Jane S. Hankins - Concepedia

Author

Jane S. Hankins

St. Jude Children's Research Hospital ORCID

Also Known As

Ataga, K.I, Atlanta Ga, Drossman, Douglas A., J Hankins, J. Hankins, J. S Hankins, J. S. Hankins, J.S. Hankins, Jane Hankins, Jane S Hankins

403

Publications

7.4K

Citations

H-Index

174

Concepts

All Affiliations

St. Jude Children's Research Hospital University of Tennessee Health Science Center Washington University in St. Louis University of Alabama at Birmingham University of Illinois Chicago

About

Jane S. Hankins is an author at St. Jude Children's Research Hospital specializing in medicine, pediatrics, and hematology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	22	33	1.6K
2	Public Health	10	10	436
3	Health Sciences	8	8	533
4	Education	2	2	49
5	Arts	1	1	15

Jane S. Hankins

127

Publications

5.9K

Citations

H-Index

Page 1

	Year	Citations
R2* magnetic resonance imaging of the liver in patients with iron overload Jane S. Hankins, M. Beth McCarville, Ralf B. