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Author/Creator Mills, James L.

1. A Comparison Study of Fixed and Mixed Effect Models for Gene Level Association Studies of Complex Traits. Issue 8 (4th July 2016)

Authors:
Fan, Ruzong; Chiu, Chi‐yang; Jung, Jeesun; Weeks, Daniel E.; Wilson, Alexander F.; Bailey‐Wilson, Joan E.; Amos, Christopher I.; Chen, Zhen; Mills, James L.; Xiong, Momiao
Journal:
Genetic epidemiology
Issue:
Volume 40:Issue 8(2016)
Page Start:
702
Record Type:
Journal Article
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2. A comparison study of multivariate fixed models and Gene Association with Multiple Traits (GAMuT) for next‐generation sequencing. Issue 1 (5th December 2016)

Authors:
Chiu, Chi‐Yang; Jung, Jeesun; Wang, Yifan; Weeks, Daniel E.; Wilson, Alexander F.; Bailey‐Wilson, Joan E.; Amos, Christopher I.; Mills, James L.; Boehnke, Michael; Xiong, Momiao; Fan, Ruzong
Journal:
Genetic epidemiology
Issue:
Volume 41:Issue 1(2017)
Page Start:
18
Record Type:
Journal Article
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3. A dihydrofolate reductase 2 (DHFR2) variant is associated with risk of neural tube defects in an Irish cohort but not in a United Kingdom cohort. Issue 4 (5th February 2021)

Authors:
Pangilinan, Faith; Finlay, Emma K.; Molloy, Anne M.; Abaan, Hattice O.; Shane, Barry; Mills, James L.; Brody, Lawrence C.; Parle‐McDermott, Anne
Journal:
American journal of medical genetics
Issue:
Volume 185:Issue 4(2021)
Page Start:
1307
Record Type:
Journal Article
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5. Anorectal atresia and Variants at Predicted Regulatory Sites in Candidate Genes. (6th November 2012)

Authors:
Carter, Tonia C.; Kay, Denise M.; Browne, Marilyn L.; Liu, Aiyi; Romitti, Paul A.; Kuehn, Devon; Conley, Mary R.; Caggana, Michele; Druschel, Charlotte M.; Brody, Lawrence C.; Mills, James L.
Journal:
Annals of human genetics
Issue:
Volume 77:Number 1(2013:Jan.)
Page Start:
31
Record Type:
Journal Article
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6. Copy number variants in a population‐based investigation of Klippel–Trenaunay syndrome. Issue 2 (30th November 2016)

Authors:
Dimopoulos, Aggeliki; Sicko, Robert J.; Kay, Denise M.; Rigler, Shannon L.; Fan, Ruzong; Romitti, Paul A.; Browne, Marilyn L.; Druschel, Charlotte M.; Caggana, Michele; Brody, Lawrence C.; Mills, James L.
Journal:
American journal of medical genetics
Issue:
Volume 173:Issue 2(2017)
Page Start:
352
Record Type:
Journal Article
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8. Evaluation of proton‐coupled folate transporter (SLC46A1) polymorphisms as risk factors for neural tube defects and oral clefts. Issue 4 (20th January 2016)

Authors:
VanderMeer, Julia E.; Carter, Tonia C.; Pangilinan, Faith; Mitchell, Adam; Kurnat‐Thoma, Emma; Kirke, Peadar N.; Troendle, James F.; Molloy, Anne M.; Munger, Ronald G.; Feldkamp, Marcia L.; Mansilla, Maria A.; Mills, James L.; Murray, Jeff C.; Brody, Lawrence C.
Journal:
American journal of medical genetics
Issue:
Volume 170:Issue 4(2016)
Page Start:
1007
Record Type:
Journal Article
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9. Exome sequencing identifies variants in infants with sacral agenesis. Issue 7 (10th March 2022)

Authors:
Pitsava, Georgia; Feldkamp, Marcia L.; Pankratz, Nathan; Lane, John; Kay, Denise M.; Conway, Kristin M.; Hobbs, Charlotte; Shaw, Gary M.; Reefhuis, Jennita; Jenkins, Mary M.; Almli, Lynn M.; Moore, Cynthia; Werler, Martha; Browne, Marilyn L.; Cunniff, Chris; Olshan, Andrew F.; Pangilinan, Faith; ...
Other Names:
Brody Lawrence C. investigator.; Browne Marilyn L. investigator.; Feldkamp Marcia L. investigator.; Hobbs Charlotte investigator.; Jenkins Mary M. investigator.; Moore Cynthia investigator.; Olshan Andrew F. investigator.; Reefhuis Jennita investigator.; Romitti Paul A. investigator.; Shaw Gary M...
Journal:
Birth defects research
Issue:
Volume 114:Issue 7(2022)
Page Start:
215
Record Type:
Journal Article
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10. Exome sequencing of child–parent trios with bladder exstrophy: Findings in 26 children. Issue 10 (5th August 2021)

Authors:
Pitsava, Georgia; Feldkamp, Marcia L.; Pankratz, Nathan; Lane, John; Kay, Denise M.; Conway, Kristin M.; Shaw, Gary M.; Reefhuis, Jennita; Jenkins, Mary M.; Almli, Lynn M.; Olshan, Andrew F.; Pangilinan, Faith; Brody, Lawrence C.; Sicko, Robert J.; Hobbs, Charlotte A.; Bamshad, Mike; McGoldrick, ...
Journal:
American journal of medical genetics
Issue:
Volume 185:Issue 10(2021)
Page Start:
3028
Record Type:
Journal Article
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