R. King

发表

Gene expression profiling of bronchoalveolar lavage cells in acute lung rejection.

M. Hertz, V. Gimino, J. Lande, 2003, American journal of respiratory and critical care medicine.

BRCA 1 Susceptibility Markers and Postmenopausal Breast Cancer : The Iowa Women ’ s Health Study 1

T. Sellers, A. Folsom, S. Rich, 2000 .

Linkage Analysis of a Cluster-Based Quantitative Phenotype Constructed from Pulmonary Function Test Data in 27 Multigenerational Families with Multiple Asthmatic Members

Michael B. Miller, C. Reilly, W. Oetting, 2007, Human Heredity.

Diagnosis of oculocutaneous albinism with molecular analysis.

C. Summers, W. Oetting, R. King, 1996, American journal of ophthalmology.

Spectrum of foveal development in albinism detected with optical coherence tomography.

P. S. Harvey, C. Summers, R. King, 2006, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

Efficacy of spectacles in persons with albinism.

C. Summers, J. Lavoie, R. King, 2004, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

Stereopsis in patients with albinism: clinical correlates.

C. Summers, R. King, K. A. Lee, 2001, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

Etiology of sudden death in the community: results of anatomical, metabolic, and genetic evaluation.

Fred S Apple, Richard King, A. Adabağ, 2010, American heart journal.

A genome-wide search for asthma susceptibility loci in ethnically diverse populations

Farhad Imani, Alan R. Leff, James L. Weber, 1997, Nature Genetics.

New locus for autosomal dominant high myopia maps to the long arm of chromosome 17.

O. Mäkitie, M. Devoto, W. Cole, 2003, Investigative ophthalmology & visual science.

CD14 Promoter Polymorphisms in Atopic Families: Implications for Modulated Allergen-Specific Immunoglobulin E and G1 Responses

W. Oetting, S. Basu, R. King, 2006, International Archives of Allergy and Immunology.

Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brain.

I. Scheffer, D. Ledbetter, C. Walsh, 1997, Human molecular genetics.

The Pigmentary System: Physiology and Pathophysiology: Second Edition

James J. Nordlund, Richard A. King, Vincent J. Hearing, 2007 .

Identification of genes expressed in a human scleral cDNA library.

T. Young, R. King, J. Rada, 2002, Molecular vision.

Alternative splicing of the tyrosinase gene transcript in normal human melanocytes and lymphocytes.

W. Oetting, R. King, M. Brott, 2001, The Journal of investigative dermatology.

The role of heredity in cancer.

C. Bloomfield, R. King, E. Levine, 1989, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

P gene mutations associated with oculocutaneous albinism type II (OCA2)

W. Oetting, R. King, M. Brott, 2005, Human mutation.

Validation study of self-reported measures of fat distribution.

T. Sellers, J. Potter, S. Rich, 1996, International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity.

Hermansky-Pudlak syndrome. Ophthalmic findings.

C. Summers, R. King, W. Knobloch, 1988 .

Folate metabolism and chromosomal stability in the fragile X syndrome.

R. Branda, W. Woods, D. Arthur, 1984, The American journal of medicine.

Albinism and Hermansky‐Pudlak Syndrome

C. Summers, R. King, C. Gail Summers, 2005 .

Chapter 35 – Albinism

R. King, R. King, 1987 .

Abnormalities of the central visual pathways in Prader-Willi syndrome associated with hypopigmentation.

D. Creel, D. Arthur, R. King, 1986, The New England journal of medicine.

Ehlers-Danlos syndrome type VIII.

D. Nelson, R. King, D. Nelson, 1981, Journal of the American Academy of Dermatology.

Autosomal recessively inherited ocular albinism. A new form of ocular albinism affecting females as severely as males.

W. Green, R. King, F. O'Donnell, 1978, Archives of ophthalmology.

Does tyrosinase exist in neuromelanin-pigmented neurons in the human substantia nigra?

