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6,217 authors found
quering by "Congenital disorder"
.
Showing
the first 25
sort by ONE Index.
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912
One Index
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Tolstrup, Janne PhD 0000-0002-9796-3967 |
409 docs (2003 - 2024)
Danish , Alcohol Dependence , Binge drinking , Sitting , Odds |
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903
One Index
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Chung, Wendy PhD 0000-0003-3438-5685 |
1030 docs (1971 - 2024)
Cancer Risk , Exome , cancer susceptibility , Genetic Testing , Breast Cancer |
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901
One Index
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Chong, Jessica PhD 0000-0002-1616-2448 |
122 docs (2011 - 2024)
Exome , Mendelian inheritance , Exome Sequencing , Phenotype Analysis , Genetic Testing |
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896
One Index
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Kurth, Florian PhD 0000-0001-8662-1809 |
99 docs (2009 - 2024)
Meditation , Mindfulness , Gray (unit) , Neuroimaging Data Analysis , Voxel-based morphometry |
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896
One Index
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Anthony, James Christopher (Jim) PhD 0000-0001-7176-0929 |
525 docs (1959 - 2024)
Adolescent Drug Use , Alcohol Dependence , Cannabis Use , drug use , Depression (economics) |
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894
One Index
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Hubbard, Tim @timjph PhD 0000-0002-1767-9318 |
354 docs (1969 - 2024)
Ensembl , genome annotation , Sequence (biology) , Proteins , Pseudogene |
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891
One Index
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Bernstein, Daniel PhD 0000-0001-7761-5853 |
751 docs (1946 - 2024)
Heart Transplant , Transplantation , Elliptic Curves , Cardiotoxicity , Pressure overload |
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890
One Index
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Nelson, Stanley PhD 0000-0002-2082-3114 |
401 docs (1975 - 2024)
Exome , Attention-Deficit/Hyperactivity Disorder , ADHD , Autism , Glioblastoma |
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889
One Index
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Patel, Jenil PhD 0000-0002-4875-7390 |
58 docs (2015 - 2024)
Depression (economics) , Odds , Work-Related Exposure , Clinical Characteristics , Stimulant |
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884
One Index
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Schrier Vergano, Samantha PhD 0000-0001-9194-0644 |
102 docs (2013 - 2024)
Table (database) , Neurodevelopmental disorder , Coffin , Microcephaly , Proband |
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882
One Index
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Glessner, Joseph PhD 0000-0001-5131-2811 |
253 docs (2005 - 2024)
Genome-wide association study , Genetic association , Copy Number Variation , SNP , Candidate gene |
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882
One Index
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Santen, Gijs PhD 0000-0003-1959-3267 |
131 docs (2007 - 2024)
Haploinsufficiency , Exome , ARID1A Mutations , Exome Sequencing , Loss function |
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881
One Index
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Marth, Gabor PhD 0000-0003-0222-1694 |
207 docs (1991 - 2024)
genome annotation , Indel , Exome Sequencing , sequence variation , 1000 Genomes Project |
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881
One Index
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Dobyns, William PhD 0000-0002-7681-2844 |
600 docs (1979 - 2024)
Polymicrogyria , Microcephaly , Cerebellar Malformations , Pachygyria , Brain Development |
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880
One Index
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Shashi, Vandana PhD 0000-0002-5011-7501 |
297 docs (1994 - 2024)
Loss function , Microcephaly , Deletion syndrome , Neurodevelopmental disorder , Brain Development |
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879
One Index
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Isidor, Bertrand PhD 0000-0001-6480-126X |
485 docs (1991 - 2024)
Haploinsufficiency , Microcephaly , Neurodevelopmental disorder , Loss function , Brain Development |
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878
One Index
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Muenke, Maximilian PhD 0000-0002-7719-6545 |
400 docs (1990 - 2024)
Forebrain , Hedgehog Signaling , Craniosynostosis , ADHD , Attention-Deficit/Hyperactivity Disorder |
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878
One Index
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Vorstman, Jacob PhD 0000-0002-1677-3126 |
226 docs (2001 - 2024)
Autism , Deletion syndrome , Copy Number Variation , DiGeorge syndrome , Heritability of autism |
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878
One Index
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Botto, Lorenzo PhD 0000-0002-5322-7116 |
279 docs (1992 - 2024)
Adult Congenital Heart Disease , Congenital Heart Disease , Multivitamin , Gastroschisis , Neural Tube Defects |
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877
One Index
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van Bokhoven, J.H.L.M. (Hans) PhD 0000-0002-2153-9254 |
643 docs (1967 - 2024)
Microcephaly , Haploinsufficiency , Nijmegen breakage syndrome , Fragile X Syndrome , Autism |
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876
One Index
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Agrawal, Pankaj PhD 0000-0003-3255-0456 |
292 docs (1994 - 2024)
Proband , Exome , Clinical Genomics , Exome Sequencing , Neurodevelopmental disorder |
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870
One Index
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Mandel, Jean Louis PhD 0000-0002-0535-6589 |
522 docs (1933 - 2024)
Fragile X Syndrome , Genetic linkage , Adrenoleukodystrophy , Xq28 , FMR1 |
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870
One Index
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Banka, Siddharth PhD 0000-0002-8527-2210 |
300 docs (1969 - 2024)
Haploinsufficiency , Exome Sequencing , Exome , Loss function , Microcephaly |
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869
One Index
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Lyonnet, Stanislas PhD 0000-0001-5426-9417 |
679 docs (1934 - 2024)
Hirschsprung Disease , Hirschsprung's disease , Inborn Errors of Metabolism , RET Gene , Microcephaly |
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869
One Index
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Rauch, Anita PhD 0000-0003-2930-3163 |
358 docs (1964 - 2024)
Haploinsufficiency , Microcephaly , Exome , Brain Development , Exome Sequencing |
