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51

Officers, Committees and Representatives of the American Dairy Science Association, July 1988–1989

McWilliam, Peter, Farrar, G.Jane, Kenna, Paul, Bradley, Daniel G., Humphries, Marian M., Sharp, Elizabeth M., McConnell, David J., Lawler, Mark, Sheils, Denise, Ryan, Carmel, Stevens, Karen, Daiger, S

Journal:

Journal of Dairy Science

Year:

1988

Language:

english

File:

PDF, 593 KB

english, 1988

52

Autosomal dominant retinitis pigmentosa (ADRP): Localization of an ADRP gene to the long arm of chromosome 3

McWilliam, Peter, Farrar, G.Jane, Kenna, Paul, Bradley, Daniel G., Humphries, Marian M., Sharp, Elizabeth M., McConnell, David J., Lawler, Mark, Sheils, Denise, Ryan, Carmel, Stevens, Karen, Daiger, S

Journal:

Year:

1989

Language:

english

File:

PDF, 392 KB

english, 1989

53

Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8

Blanton, Susan Halloran, Heckenlively, John R., Cottingham, Anne W., Friedman, Jackie, Sadler, Lori A., Wagner, Michael, Friedman, Lorraine H., Daiger, Stephen P.

Journal:

Year:

1991

Language:

english

File:

PDF, 1.38 MB

english, 1991

54

Human chromosome 8 linkage map based on short tandem repeat polymorphisms: Effect of genotyping errors

Tomfohrde, James, Wood, Stephen, Schertzer, Michael, Wagner, Michael J., Wells, Dan E., Parrish, Julia, Sadler, Lori A., Blanton, Susan H., Daiger, Stephen P., Wang, Zhenyuan, Wilkie, Patricia J., Web

Journal:

Year:

1992

Language:

english

File:

PDF, 835 KB

english, 1992

55

Further evidence of exclusion of linkage between type II autosomal dominant retinitis pigmentosa (ADRP) and D3S47 on 3q

Blanton, S.H., Cottingham, A.W., Giesenschlag, N., Heckenlively, J.R., Humphries, P., Daiger, S.P.

Journal:

Year:

1990

Language:

english

File:

PDF, 284 KB

english, 1990

56

POLYMORPHIC DNA HAPLOTYPES AT THE PHENYLALANINE HYDROXYLASE LOCUS IN PRENATAL DIAGNOSIS OF PHENYLKETONURIA

Daiger, StephenP., Chakraborty, Ranajit, Güttler, Flemming, Lidsky, AlanS., Koch, Richard, Woo, SavioL.C.

Journal:

Year:

1986

Language:

english

File:

PDF, 465 KB

english, 1986

57

Localization of two genes for usher syndrome type I to chromosome 11

Smith, Richard J.H., Lee, Elizabeth C., Kimberling, William J., Daiger, Stephen P., Pelias, Mary Z., Keats, Bronya J.B., Jay, Marcelle, Bird, Alan, Reardon, William, Guest, Mary

Journal:

Year:

1992

Language:

english

File:

PDF, 775 KB

english, 1992

58

Assignment of autosomal dominant spinocerebellar ataxia centromeric to HLA using multilocus linkage analysis

Zoghbi, H.Y., Sandkuyl, L.A., Ott, J., Daiger, S.P., Pollack, M.S., O'Brien, W.E., Beaudet, A.L.

Journal:

Human Immunology

Year:

1988

Language:

english

File:

PDF, 76 KB

english, 1988

59

Multilocus linkage analysis with the human argininosuccinate synthetase gene

Northrup, Hope, Lathrop, Mark, Lu, Shu-Ying, Daiger, Stephen P., Beaudet, Arthur L., O'Brien, William E.

Journal:

Year:

1989

Language:

english

File:

PDF, 320 KB

english, 1989

60

Group-Specific Component (Gc) Proteins Bind Vitamin D and 25-hydroxyvitamin D

Stephen P. Daiger, Mel S. Schanfield and L. L. Cavalli-Sforza

Journal:

Proceedings of the National Academy of Sciences

Year:

1975

Language:

english

File:

PDF, 1.20 MB

english, 1975

61

Visual phenotype in patients with Arg41Gln and Ala196+1bp mutations in the CRX gene

Tzekov, Radouil T., Sohocki, Melanie M., Daiger, Stephen P., Birch, David G.

Journal:

Ophthalmic Genetics

Year:

2000

Language:

english

File:

PDF, 321 KB

english, 2000

62

Evidence for a Novel X-Linked Modifier Locus for Leber Hereditary Optic Neuropathy

Shankar, Suma P., Fingert, John H., Carelli, Valerio, Valentino, Maria L., King, Terri M., Daiger, Stephen P., Salomao, Solange R., Berezovsky, Adriana, Belfort, Rubens, Braun, Terri A., Sheffield, Va

Journal:

Ophthalmic Genetics

Year:

2008

Language:

english

File:

PDF, 5.84 MB

english, 2008

63

Mutations in the X-Linked Retinitis Pigmentosa Genes RPGR and RP2 Found in 8.5% of Families with a Provisional Diagnosis of Autosomal Dominant Retinitis Pigmentosa

Churchill, Jennifer D., Bowne, Sara J., Sullivan, Lori S., Lewis, Richard Alan, Wheaton, Dianna K., Birch, David G., Branham, Kari E., Heckenlively, John R., Daiger, Stephen P.

Journal:

Investigative Ophthalmology & Visual Science

Year:

2013

Language:

english

File:

PDF, 369 KB

english, 2013

64

PITPNM3 is an uncommon cause of cone and cone-rod dystrophies

Köhn, Linda, Kohl, Susanne, Bowne, Sara J, Sullivan, Lori S, Kellner, Ulrich, Daiger, Stephen P, Sandgren, Ola, Golovleva, Irina

Journal:

Ophthalmic Genetics

Year:

2010

Language:

english

File:

PDF, 527 KB

english, 2010

65

Exclusion of the human collagen type XVII (COL17A1) gene as the cause of Thiel-Behnke corneal dystrophy (CDB2) on chromosome 10q23-q25

Sullivan, Lori S., Zhao, Xinping, Bowne, Sara J., Xu, Xiangyang, Daiger, Stephen P., Yee, Steven B., Yee, Richard W.

Journal:

Current Eye Research

Year:

2003

Language:

english

File:

PDF, 64 KB

english, 2003

66

Comprehensive Registration of DNA Sequence Variants Associated with Inherited Retinal Diseases in Leiden Open Variation Databases

Cremers, Frans P.M., den Dunnen, Johan T., Ajmal, Muhammad, Hussain, Alamdar, Preising, Markus N., Daiger, Stephen P., Qamar, Raheel

Journal:

Year:

2014

Language:

english

File:

PDF, 110 KB

english, 2014

67

The Measurement of Specific Resistance by Eddy Current Shielding

Kouwenhoven, W. B., Daiger, G. P.

Journal:

Review of Scientific Instruments

Year:

1934

Language:

english

File:

PDF, 714 KB

english, 1934

68

Genes and Mutations Causing Autosomal Dominant Retinitis Pigmentosa

Daiger, S. P., Bowne, S. J., Sullivan, L. S.

Journal:

Cold Spring Harbor Perspectives in Medicine

Year:

2014

Language:

english

File:

PDF, 528 KB

english, 2014

69

Dinucleotide repeat polymorphism at the CRH gene

Gu, Jessie, Sadler, Lori, Daiger, Stephen, Wells, Dan, Wagner, Michael

Journal:

Human Molecular Genetics

Year:

1993

Language:

english

File:

PDF, 84 KB

english, 1993

70

IMP Dehydrogenase Type 1 Associates with Polyribosomes Translating Rhodopsin mRNA

Mortimer, S. E., Xu, D., McGrew, D., Hamaguchi, N., Lim, H. C., Bowne, S. J., Daiger, S. P., Hedstrom, L.

Journal:

Journal of Biological Chemistry

Year:

2008

Language:

english

File:

PDF, 1.00 MB

english, 2008

71

Defining the Human Macula Transcriptome and Candidate Retinal Disease Genes Using EyeSAGE

Bowes Rickman, Catherine, Ebright, Jessica N., Zavodni, Zachary J., Yu, Ling, Wang, Tianyuan, Daiger, Stephen P., Wistow, Graeme, Boon, Kathy, Hauser, Michael A.

