell research / sponsored by the European Society for Pigment Cell Research and the International Pigment Cell Society 1993;6(3):171-7.
1993: Richard A King; G L Wiesner; D Townsend; J G White
Hypopigmentation in Angelman syndrome.
American journal of medical genetics 1993;46(1):40-4.
1993: William S Oetting; Richard A King
Molecular basis of type I (tyrosinase-related) oculocutaneous albinism: mutations and polymorphisms of the human tyrosinase gene.
Human mutation 1993;2(1):1-6.
1993: William S Oetting; C J Witkop; S A Brown; R Colomer; James P Fryer; K E Bloom; Richard A King
A frequent tyrosinase gene mutation associated with type I-A (tyrosinase-negative) oculocutaneous albinism in Puerto Rico.
American journal of human genetics 1993;52(1):17-23.
1992: William S Oetting; Richard A King
Molecular analysis of type I-A (tyrosinase negative) oculocutaneous albinism.
Human genetics 1992;90(3):258-62.
1992: William S Oetting; Richard A King
Analysis of mutations in the copper B binding region associated with type I (tyrosinase-related) oculocutaneous albinism.
Pigment cell research / sponsored by the European Society for Pigment Cell Research and the International Pigment Cell Society 1992;5(5 Pt 2):274-8.
1992: JM Gardner; Y Nakatsu; Y Gondo; S Lee; Mary F Lyon; Richard A King; Murray H Brilliant
The mouse pink-eyed dilution gene: association with human Prader-Willi and Angelman syndromes.
Science (New York, N.Y.) 1992;257(5073):1121-4.
1992: D Townsend; William S Oetting; T Polman; Richard A King
Purification and characterization of dopachrome tautomerase (DT).
Pigment cell research / sponsored by the European Society for Pigment Cell Research and the International Pigment Cell Society 1992;Suppl 2():32-5.
1992: Richard A King; William S Oetting
Molecular basis of type IA (tyrosinase negative) oculocutaneous albinism.
Pigment cell research / sponsored by the European Society for Pigment Cell Research and the International Pigment Cell Society 1992;Suppl 2():249-53.
1991: William S Oetting; C M Roed; Margaret M Mentink-Kane; Richard A King
PCR detection of a TaqI polymorphism at the CCAATT box of the human tyrosinase (TYR) gene.
Nucleic acids research 1991;19(20):5800.
1991: C Gail Summers; D Creel; D Townsend; Richard A King
Variable expression of vision in sibs with albinism.
American journal of medical genetics 1991;40(3):327-31.
1991: William S Oetting; Margaret M Mentink-Kane; C Gail Summers; R A Lewis; J G White; Richard A King
Three different frameshift mutations of the tyrosinase gene in type IA oculocutaneous albinism.
American journal of human genetics 1991;49(1):199-206.
1991: William S Oetting; H Y Handoko; Margaret M Mentink-Kane; A S Paller; J G White; Richard A King
Molecular analysis of an extended family with type IA (tyrosinase-negative) oculocutaneous albinism.
The Journal of investigative dermatology 1991;97(1):15-9.
1991: Richard A King; D Townsend; William S Oetting; C Gail Summers; D P Olds; J G White; R A Spritz
Temperature-sensitive tyrosinase associated with peripheral pigmentation in oculocutaneous albinism.
The Journal of clinical investigation 1991;87(3):1046-53.
1991: Richard A King; Margaret M Mentink-Kane; William S Oetting
Non-random distribution of missense mutations within the human tyrosinase gene in type I (tyrosinase-related) oculocutaneous albinism.
Molecular biology & medicine 1991;8(1):19-29.
1990: C J Witkop; M Nuñez Babcock; G H Rao; F Gaudier; C Gail Summers; F Shanahan; K R Harmon; D Townsend; H O Sedano; Richard A King
Albinism and Hermansky-Pudlak syndrome in Puerto Rico.
Boletín de la Asociación Médica de Puerto Rico 1990;82(8):333-9.
1988: B S LeRoy; N A Uhrhammer; K J Steere; Corinne D Boehm; Richard A King; S S Rich; P P Williams; S A Smith; B de Martinville
Identification of carriers of Duchenne muscular dystrophy: value of molecular analysis.
American journal of medical genetics 1988;31(3):709-21.
1988: Richard A King; C Gail Summers
Albinism.
Dermatologic clinics 1988;6(2):217-28.
1988: C Gail Summers; W H Knobloch; C J Witkop; Richard A King
Hermansky-Pudlak syndrome. Ophthalmic findings.
Ophthalmology 1988;95(4):545-54.
1988: Richard A King; D P Olds; D Townsend
Mechanisms of hypopigmentation in human oculocutaneous albinism.
Progress in clinical and biological research 1988;256():183-91.
1986: Richard A King; J D Wirtschafter; D P Olds; J Brumbaugh
Minimal pigment: a new type of oculocutaneous albinism.
Clinical genetics 1986;29(1):42-50.
1985: Richard A King; R A Lewis; D Townsend; A Zelickson; D P Olds; J Brumbaugh
Brown oculocutaneous albinism. Clinical, ophthalmological, and biochemical characterization.
Ophthalmology 1985;92(11):1496-505.
1985: J I Barber; D Townsend; D P Olds; Richard A King
Decreased dopachrome oxidoreductase activity in yellow mice.
The Journal of heredity 1985;76(1):59-60.
1984: J I Barber; D Townsend; D P Olds; Richard A King
Dopachrome oxidoreductase: a new enzyme in the pigment pathway.
The Journal of investigative dermatology 1984;83(2):145-9.