S. Ito, R. King, T. Nagatsu, 1998, Neuroscience Letters.

Retroviral-mediated transfer of the iduronate-2-sulfatase gene into lymphocytes for treatment of mild Hunter syndrome (mucopolysaccharidosis type II).

R. Latchaw, R. McIvor, B. Blazar, 1996, Human gene therapy.

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".

R. Sturm, J. Nordlund, V. Hearing, 1996, American journal of human genetics.

A gene causing Hermansky-Pudlak syndrome in a Puerto Rican population maps to chromosome 10q2.

J. White, W. Oetting, R. King, 1995, American journal of human genetics.

INTERACTIONS AMONG RHEUMATOID FACTORS, γG ANTIBODIES, LYMPHOCYTES, AND PHAGOCYTES

R. King, R. Messner, Ralph C. Williams, 1969 .

Human lymphocyte transformation induced by anti-gamma globulin factors.

R. Williams, R. King, R. Messner, 1969, Arthritis and rheumatism.

Genetic Linkage Analysis of Hereditary Arthro-Ophthalmopathy (Stickler Syndrome) and the Type 11 Procollagen Gene

S. Jimenez, J. Uitto, D. Prockop, 2006 .

Tyrosinase gene mutations associated with type IB ("yellow") oculocutaneous albinism.

R. Spritz, L. Giebel, C. Jackson, 1991, American journal of human genetics.

MC1R mutations modify the classic phenotype of oculocutaneous albinism type 2 (OCA2).

C. Summers, W. Oetting, R. King, 2003, American journal of human genetics.

Hypopigmentation in the Prader-Willi syndrome.

J. White, D. Arthur, D. Ball, 1987, American journal of human genetics.

Albinism and Hermansky-Pudlak syndrome in Puerto Rico.

C. Summers, R. King, F. Gaudier, 1990, Boletin de la Asociacion Medica de Puerto Rico.

Analysis of tyrosinase gene mutations using direct automated infrared fluorescence DNA sequencing of amplified exons

C. Summers, L. Middendorf, W. Oetting, 1994, Electrophoresis.

Genetic analysis of mammographic breast density in adult women: evidence of a gene effect.

J. Pankow, D. Grabrick, T. Sellers, 1997, Journal of the National Cancer Institute.

Hereditary mucoepithelial dysplasia: a disease apparently of desmosome and gap junction formation.

J. White, R. King, J. Sauk, 1979, American journal of human genetics.

Pathogenesis of pulmonary fibrosis: platelet-derived growth factor precedes structural alterations in the Hermansky-Pudlak syndrome.

J. White, M. Peterson, P. Bitterman, 1994, The Journal of laboratory and clinical medicine.

Tyrosine uptake in normal and albino hairbulbs

R. King, D. P. Olds, 2004, Archives of Dermatological Research.

A new form of Ehlers-Danlos syndrome. Fibronectin corrects defective platelet function.

R. King, D. Hammerschmidt, L. Furcht, 1980, JAMA.

Electrophoretic pattern of human hairbulb tyrosinase.

R. King, D. P. Olds, R. King, 1981, The Journal of investigative dermatology.

Dopachrome oxidoreductase: a new enzyme in the pigment pathway.

R. King, D. P. Olds, D. Townsend, 1984, The Journal of investigative dermatology.

Combined chemical and electron microscopic studies of pheomelanosomes in human red hair.

S. Ito, K. Jimbow, R. King, 1983, The Journal of investigative dermatology.

Genomewide screen and identification of gene-gene interactions for asthma-susceptibility loci in three U.S. populations: collaborative study on the genetics of asthma.

T. Beaty, C. Ober, K. Barnes, 2001, American journal of human genetics.

Tyrosinase inhibition due to interaction of homocyst(e)ine with copper: the mechanism for reversible hypopigmentation in homocystinuria due to cystathionine beta-synthase deficiency.

R. King, O. Reish, M. Tsai, 1995, American journal of human genetics.

Ophthalmic features of minimal pigment oculocutaneous albinism.

C. Summers, R. King, C. Gail Summers, 1994, Ophthalmology.

The White platelet syndrome: a new autosomal dominant platelet disorderI. Structural abnormalities

G. Vercellotti, N. Key, R. King, 2004, Platelets.

A ‘touch’ of the White platelet syndrome

G. Vercellotti, N. Key, R. King, 2005, Platelets.

Molecular basis of albinism: Mutations and polymorphisms of pigmentation genes associated with albinism

W. Oetting, R. King, R. King, 1999, Human mutation.

Three different frameshift mutations of the tyrosinase gene in type IA oculocutaneous albinism.

J. White, C. Summers, W. Oetting, 1991, American journal of human genetics.

Linkage analysis with multiplexed short tandem repeat polymorphisms using infrared fluorescence and M13 tailed primers.

W S Oetting, R A King, T. Sellers, 1995, Genomics.

Molecular basis of oculocutaneous albinism.

W. Oetting, R. King, R. King, 1994, The Journal of investigative dermatology.

Tyrosinase gene mutations in oculocutaneous albinism 1 (OCA1): definition of the phenotype

C. Summers, W. Oetting, R. King, 2003, Human Genetics.

Bronchoalveolar Lavage Cell Gene Expression in Acute Lung Rejection: Development of a Diagnostic Classifier

M. Hertz, J. Lande, T. Berryman, 2008, Transplantation.

Novel insights into lung transplant rejection by microarray analysis.

M. Hertz, J. Lande, T. Berryman, 2007, Proceedings of the American Thoracic Society.

Hepatitis-associated antigen in atomic bomb survivors and nonexposed control subjects: seroepidemiologic survey in a fixed cohort.

R. King, J. Belsky, T. Ishimaru, 1973, The Journal of infectious diseases.

Hepatitis-associated Antigen in Atomic Bomb Survivors and Nonexposed Control Subjects: Seroepidemiologic Survey in

R. King, J. Belsky, T. Ishimaru, 1973 .

Oculocutaneous albinism type 1: the last 100 years.

W. Oetting, R. King, J. Fryer, 2003, Pigment cell research.

Human Albinism and Mouse Models

W. Oetting, R. King, I. Jackson, 1994 .

A tyrosinase gene missense mutation in temperature-sensitive type I oculocutaneous albinism. A human homologue to the Siamese cat and the Himalayan mouse.

R. Spritz, L. Giebel, R. King, 1991, The Journal of clinical investigation.

Dopa oxidase activity in human hair bulbs measured by high-performance liquid chromatography.

R. King, D. P. Olds, D. Townsend, 1986, The Journal of investigative dermatology.

Hairbulb tyrosinase activity in oculocutaneous albinism

R. King, C. Witkop, CARL J. WITKOP, 1976, Nature.

Microphthalmia-associated transcription factor (MITF) locus lacks linkage to human vitiligo or osteopetrosis: an evaluation.

J. Nordlund, W. Oetting, R. Boissy, 1999, Pigment cell research.

Characterization of human hairbulb tyrosinase: properties of normal and albino enzyme.

R. King, D. P. Olds, C. Witkop, 1978, The Journal of investigative dermatology.

Detection of mutations in the tyrosinase gene in a patient with type IA oculocutaneous albinism.

R. Spritz, L. Giebel, R. King, 1990, The New England journal of medicine.

Hairbulb tyrosinase activity in oculocutaneous albinism: suggestions for pathway control and block location.

R. King, D. P. Olds, 1985, American journal of medical genetics.

Decreased dopachrome oxidoreductase activity in yellow mice.

R. King, D. P. Olds, D. Townsend, 1985, The Journal of heredity.

Purification and characterization of dopachrome tautomerase (DT).

W. Oetting, R. King, D. Townsend, 2008, Pigment cell research.

Temperature-sensitive tyrosinase associated with peripheral pigmentation in oculocutaneous albinism.

J. White, C. Summers, R. Spritz, 1991, The Journal of clinical investigation.

Visual anomalies associated with albinism.

C. Summers, D. Creel, R. King, 1990, Ophthalmic paediatrics and genetics.

Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4.

M. Brilliant, M. Davisson, J. Newton, 2001, American journal of human genetics.

Molecular analysis of type I-A (tyrosinase negative) oculocutaneous albinism

W. Oetting, R. King, R. King, 1992, Human Genetics.

Auditory brainstem anomalies in human albinos.

D. Creel, S. R. Garber, R. King, 1980, Science.

On the analysis of the pathophysiology of Chediak-Higashi syndrome. Defects expressed by cultured melanocytes.

Z. Abdel‐Malek, J. Nordlund, R. Boissy, 1994, Laboratory investigation; a journal of technical methods and pathology.

Posterior staphyloma in oculocutaneous albinism: another possible cause of reduced visual acuity.

C. Summers, M. Brilliant, Jennifer L. Anderson, 2015, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

Variable expression of vision in sibs with albinism.

C. Summers, D. Creel, R. King, 1991, American journal of medical genetics.

Minimal pigment: a new type of oculocutaneous albinism

R. King, J. Brumbaugh, D. P. Olds, 1986, Clinical genetics.

Brown Ocuuiocutaneous Albinism: Clinical, Ophthalmological, and Biochemical Characterization

R. Lewis, R. King, J. Brumbaugh, 1985 .

Oculocutaneous albinoidism as a manifestation of reduced neural crest derivatives in the Prader-Willi syndrome.

D. Ledbetter, R. Borda, R. Ferrell, 1982, American journal of ophthalmology.

Human Albinism and Animal Models of Albinism

R. King, C. Witkop, D. Townsend, 1988 .

Analysis of tyrosinase mutations associated with tyrosinase-related oculocutaneous albinism (OCA1).

W. Oetting, R. King, R. King, 1994, Pigment cell research.

Molecular basis of type I (tryrosinase‐related) oculocutaneous albinism: Mutations and polymorphisms of the human tyrosinase gene

W. Oetting, R. King, R. King, 1993 .

African origin of an intragenic deletion of the human P gene in tyrosinase positive oculocutaneous albinism

M. Brilliant, U. Francke, Y. Nakatsu, 1994, Nature Genetics.

Brown oculocutaneous albinism. Clinical, ophthalmological, and biochemical characterization.

R. Lewis, R. King, J. Brumbaugh, 1985, Ophthalmology (Rochester, Minn.).

Identification and characterization of a DNase hypersensitive region of the human tyrosinase gene.

W. Oetting, R. King, J. Fryer, 2003, Pigment cell research.

Evidence for locus heterogeneity in Puerto Ricans with Hermansky-Pudlak syndrome.

J. White, M. Kaiser-Kupfer, W. Gahl, 1997, American journal of human genetics.

The Mouse Pink-Eyed Dilution Gene: Association with Human Prader-Willi and Angelman Syndromes

M. Lyon, M. Brilliant, Y. Gondo, 1992, Science.

Hypopigmentation in Angelman syndrome.

J. White, R. King, G. Wiesner, 1993, American journal of medical genetics.

Molecular analysis of an extended family with type IA (tyrosinase-negative) oculocutaneous albinism.

J. White, A. Paller, W. Oetting, 1991, The Journal of investigative dermatology.

Segregation analysis of brown oculocutaneous albinism

R. King, S. Rich, 1986, Clinical genetics.

Detection of heterozygotes for tyrosinase-negative oculocutaneous albinism by hairbulb tyrosinase assay.

R. King, C. Witkop, R. King, 1977, American journal of human genetics.

A frequent tyrosinase gene mutation in classic, tyrosinase-negative (type IA) oculocutaneous albinism.

