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Plos One|December 24, 2014
Extent of non-publication in cohorts of studies approved by research ethics committees or included in trial registriesChristine Schmucker, Lisa K Schell, Susan Portalupi, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 21, 2017
Association of IMMP2L deletions with autism spectrum disorder: A trio family study and meta-analysisYanqing Zhang, Yi Liu, Mehdi Zarrei, et al.
Fertility and Sterility|January 28, 2014
Development of a high-resolution Y-chromosome microarray for improved male infertility diagnosisRyan K C Yuen, Anna Merkoulovitch, Jeffrey R MacDonald, et al.
Scientific Reports|July 27, 2025
Genetic findings of children with congenital heart diseases using chromosomal microarray and trio-based whole exome sequencingRui Guo, Chunhong Duan, Mehdi Zarrei, et al.
American Journal of Medical Genetics. Part A|January 21, 2021
Sleep phenotype of individuals with autism spectrum disorder bearing mutations in the PER2 circadian rhythm geneNy Hoang, Ryan K C Yuen, Jennifer Howe, et al.
Human Molecular Genetics|May 1, 1996
Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb developmentM A Crackower, S W Scherer, J M Rommens, et al.
Genes, Chromosomes & Cancer|November 7, 2000
t(7;12)(q36;p13), a new recurrent translocation involving ETV6 in infant leukemiaS Tosi, J Harbott, A Teigler-Schlegel, et al.
Physical Review Letters|August 30, 2021
Pressure-Induced Excitations in the Out-of-Plane Optical Response of the Nodal-Line Semimetal ZrSiSJ Ebad-Allah, S Rojewski, M Vöst, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 18, 1998
Cloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuriaD Leclerc, A Wilson, R Dumas, et al.
Nature Genetics|March 1, 1993
Physical mapping of the holoprosencephaly critical region on chromosome 7q36F Gurrieri, B J Trask, G van den Engh, et al.
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