S. Rasmussen

发表

Somatic mosaicism in a patient with neurofibromatosis type 1.

C. R. Abernathy, S. Colman, M. Wallace, 1996, American journal of human genetics.

Constitutional and mosaic large NF1 gene deletions in neurofibromatosis type 1.

C. Schwartz, S. Colman, M. Wallace, 1998, Journal of medical genetics.

Chromosome 17 loss‐of‐heterozygosity studies in benign and malignant tumors in neurofibromatosis type 1

S. Colman, K. Roux, M. Wallace, 2000, Genes, chromosomes & cancer.

Genetic disease in offspring of long-term survivors of childhood and adolescent cancer.

L. Strong, R. Connelly, J. Mulvihill, 1998, American journal of human genetics.

Gliomas presenting after age 10 in individuals with neurofibromatosis type 1 (NF1).

D. Gutmann, A. Guha, K. North, 2002, Neurology.

Association of Alzheimer Disease With Life Expectancy in People With Down Syndrome

O. Plana-Ripoll, A. Lleó, O. Belbin, 2022, JAMA network open.

Festschrift for Victor A. McKusick on the Centenary of his Birth: Introduction

A. Hamosh, S. Rasmussen, 2021, American journal of medical genetics. Part A.

NF1 mutation analysis using a combined heteroduplex/SSCP approach

D. J. Driscoll, M. Wallace, S. Rasmussen, 1997, Human mutation.

The influence of selection bias on identifying an association between allergy medication use and SARS-CoV-2 infection

M. Atkinson, S. Rasmussen, S. Filipp, 2021, EClinicalMedicine.

deletions in neurofibromatosis type 1 . Constitutional and mosaic large NF 1 gene

C. R. Abernathy, C. Schwartz, S. Colman, 2022 .

Prevalence of Select New Symptoms and Conditions Among Persons Aged Younger Than 20 Years and 20 Years or Older at 31 to 150 Days After Testing Positive or Negative for SARS-CoV-2

L. Cowell, B. Jackson, W. Trick, 2022, JAMA network open.

A multiplex-PCR test for EVI2A and EVI2B polymorphisms within the human NF1 gene

S. Colman, M. Wallace, S. Rasmussen, 1996, Mammalian Genome.

Prevalence of 22q11 region deletions in patients with velopharyngeal insufficiency.

D. J. Driscoll, C. Williams, F. Boyar, 1998, American journal of medical genetics.

Online Mendelian Inheritance in Man (OMIM®): Victor McKusick's magnum opus

Carol A. Bocchini, A. F. Scott, J. Amberger, 2021, American journal of medical genetics. Part A.

Ectopia cordis, midline defects and chromosome abnormalities: an epidemiologic perspective.

M. Khoury, S. Rasmussen, J. Cordero, 1988, American journal of medical genetics.

NF1 gene and neurofibromatosis 1.

J M Friedman, S. Rasmussen, S. Rasmussen, 2000, American journal of epidemiology.

Analysis of CpG C‐to‐T mutations in neurofibromatosis type 1

D. J. Driscoll, F. Collins, M. Wallace, 1998, Human mutation.

Segregation of a familial balanced (12;10) insertion resulting in Dup(10)(q21.2q22.1) and Del(10)(q21.2q22.1) in first cousins.

G. Semenza, K. Doheny, M. Schwartz, 1997, American journal of medical genetics.

Descriptive epidemiology of holoprosencephaly and arhinencephaly in metropolitan Atlanta, 1968-1992.

M. Khoury, C. Moore, S. Rasmussen, 1996, American journal of medical genetics.

Culture of cytogenetically abnormal Schwann cells from benign and malignant NF1 tumors

M. Wallace, D. Muir, S. Rasmussen, 2000, Genes, chromosomes & cancer.

Response to Biesecker et al.

C. Bult, J. Lupski, R. Gibbs, 2021, American journal of human genetics.

Viewing Victor McKusick's legacy through the lens of his bibliography

J. Amberger, A. Hamosh, S. Rasmussen, 2021, American journal of medical genetics. Part A.

Identification of the familial cylindromatosis tumour-suppressor gene

A. Ashworth, S. Seal, M. Stratton, 2000, Nature Genetics.

Partial duplication 1q: report of four patients and review of the literature.

E. Zackai, S. Rasmussen, J. Frías, 1990, American journal of medical genetics.

Mild expression of the Pfeiffer syndrome

S. Rasmussen, J. Frías, 1988, Clinical genetics.

A population‐based study of craniosynostosis in metropolitan Atlanta, 1989–2003

S. Rasmussen, M. Honein, S. Boulet, 2008, American journal of medical genetics. Part A.

Juvenile rheumatoid arthritis in velo-cardio-facial syndrome: coincidence or unusual complication?

C. Williams, S. Rasmussen, E. Ayoub, 1996, American journal of medical genetics.

A new hereditary cylindromatosis family associated with CYLD1 on chromosome 16

M. Wallace, S. Rasmussen, J. Zhang, 1999, Human Genetics.

Evaluation of birth defect histories obtained through maternal interviews.

M. Khoury, E. K. Maloney, S. Rasmussen, 1990, American journal of human genetics.

Prevalence and descriptive epidemiology of Turner syndrome in the United States, 2000–2017: A report from the National Birth Defects Prevention Network

R. Stevenson, A. Lin, S. Rasmussen, 2023, American journal of medical genetics. Part A.

Middle East Respiratory Syndrome (MERS)

D. Swerdlow, S. Rasmussen, Amelia K. Watson, 2016 .