Journal:

Investigative Ophthalmology & Visual Science

Year:

2006

Language:

english

File:

PDF, 342 KB

english, 2006

72

High-Throughput Retina-Array for Screening 93 Genes Involved in Inherited Retinal Dystrophy

Song, Jin, Smaoui, Nizar, Ayyagari, Radha, Stiles, David, Benhamed, Sonia, MacDonald, Ian M., Daiger, Stephen P., Tumminia, Santa J., Hejtmancik, Fielding, Wang, Xinjing

Journal:

Investigative Ophthalmology & Visual Science

Year:

2011

Language:

english

File:

PDF, 669 KB

english, 2011

73

Late-Onset Autosomal Dominant Macular Dystrophy with Choroidal Neovascularization and Nonexudative Maculopathy Associated with Mutation in the RDS Gene

Khani, Shahrokh C., Karoukis, Athanasios J., Young, Joyce E., Ambasudhan, Rajesh, Burch, Tracy, Stockton, Richard, Lewis, Richard Alan, Sullivan, Lori S., Daiger, Stephen P., Reichel, Elias, Ayyagari,

Journal:

Investigative Ophthalmology & Visual Science

Year:

2003

Language:

english

File:

PDF, 499 KB

english, 2003

74

Prevalence of Mutations in eyeGENE Probands With a Diagnosis of Autosomal Dominant Retinitis Pigmentosa

Sullivan, Lori S., Bowne, Sara J., Reeves, Melissa J., Blain, Delphine, Goetz, Kerry, NDifor, Vida, Vitez, Sally, Wang, Xinjing, Tumminia, Santa J., Daiger, Stephen P.

Journal:

Investigative Opthalmology & Visual Science

Year:

2013

Language:

english

File:

PDF, 313 KB

english, 2013

75

Essential and Synergistic Roles of RP1 and RP1L1 in Rod Photoreceptor Axoneme and Retinitis Pigmentosa

Yamashita, T., Liu, J., Gao, J., LeNoue, S., Wang, C., Kaminoh, J., Bowne, S. J., Sullivan, L. S., Daiger, S. P., Zhang, K., Fitzgerald, M. E. C., Kefalov, V. J., Zuo, J.

Journal:

Journal of Neuroscience

Year:

2009

Language:

english

File:

PDF, 2.75 MB

english, 2009

76

Perspective on Genes and Mutations Causing Retinitis Pigmentosa

Daiger, Stephen P.

Journal:

Archives of Ophthalmology

Year:

2007

Language:

english

File:

PDF, 146 KB

english, 2007

77

Founder Effect of a c.828+3A>T Splice Site Mutation in Peripherin 2 ( PRPH2 ) Causing Autosomal Dominant Retinal Dystrophies

Shankar, Suma P., Birch, David G., Ruiz, Richard S., Hughbanks-Wheaton, Dianna K., Sullivan, Lori S., Bowne, Sara J., Stone, Edwin M., Daiger, Stephen P.

Journal:

JAMA Ophthalmology

Year:

2015

Language:

english

File:

PDF, 328 KB

english, 2015

78

Mapping the RP10 locus for autosomal dominant retinitis pigmentosa on 7q: refined genetic positioning and localization within a well-defined YAC contig.

McGuire, R E, Jordan, S A, Braden, V V, Bouffard, G G, Humphries, P, Green, E D, Daiger, S P

Journal:

Genome Research

Year:

1996

Language:

english

File:

PDF, 1.15 MB

english, 1996

79

Molecular analysis of the human vitamin D binding protein (group specific component, Gc) in tuberous sclerosis complex (TSC).

Rodriguez, J A, Evans, R L, Daiger, S P, Northrup, H

Journal:

Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 559 KB

english, 1997

80

Dinuclotide repeat polymorphism at the human tissue plasminogen activator gene (PLAT)

Sadler, L. A., Blanton, S. H., Daiger, S. P.