R. Spritz, L. Giebel, R. King, 1990, Proceedings of the National Academy of Sciences of the United States of America.

Functional genomics tools for the analysis of zebrafish pigment.

S. Sivasubbu, S. Ekker, R. King, 2004, Pigment cell research.

Non-random distribution of missense mutations within the human tyrosinase gene in type I (tyrosinase-related) oculocutaneous albinism.

W. Oetting, R. King, M. Mentink, 1991, Molecular biology & medicine.

Genetic Hypomelanoses: Generalized Hypopigmentation

P. Bahadoran, J. Ortonne, J. Nordlund, 2007 .

Chapter 5. Albinism: Ocular and Oculocutaneous Albinism and Hermansky-Pudlak Syndrome

C. Summers, R. King, R. King, 2010 .

Change in visual acuity in albinism in the early school years.

C. Summers, R. King, A. Holleschau, 2012, Journal of pediatric ophthalmology and strabismus.

Type 2 oculocutaneous albinism (OCA2) in Zimbabwe and Cameroon: distribution of the 2.7-kb deletion allele of the P gene

M. Brilliant, R. King, P. Lund, 1997, Human Genetics.

The mouse pink-eyed dilution gene: association with hypopigmentation in Prader-Willi and Angelman syndromes and with human OCA2.

T. Meitinger, S. Schuffenhauer, M. Brilliant, 1994, Pigment cell research.

Chromosome breaks and sister chromatid exchanges in albinos in Nigeria

J. Červenka, R. King, C. Witkop, 1979, Clinical genetics.

Asymmetric visually evoked potentials in human albinos: evidence for visual system anomalies.

D. Creel, R. King, C. Witkop, 1974, Investigative ophthalmology.

Hermansky-Pudlak syndrome (HPS): a proposed block in glutathione peroxidase.

J. White, R. King, C. Witkop, 1973, Oral surgery, oral medicine, and oral pathology.

Positive angle kappa in albinism.

C. Summers, J. Lavoie, R. King, 2004, American journal of ophthalmology.

Oculocutaneous albinism: variable expressivity of nystagmus in a sibship.

J. Bateman, R. King, P. Cheong, 1992, Journal of pediatric ophthalmology and strabismus.

Albinism in Nigeria with delineation of new recessive oculocutaneous type

D. Creel, R. King, C. Witkop, 1980, Clinical genetics.

Molecular basis of type IA (tyrosinase negative) oculocutaneous albinism.

W. Oetting, R. King, R. King, 2008, Pigment cell research.

The mouse pale ear (ep) mutation is the homologue of human Hermansky-Pudlak syndrome.

M. Brilliant, M. Bayer, R. King, 1997, Proceedings of the National Academy of Sciences of the United States of America.

A dinucleotide deletion (-delta GA115) in the tyrosinase gene responsible for type I-A (tyrosinase negative) oculocutaneous albinism in a Pakistani individual.

W. Oetting, R. King, J. Fryer, 1993, Human molecular genetics.

A frequent tyrosinase gene mutation associated with type I-A (tyrosinase-negative) oculocutaneous albinism in Puerto Rico.

W. Oetting, S. A. Brown, R. King, 1993, American journal of human genetics.

Analysis of mutations in the copper B binding region associated with type I (tyrosinase-related) oculocutaneous albinism.

W. Oetting, R. King, 1992, Pigment cell research.

PCR detection of a TaqI polymorphism at the CCAATT box of the human tyrosinase (TYR) gene.

W. Oetting, R. King, M. Mentink, 1991, Nucleic acids research.

Mutations of the human P gene associated with Type II oculocutaneous albinism (OCA2). Mutations in brief no. 205. Online.

M. Brilliant, W. Oetting, R. King, 1998, Human mutation.

Estimation of carrier frequency of a 2.7 kb deletion allele of the P gene associated with OCA2 in African‐Americans

M. Brilliant, R. King, S. Laken, 1996 .

Positive angle kappa in albinism.

