The Quantitative-MFG Test: A linear mixed effect model to detect maternal-offspring gene interactions

door CLARK, MICHELLE M., BLANGERO, JOHN, DYER, THOMAS D., SOBEL, ERIC M., SINSHEIMER, JANET S.
Gepubliceerd in Ann Hum Genet (2015)

Human Birth Weight and Reproductive Immunology: Testing for Interactions between Maternal and Offspring KIR and HLA-C Genes

door Clark, Michelle M., Chazara, Olympe, Sobel, Eric M., Gjessing, Håkon K., Magnus, Per, Moffett, Ashley, Sinsheimer, Janet S.
Gepubliceerd in Hum Hered (2017)

Meta-analysis of the diagnostic and clinical utility of genome and exome sequencing and chromosomal microarray in children with suspected genetic diseases

door Clark, Michelle M., Stark, Zornitza, Farnaes, Lauge, Tan, Tiong Y., White, Susan M., Dimmock, David, Kingsmore, Stephen F.
Gepubliceerd in NPJ Genom Med (2018)

Partially automated whole-genome sequencing reanalysis of previously undiagnosed pediatric patients can efficiently yield new diagnoses

door James, Kiely N., Clark, Michelle M., Camp, Brandon, Kint, Cyrielle, Schols, Peter, Batalov, Sergey, Briggs, Benjamin, Veeraraghavan, Narayanan, Chowdhury, Shimul, Kingsmore, Stephen F.
Gepubliceerd in NPJ Genom Med (2020)

A Prospective Study of Parental Perceptions of Rapid Whole-Genome and -Exome Sequencing among Seriously Ill Infants

door Cakici, Julie A., Dimmock, David P., Caylor, Sara A., Gaughran, Mary, Clarke, Christina, Triplett, Cynthia, Clark, Michelle M., Kingsmore, Stephen F., Bloss, Cinnamon S.
Gepubliceerd in Am J Hum Genet (2020)

Measurement of genetic diseases as a cause of mortality in infants receiving whole genome sequencing

door Kingsmore, Stephen F., Henderson, Audrey, Owen, Mallory J., Clark, Michelle M., Hansen, Christian, Dimmock, David, Chambers, Christina D., Jeliffe-Pawlowski, Laura L., Hobbs, Charlotte
Gepubliceerd in NPJ Genom Med (2020)

An RCT of Rapid Genomic Sequencing among Seriously Ill Infants Results in High Clinical Utility, Changes in Management, and Low Perceived Harm

door Dimmock, David P., Clark, Michelle M., Gaughran, Mary, Cakici, Julie A., Caylor, Sara A., Clarke, Christina, Feddock, Michele, Chowdhury, Shimul, Salz, Lisa, Cheung, Cynthia, Bird, Lynne M., Hobbs, Charlotte, Wigby, Kristen, Farnaes, Lauge, Bloss, Cinnamon S., Kingsmore, Stephen F.
Gepubliceerd in Am J Hum Genet (2020)

Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalization

door Farnaes, Lauge, Hildreth, Amber, Sweeney, Nathaly M., Clark, Michelle M., Chowdhury, Shimul, Nahas, Shareef, Cakici, Julie A., Benson, Wendy, Kaplan, Robert H., Kronick, Richard, Bainbridge, Matthew N., Friedman, Jennifer, Gold, Jeffrey J., Ding, Yan, Veeraraghavan, Narayanan, Dimmock, David, Kingsmore, Stephen F.
Gepubliceerd in NPJ Genom Med (2018)

The concerted impact of domestication and transposon insertions on methylation patterns between dogs and gray wolves

door Koch, Ilana Janowitz, Clark, Michelle M., Thompson, Michael J., Deere-Machemer, Kerry A., Wang, Jun, Duarte, Lionel, Gnanadesikan, Gitanjali E., McCoy, Eskender L., Rubbi, Liudmilla, Stahler, Daniel R., Pellegrini, Matteo, Ostrander, Elaine A., Wayne, Robert K., Sinsheimer, Janet S., vonHoldt, Bridgett M.
Gepubliceerd in Mol Ecol (2016)

Rapid whole genome sequencing has clinical utility in children in the pediatric intensive care unit

door Sanford, Erica F., Clark, Michelle M., Farnaes, Lauge, Williams, Matthew R., Perry, James C., Ingulli, Elizabeth G., Sweeney, Nathaly M., Doshi, Ami, Gold, Jeffrey J., Briggs, Benjamin, Bainbridge, Matthew N., Feddock, Michele, Watkins, Kelly, Chowdhury, Shimul, Nahas, Shareef A., Dimmock, David P., Kingsmore, Stephen F., Coufal, Nicole G.
Gepubliceerd in Pediatr Crit Care Med (2019)

The NSIGHT1-randomized controlled trial: rapid whole-genome sequencing for accelerated etiologic diagnosis in critically ill infants

door Petrikin, Josh E., Cakici, Julie A., Clark, Michelle M., Willig, Laurel K., Sweeney, Nathaly M., Farrow, Emily G., Saunders, Carol J., Thiffault, Isabelle, Miller, Neil A., Zellmer, Lee, Herd, Suzanne M., Holmes, Anne M., Batalov, Serge, Veeraraghavan, Narayanan, Smith, Laurie D., Dimmock, David P., Leeder, J. Steven, Kingsmore, Stephen F.
Gepubliceerd in NPJ Genom Med (2018)

A Randomized, Controlled Trial of the Analytic and Diagnostic Performance of Singleton and Trio, Rapid Genome and Exome Sequencing in Ill Infants

door Kingsmore, Stephen F., Cakici, Julie A., Clark, Michelle M., Gaughran, Mary, Feddock, Michele, Batalov, Sergey, Bainbridge, Matthew N., Carroll, Jeanne, Caylor, Sara A., Clarke, Christina, Ding, Yan, Ellsworth, Katarzyna, Farnaes, Lauge, Hildreth, Amber, Hobbs, Charlotte, James, Kiely, Kint, Cyrielle I., Lenberg, Jerica, Nahas, Shareef, Prince, Lance, Reyes, Iris, Salz, Lisa, Sanford, Erica, Schols, Peter, Sweeney, Nathaly, Tokita, Mari, Veeraraghavan, Narayanan, Watkins, Kelly, Wigby, Kristen, Wong, Terence, Chowdhury, Shimul, Wright, Meredith S., Dimmock, David
Gepubliceerd in Am J Hum Genet (2019)