Journal:

Nucleic Acids Research

Year:

1991

Language:

english

File:

PDF, 1.54 MB

english, 1991

81

Progressive photoreceptor degeneration, outer segment dysplasia, and rhodopsin mislocalization in mice with targeted disruption of the retinitis pigmentosa-1 (Rp1) gene

Gao, J., Cheon, K., Nusinowitz, S., Liu, Q., Bei, D., Atkins, K., Azimi, A., Daiger, S. P., Farber, D. B., Heckenlively, J. R., Pierce, E. A., Sullivan, L. S., Zuo, J.

Journal:

Proceedings of the National Academy of Sciences

Year:

2002

Language:

english

File:

PDF, 831 KB

english, 2002

82

A tight linkage cluster, with two new RFLPs (D8S96 and D8S108), in the interval 8cen-q13

Cottingham, A.W., Sadler, L.A., BIanton, S.H., Wagner, M.J, Weils, D.E., Heckenlively, J.R., Daiger, S.P.

Journal:

Nucleic Acids Research

Year:

1992

Language:

english

File:

PDF, 1.66 MB

english, 1992

83

Inactivation of VCP/ter94 Suppresses Retinal Pathology Caused by Misfolded Rhodopsin in Drosophila

Griciuc, Ana, Aron, Liviu, Roux, Michel J., Klein, Rüdiger, Giangrande, Angela, Ueffing, Marius, Daiger, Stephen P.

Journal:

Year:

2010

Language:

english

File:

PDF, 6.80 MB

english, 2010

84

Tetranucleotide repeat polymorphism (D8S582) for human EST00680 (D8S340E)

Sullivan, L.S., Parrish, J., Wagner, M.J., Wells, D., Blanton, S.H., Daiger, S.P.

Journal:

Human Molecular Genetics

Year:

1994

Language:

english

File:

PDF, 106 KB

english, 1994

85

PCR detection of the BgIII RFLP at the RBP3 locus

Rodriguez, Joseph A., Liou, Greg I., Daiger, Stephen P.

Journal:

Nucleic Acids Research

Year:

1990

Language:

english

File:

PDF, 1.48 MB

english, 1990

86

Correlation of phenotype with genotype in inherited retinal degeneration

Daiger, Stephen P., Sullivan, Lori S., Rodriguez, Joseph A.

Journal:

Behavioral and Brain Sciences

Year:

1995

Language:

english

File:

PDF, 27.04 MB

english, 1995

87

Genetic and functional complexity of inherited retinal degeneration

Daiger, Stephen P., Sullivan, Lori S., Rodriguez, Joseph A.

Journal:

Behavioral and Brain Sciences

Year:

1995

Language:

english

File:

PDF, 27.04 MB

english, 1995

88

A new Sty l RFLP and haplotypes with the Hin dIII RFLP at the D8S5 (TL11) locus

Cottingham, A.W., Blanton, S.H., Retief, A.E., Warnich, L., Daiger, S.P.

Journal:

Nucleic Acids Research

Year:

1991

Language:

english

File:

PDF, 1.82 MB

english, 1991

89

Group-specific component (Gc) proteins bind vitamin D and 25-hydroxyvitamin D.

Daiger, S. P., Schanfield, M. S., Cavalli-Sforza, L. L.

Journal:

Proceedings of the National Academy of Sciences

Year:

1975

Language:

english

File:

PDF, 1.31 MB

english, 1975

90

Diagnosis of a mild peroxisomal phenotype with next-generation sequencing

Ventura, Meredith J., Wheaton, Dianna, Xu, Mingchu, Birch, David, Bowne, Sara J., Sullivan, Lori S., Daiger, Stephen P., Whitney, Annette E., Jones, Richard O., Moser, Ann B., Chen, Rui, Wangler, Mich

Journal:

Molecular Genetics and Metabolism Reports

Year:

2016

Language:

english

File:

PDF, 774 KB

english, 2016

91

NIH Public Access

Sohocki, Melanie M, Daiger, Stephen P, Bowne, Sara J, Rodriquez, Joseph A, Heckenlively, John R, Birch, David G, Mintz-hittner, Helen, Ruiz, Richard S, Lewis, Richard A, Saperstein, David A, Sullivan,