C. Summers, J. Lavoie, R. King, 2004, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

Evolution of the tyrosinase related gene (TYRL) in primates.

W. Oetting, R. King, D. Townsend, 1993, Pigment cell research.

The clinical spectrum of albinism in humans.

M. Brilliant, W. Oetting, R. King, 1996, Molecular medicine today.

LINKAGE ANALYSIS IN X-LINKED OCULAR ALBINISM

J. Graham, R. King, B. Demartinville, 1987, Pediatric Research.

Albinism and the associated ocular defects.

C. Summers, W. Oetting, R. King, 1994, Metabolic, pediatric, and systemic ophthalmology.

Grating acuity in albinism in the first three years of life.

C. Summers, R. King, Sarah J. Whang, 2002, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

Lymphocyte reactivity in rheumatoid arthritis. Mixed lymphocyte culture.

R. King, E. Caperton, D. Baker, 1975, Annals of the rheumatic diseases.

Congenital adrenal hypoplasia and selective absence of pituitary luteinizing hormone: a new autosomal recessive syndrome.

B. Scheithauer, U. Francke, B. Burke, 1988, American journal of medical genetics.

Genome screening in human systemic lupus erythematosus: results from a second Minnesota cohort and combined analyses of 187 sib-pair families.

P. Gaffney, S. Rich, T. Behrens, 2000, American journal of human genetics.

A genome-wide search for susceptibility genes in human systemic lupus erythematosus sib-pair families.

P. Gaffney, S. Rich, T. Behrens, 1998, Proceedings of the National Academy of Sciences of the United States of America.

Visualizing human leukocyte antigen class II risk haplotypes in human systemic lupus erythematosus.

James T. Elder, P. Gregersen, P. Gaffney, 2002, American journal of human genetics.

The genetic basis of common diseases.

Richard A. King, Jerome I. Rotter, Arno G. Motulsky, 2002 .

Duplication of 7p: further delineation of the phenotype and restriction of the critical region to the distal part of the short arm.

G. Dewald, R. King, O. Reish, 1996, American journal of medical genetics.

Thromboxane Responsiveness of Dog Platelets Is Inherited as an Autosomal Recessive Trait

R. King, G. Johnson, L. Leis, 1991, Thrombosis and Haemostasis.

Genetic linkage analysis of hereditary arthro-ophthalmopathy (Stickler syndrome) and the type II procollagen gene.

S. Jimenez, J. Uitto, D. Prockop, 1989, American journal of human genetics.

A 122.5-kilobase deletion of the P gene underlies the high prevalence of oculocutaneous albinism type 2 in the Navajo population.

M. Hammer, M. Brilliant, R. Erickson, 2003, American journal of human genetics.

Inclusion of risk factor covariates in a segregation analysis of a population‐based sample of 426 breast cancer families

D. Grabrick, T. Sellers, V. Anderson, 1999, Genetic epidemiology.

Molecular genetic differentiation in earthworms inhabiting a heterogeneous Pb-polluted landscape.

M. Hodson, S. Stürzenbaum, P. Kille, 2010, Environmental pollution.

Duplication of 7p: Further delineation of the phenotype and restriction of the critical region to the distal part of the short arm

G. Dewald, R. King, O. Reish, 1996 .

Clinical, histologic, cytologic, and ultrastructural characteristics of the oral lesions from hereditary mucoepithelial dysplasia. A disease of gap junction and desmosome formation.

J. White, R. King, J. Sauk, 1978, Oral surgery, oral medicine, and oral pathology.

Identification of carriers of Duchenne muscular dystrophy: value of molecular analysis.

S. Rich, C. Boehm, R. King, 1988, American journal of medical genetics.

Fifty-year follow-up of cancer incidence in a historical cohort of Minnesota breast cancer families.

