Struan F.A. Grant - Concepedia

Author

Struan F.A. Grant

Children's Hospital of Philadelphia ORCID

Also Known As

Babette S. Zemel, Bandera, Elisa V., Brian Fulton-Howard, Brown, Christopher D., C. Thivolet, Chai, Jin-Fang, Christian Gieger, Christofidou, P., Donna K. Arnett, Dorret I Boomsma

638

Publications

43.7K

Citations

H-Index

206

Concepts

All Affiliations

Children's Hospital of Philadelphia University of Pennsylvania Harvard University Cincinnati Children's Hospital Medical Center University of Washington

About

Struan F.A. Grant is an author at Children's Hospital of Philadelphia specializing in medicine, genetics, and genetic epidemiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	45	77	13.7K
2	Health Sciences	8	8	933
3	Natural Sciences	3	3	200
4	Education	2	2	76
5	Engineering	1	2	122

Struan F.A. Grant

191

Publications

28.5K

Citations

H-Index

Page 1

	Year	Citations
Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes Struan F.A. Grant, Inga Reynisdóttir, Rafn Benediktsson, Nature Genetics Metabolic SyndromeGenetic DeterminantDiabetes EpidemiologyGeneticsDiabetes	2006	2.3K
PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data Kai Wang, Mingyao Li, Dexter Hadley, Genome Research	2007	1.9K
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes Joseph Glessner, Kai Wang, Guiqing Cai, Nature	2009	1.4K
Common genetic variants on 5p14.1 associate with autism spectrum disorders Kai Wang, Haitao Zhang, Deqiong Ma, Nature Neurodevelopmental DisordersSyndromic AutismGenetic DisorderGeneticsPsychiatric Genetics	2009	968
The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke Anna Helgadóttir, Andrei Manolescu, Sólveig Grétarsdóttir, Nature Genetics InflammationCardiovascular DiseaseBiochemistryAtherosclerosisGenetics	2004	924
A saturated map of common genetic variants associated with human height Loïc Yengo, Sailaja Vedantam, Eirini Marouli, Nature	2022	827
Reduced bone density and osteoporosis associated with a polymorphic Sp1 binding site in the collagen type I α 1 gene Struan F.A. Grant, David Reid, Glen Blake, Nature Genetics Bone DiseaseCollagen TypeReduced Bone DensityGeneticsMolecular Genetics	1996	626
A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene Håkon Håkonarson, Struan F.A. Grant, Jonathan P. Bradfield, Nature Genome-wide Association StudyType 1Genetic DeterminantGeneticsDiabetes	2007	547
Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolution Agnar Helgason, Snæbjörn Pálsson, Struan F.A. Grant, Nature Genetics Metabolic SyndromeAllelic VariantGenetic DeterminantGeneticsDiabetes	2007	527
Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes Josephine Elia, Xiaowu Gai, Hongbo Xie, Molecular Psychiatry GeneticsDisease Gene IdentificationSocial SciencesAdhdAdhd Development	2009	526

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