Year:

2008

Language:

english

File:

PDF, 65 KB

english, 2008

92

SeqCNV: a novel method for identification of copy number variations in targeted next-generation sequencing data

Chen, Yong, Zhao, Li, Wang, Yi, Cao, Ming, Gelowani, Violet, Xu, Mingchu, Agrawal, Smriti A., Li, Yumei, Daiger, Stephen P., Gibbs, Richard, Wang, Fei, Chen, Rui

Journal:

BMC Bioinformatics

Year:

2017

Language:

english

File:

PDF, 1.12 MB

english, 2017

93

The Triple Salt Sr 14 [Ta 4 N 13 ][TaN 4 ]O–A Nitridotantalate Oxide with 19-fold Rock Salt Superstructure

Wörsching, Matthias, Daiger, Martin, Hoch, Constantin

Journal:

Inorganic Chemistry

Year:

2017

Language:

english

File:

PDF, 3.99 MB

english, 2017

94

Molecular findings from 537 individuals with inherited retinal disease

Ellingford, Jamie M, Barton, Stephanie, Bhaskar, Sanjeev, O'Sullivan, James, Williams, Simon G, Lamb, Janine A, Panda, Binay, Sergouniotis, Panagiotis I, Gillespie, Rachel L, Daiger, Stephen P, Hall,

Journal:

Journal of Medical Genetics

Year:

2016

Language:

english

File:

PDF, 1016 KB

english, 2016

95

Innovating patient care delivery: DSRIP's interrupted time series analysis paradigm

Shenoy, Amrita G., Begley, Charles E., Revere, Lee, Linder, Stephen H., Daiger, Stephen P.

Journal:

Healthcare (Elsevier)

Year:

2017

Language:

english

File:

PDF, 176 KB

english, 2017

96

Delivery system innovation and collaboration: A case study on influencers of preventable hospitalizations

Shenoy, Amrita, Begley, Charles, Revere, Lee, Linder, Stephen, Daiger, Stephen P.

Journal:

International Journal of Healthcare Management

Year:

2017

Language:

english

File:

PDF, 1.01 MB

english, 2017

97

De Novo Occurrence of a Variant in ARL3 and Apparent Autosomal Dominant Transmission of Retinitis Pigmentosa

Strom, Samuel P., Clark, Michael J., Martinez, Ariadna, Garcia, Sarah, Abelazeem, Amira A., Matynia, Anna, Parikh, Sachin, Sullivan, Lori S., Bowne, Sara J., Daiger, Stephen P., Gorin, Michael B., Sha

Journal:

Year:

2016

Language:

english

File:

PDF, 405 KB

english, 2016

98

Exclusion of Usher syndrome gene from much of chromosome 4

Smith, R.J.H., Holcomb, J.D., Daiger, S.P., Caskey, C.T., Pelias, M.Z., Alford, B.R., Fontenot, D.D., Hejtmancik, J.F.

Journal:

Cytogenetic and Genome Research

Year:

1989

Language:

english

File:

PDF, 1.00 MB

english, 1989

99

Linkage analysis of human chromosome 4: exclusion of autosomal dominant retinitis pigmentosa (ADRP) and detection of new linkage groups

Daiger, S.P., Humphries, M.M., Giesenschlag, N., Sharp, E., McWilliam, P., Farrer, J., Bradley, D., Kenna, P., McConnell, D.J., Sparkes, R.S., Spence, M.A., Heckenlively, J.R., Humphries, P.

Journal:

Cytogenetic and Genome Research

Year:

1989

Language:

english

File:

PDF, 1.49 MB

english, 1989

100

Molecular Defects of the Disease-Causing Human Arrestin-1 C147F Mutant

Vishnivetskiy, Sergey A., Sullivan, Lori S., Bowne, Sara J., Daiger, Stephen P., Gurevich, Eugenia V., Gurevich, Vsevolod V.

Journal:

Investigative Opthalmology & Visual Science

Year:

2018

Language:

english

File:

PDF, 956 KB

english, 2018

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