Concepedia

Author

Samantha Caldwell

Sequenom (United States)ORCID

Also Known As

Samantha Caldwell, Samantha L. Caldwell

29

Publications

361

Citations

10

H-Index

31

Concepts

All Affiliations

Sequenom (United States)LabCorp (United States)
SC

About

Samantha Caldwell is an author at Sequenom (United States) specializing in medicine, genetic epidemiology, and biostatistics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

3

3

96

2

Engineering

1

1

16

3

Public Health

1

1

61

4

Social Sciences

1

1

19

5

Behavioral Sciences

1

1

19

Samantha Caldwell

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10

Publications

235

Citations

10

H-Index

YearCitations

Participant use and communication of findings from exome sequencing: a mixed-methods study

Katie L. Lewis, Gillian W. Hooker, Philip D. Connors,

Genetics in Medicine

2015

61

Three years of clinical experience with a genome-wide cfDNA screening test for aneuploidies and copy-number variants

Erica Soster, Theresa Boomer, Susan C. Hicks,

Genetics in Medicine

2021

39

Factors Influencing Time to Determination of the Recommended Phase 2 Dose in Phase 1 Clinical Trials

Samantha Caldwell, Chao Sima, Gayle Jameson,

American Journal of Clinical Oncology

2012

25

Genome-wide cell-free DNA screening: a focus on copy-number variants

Jill M. Rafalko, Erica Soster, Samantha Caldwell,

Genetics in Medicine

2021

24

Executive Functioning and Gambling: Performance on the Trail Making Test is Associated with Gambling Problems in Older Adult Gamblers

William von Hippel, Lily Ng, Laura Abbot,

Aging Neuropsychology and Cognition

2009

19

Impact of mosaicism ratio on positive predictive value of <scp>cfDNA</scp> screening

Jill M. Rafalko, Samantha Caldwell, John A. Tynan,

Prenatal Diagnosis

2020

19

Obesity and no call results: optimal timing of cell-free DNA testing and redraw

Maeve Hopkins, Nathanael Koelper, Samantha Caldwell,

American Journal of Obstetrics and Gynecology

2021

16

Deletion rescue resulting in segmental homozygosity: A mechanism underlying discordant <scp>NIPT</scp> results

Samantha Caldwell, Katelynn G. Sagaser, Zoe Nelson,

American Journal of Medical Genetics Part A

2020

12

Confirmatory testing illustrates additional risks for structural sex chromosome abnormalities in fetuses with a <scp>non‐invasive</scp> prenatal screen positive for monosomy X

Kristen L. Sund, Divya Khattar, Theresa Boomer,

American Journal of Medical Genetics Part C Seminars in Medical Genetics

2020

10

Clinical significance and mechanisms associated with segmental UPD

Peter Papenhausen, Carla A. Kelly, Samuel Harris,

Molecular Cytogenetics

2021

10

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