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Crossref.
Dick, Danielle M.
Jones, Kevin
Saccone, Nancy
Hinrichs, Anthony
Wang, Jen C.
Goate, Alison
Bierut, Laura
Almasy, Laura
Schuckit, Marc
Hesselbrock, Victor
Tischfield, Jay
Foroud, Tatiana
Edenberg, Howard
Porjesz, Bernice
and
Begleiter, Henri
2006.
Endophenotypes Successfully Lead to Gene Identification: Results from the Collaborative Study on the Genetics of Alcoholism.
Behavior Genetics,
Vol. 36,
Issue. 1,
p.
112.
Roth, Stephen M.
and
Thomis, Martine A.
2011.
Exercise Genomics.
p.
1.
Vicente, Cristina T
Revez, Joana A
and
Ferreira, Manuel A R
2017.
Lessons from ten years of genome‐wide association studies of asthma.
Clinical & Translational Immunology,
Vol. 6,
Issue. 12,
Szabo, Monica
Máté, Beáta
Csép, Katalin
and
Benedek, Theodora
2018.
Genetic Approaches to the Study of Gene Variants and Their Impact on the Pathophysiology of Type 2 Diabetes.
Biochemical Genetics,
Vol. 56,
Issue. 1-2,
p.
22.
Huppertz, Charlotte
de Geus, Eco J. C.
and
van der Ploeg, Hidde P.
2018.
Sedentary Behaviour Epidemiology.
p.
617.
van den Berg, Stéphanie M.
and
de Moor, Marleen H. M.
2020.
Behavior Genetics of Temperament and Personality.
p.
99.
Kimball, Emily E.
and
Sayce, Lea
2020.
Research in Speech Science and Voice Disorders: The Promise of Modern Genetic Approaches in Improving Clinical Diagnosis and Treatment.
Perspectives of the ASHA Special Interest Groups,
p.
1.
Susgun, Seda
Kasan, Koray
and
Yucesan, Emrah
2021.
Gene Hunting Approaches through the Combination of Linkage Analysis with Whole-Exome Sequencing in Mendelian Diseases: From Darwin to the Present Day.
Public Health Genomics,
Vol. 24,
Issue. 5-6,
p.
207.
Clay-Gilmour, Alyssa I.
Camp, Nicola J.
Wei, Xiaomu
Earle, Angel
Norman, Aaron
Sinnwell, Jason
Demangel, Delphine
Griffin, Rosalie
Dumontet, Charles
McKay, James
Offit, Ken
Joseph, Vijai
Chen, Siwei
O’Brien, Daniel
Rajkumar, Vincent
Klein, Robert
Kumar, Shaji
Lipkin, Steve
and
Vachon, Celine M.
2025.
Whole-Exome Sequencing-Based Linkage Analysis of Multiple Myeloma (MM) and Monoclonal Gammopathy of Undetermined Significance (MGUS) Pedigrees.
Cancers,
Vol. 17,
Issue. 22,
p.
3611.