T M Therneau, W S Oetting, R A King, 1999, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

The R402Q tyrosinase variant does not cause autosomal recessive ocular albinism

C. Summers, W. Oetting, R. King, 2009, American journal of medical genetics. Part A.

Management of Genetic Syndromes: Third Edition

C. Summers, R. King, 2010 .

BRCA1 susceptibility markers and postmenopausal breast cancer: the Iowa Women's Health Study.

T. Sellers, A. Folsom, S. Rich, 2000, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

Genetic anticipation and breast cancer: a prospective follow‐up study

A. Paterson, T. Sellers, Jian Huang, 1999, Breast Cancer Research and Treatment.

A genome-wide search for quantitative trait loci contributing to variation in seasonal pollen reactivity.

T. Beaty, E. Bleecker, C. Ober, 2006, The Journal of allergy and clinical immunology.

A genome-wide search for allergic response (atopy) genes in three ethnic groups: Collaborative Study on the Genetics of Asthma

T. Beaty, E. Bleecker, E. Lange, 2003, Human Genetics.

Familial male breast cancer.

R. King, I. Lerner, A. Hauser, 1992, American journal of medical genetics.

Determination of lymphocyte immunophenotypic values for normal full-term cord blood.

M. Meyer, R. King, G. Naus, 1996, American journal of clinical pathology.

A second locus for familial high myopia maps to chromosome 12q.

W S Oetting, R A King, L. Atwood, 1998, American journal of human genetics.

Identification of a novel transcript produced by the gene responsible for the Hermansky-Pudlak syndrome in Puerto Rico.

M. Brilliant, W. Oetting, R. King, 1998, The Journal of investigative dermatology.

X-linked high myopia associated with cone dysfunction.

T. Rosenberg, A. Motulsky, L. Atwood, 2004, Archives of ophthalmology.

Evidence that a locus for familial high myopia maps to chromosome 18p.

L. Atwood, W. Oetting, T. Young, 1998, American journal of human genetics.

Persistence of hepatitis associated antigen within a fixed population.

R. King, M. Yamakido, J. Belsky, 1972, Archives of environmental health.

Genetic linkage and transmission disequilibrium of marker haplotypes at chromosome 1q41 in human systemic lupus erythematosus

James T. Elder, P. Gaffney, S. Gabriel, 2001, Arthritis research.

The Prevalence of Attention-Deficit/ Hyperactivity Disorder Among Persons With Albinism

C. Summers, R. King, A. Holleschau, 2007, Journal of child neurology.

Oculocutaneous albinism in an isolated Tonga community in Zimbabwe.

M. Brilliant, R. King, P. Lund, 1997, Journal of medical genetics.

Tonga community in Zimbabwe . Oculocutaneous albinism in an isolated

M. Brilliant, R. King, P. Lund, 2004 .

Albinism in England.

R. King, C. Witkop, B. Jay, 1982, Birth defects original article series.

Minimum guidelines for the delivery of clinical genetics services. The Evaluation of Clinical Services Subcommittee, Great Lakes Regional Genetics Group.

R. Laxová, D. Weaver, R. King, 1993, American Journal of Human Genetics.

Preliminary sibpair linkage analysis of percent mammographic density.

T. Sellers, C. Vachon, C. Kuni, 1999, Journal of the National Cancer Institute.

Segregation analysis of breast cancer: A comparison of type‐dependent age‐at‐onset versus type‐dependent susceptibility models

T. Sellers, C. Vachon, V. Anderson, 1996, Genetic epidemiology.

Editor's comments

R. King, 2001, Genetics in Medicine.

Epidemiologic and genetic follo‐up study of 544 Minnesota breast cancer families: Design and methods

T. Sellers, J. Potter, V. Anderson, 1995, Genetic epidemiology.

Estimation of carrier frequency of a 2.7 kb deletion allele of the P gene associated with OCA2 in African-Americans.

M. Brilliant, R. King, S. Laken, 1996, Human mutation.

Correlation of grating acuity with letter recognition acuity in children with albinism.

C. Summers, R. King, A. Holleschau, 2006, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.