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1. A homozygous missense variant in type I keratin KRT25 causes autosomal recessive woolly hair. Issue 10 (9th July 2015)

2. Associations Between Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Variants and Risk of Coronavirus Disease 2019 (COVID-19) Hospitalization Among Confirmed Cases in Washington State: A Retrospective Cohort Study . (12th April 2022)

3. Benchmarking association analyses of continuous exposures with RNA-seq in observational studies. Issue 6 (20th May 2021)

4. Clinical, biochemical and genetic characteristics of MOGS-CDG: a rare congenital disorder of glycosylation. Issue 11 (5th July 2022)

5. FAM92A Underlies Nonsyndromic Postaxial Polydactyly in Humans and an Abnormal Limb and Digit Skeletal Phenotype in Mice. (5th November 2018)

6. Functional divergence of the two Elongator subcomplexes during neurodevelopment. Issue 7 (13th June 2022)

7. Genetic architectures of proximal and distal colorectal cancer are partly distinct. Issue 7 (25th February 2021)

8. Incidence of Medically Attended Acute Respiratory Illnesses Due to Respiratory Viruses Across the Life Course During the 2018/19 Influenza Season. (16th February 2021)

9. Influence of common and rare genetic variation on warfarin dose among African–Americans and European–Americans using the exome array. (July 2017)

10. Lung Function in African American Children with Asthma Is Associated with Novel Regulatory Variants of the KIT Ligand KITLG/SCF and Gene-By-Air-Pollution Interaction. Issue 3 (1st July 2020)