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Comparison of Genome Screens for Two Independent Cohorts Provides Replication of Suggestive Linkage of Bone Mineral Density to 3p21 and 1p36

American journal of human genetics, 2003-01, Vol.72 (1), p.144-155

2003

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Identification and functional analysis of novel human melanocortin-4 receptor variants

Diabetes (New York, N.Y.), 1999-03, Vol.48 (3), p.635-639

1999

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Genetic Variation as a Guide to Drug Development

Science (American Association for the Advancement of Science), 1998-09, Vol.281 (5384), p.1820-1821

1998

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A Genome‐Screen of a Large Twin Cohort Reveals Linkage for Quantitative Ultrasound of the Calcaneus to 2q33–37 and 4q12–21

Journal of bone and mineral research, 2004-02, Vol.19 (2), p.270-277

2004

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TULP1 mutation in two extended Dominican kindreds with autosomal recessive Retinitis pigmentosa

Nature genetics, 1998-02, Vol.18 (2), p.177-179

1998

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Construction of a Yeast Artificial Chromosome Contig Spanning the Spinal Muscular Atrophy Disease Gene Region

Proceedings of the National Academy of Sciences - PNAS, 1993-07, Vol.90 (14), p.6801-6805

1993

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Limatin (LIMAB1), an Actin-Binding LIM Protein, Maps to Mouse Chromosome 19 and Human Chromosome 10q25, a Region Frequently Deleted in Human Cancers

Genomics (San Diego, Calif.), 1997-12, Vol.46 (2), p.291-293

1997

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Refinement of the spinal muscular atrophy locus by genetic and physical mapping

American journal of human genetics, 1995, Vol.56 (1), p.202-209

1995

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Refinement of the Spinal Muscular Atrophy Locus to the Interval between D5S435 and MAP1B

Genomics (San Diego, Calif.), 1993-02, Vol.15 (2), p.365-371

1993

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Autosomal dominant distal spinal muscular atrophy in four generations

Neurology, 1995-04, Vol.45 (4), p.699-712

1995

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Linkage disequilibrium and haplotype analysis among polish families with spinal muscular atrophy

American journal of human genetics, 1995, Vol.56 (1), p.210-215

1995

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Homozygosity and Physical Mapping of the Autosomal Recessive Retinitis Pigmentosa Locus (RP14) on Chromosome 6p21.3

Genomics (San Diego, Calif.), 1998-03, Vol.48 (2), p.171-177

1998

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Assessment of nonallelic genetic heterogeneity of chronic (type II and III) spinal muscular atrophy

Human heredity, 1993-11, Vol.43 (6), p.380-387

1993

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Fine-mapping of the spinal muscular atrophy locus to a region flanked by MAP1B and D5S6

Genomics (San Diego, Calif.), 1992-08, Vol.13 (4), p.991-998

1992

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Spinal muscular atrophy is not the result of mutations at the beta-hexosaminidase or GM2-activator locus

Neurology, 1991-09, Vol.41 (9), p.1418

1991

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Progress Toward Cloning of the Gene Responsible for Childhood Spinal Muscular Atrophy

Seminars in neurology, 1993-09, Vol.13 (3), p.276-282

1993

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Linkage and potential association of obesity-related phenotypes with two genes on chromosome 12q24 in a female dizygous twin cohort

European journal of human genetics : EJHG, 2006-03, Vol.14 (3), p.340-348

2006

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Cumulative life course impairment in psoriasis: patient perception of disease‐related impairment throughout the life course

British journal of dermatology (1951), 2011-05, Vol.164, p.1-14

2011

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Topical treatment of psoriasis: questionnaire results on topical therapy accessibility and influence of body surface area on usage

Journal of the European Academy of Dermatology and Venereology, 2017-07, Vol.31 (7), p.1188-1195

2017

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Clinical Trial and Postmarketing Safety of Onasemnogene Abeparvovec Therapy

Drug safety, 2021-10, Vol.44 (10), p.1109-1119

2021

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Topical treatment of psoriasis: questionnaire results on topical therapy as long-term continuous treatment and use on specific body sites

The Journal of dermatological treatment, 2021-11, Vol.32 (8), p.916-921

2021

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Prevalence and epidemiologic correlates of human T cell lymphotropic virus infection among intravenous drug users

The Journal of infectious diseases, 1994-05, Vol.169 (5), p.962-967

1994

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Enzymatic-ultraviolet method for measuring lactose in milk: collaborative study

Journal of the Association of Official Analytical Chemists, 1984-05, Vol.67 (3), p.637-640

1984

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High-performance liquid chromatographic determination of pyridoxine and congeners in biological fluids of man after high-dose therapy

Journal of chromatography, 1980-01, Vol.183 (4), p.492-498

1980

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Comparison of Genome Screens for Two Independent Cohorts Provides Replication of Suggestive Linkage of Bone Mineral Density to 3p21 and 1p36

Identification and functional analysis of novel human melanocortin-4 receptor variants

Genetic Variation as a Guide to Drug Development

A Genome‐Screen of a Large Twin Cohort Reveals Linkage for Quantitative Ultrasound of the Calcaneus to 2q33–37 and 4q12–21

TULP1 mutation in two extended Dominican kindreds with autosomal recessive Retinitis pigmentosa

Construction of a Yeast Artificial Chromosome Contig Spanning the Spinal Muscular Atrophy Disease Gene Region

Identification and Characterization of the Mouse Obesity Gene tubby: A Member of a Novel Gene Family

Limatin (LIMAB1), an Actin-Binding LIM Protein, Maps to Mouse Chromosome 19 and Human Chromosome 10q25, a Region Frequently Deleted in Human Cancers

Refinement of the spinal muscular atrophy locus by genetic and physical mapping

Refinement of the Spinal Muscular Atrophy Locus to the Interval between D5S435 and MAP1B

Autosomal dominant distal spinal muscular atrophy in four generations

Linkage disequilibrium and haplotype analysis among polish families with spinal muscular atrophy

Homozygosity and Physical Mapping of the Autosomal Recessive Retinitis Pigmentosa Locus (RP14) on Chromosome 6p21.3

Assessment of nonallelic genetic heterogeneity of chronic (type II and III) spinal muscular atrophy

Fine-mapping of the spinal muscular atrophy locus to a region flanked by MAP1B and D5S6

Spinal muscular atrophy is not the result of mutations at the beta-hexosaminidase or GM2-activator locus

Progress Toward Cloning of the Gene Responsible for Childhood Spinal Muscular Atrophy

Linkage and potential association of obesity-related phenotypes with two genes on chromosome 12q24 in a female dizygous twin cohort

Cumulative life course impairment in psoriasis: patient perception of disease‐related impairment throughout the life course

Topical treatment of psoriasis: questionnaire results on topical therapy accessibility and influence of body surface area on usage

Clinical Trial and Postmarketing Safety of Onasemnogene Abeparvovec Therapy

Topical treatment of psoriasis: questionnaire results on topical therapy as long-term continuous treatment and use on specific body sites

Prevalence and epidemiologic correlates of human T cell lymphotropic virus infection among intravenous drug users

Enzymatic-ultraviolet method for measuring lactose in milk: collaborative study

High-performance liquid chromatographic determination of pyridoxine and congeners in biological fluids of man after high-dose therapy

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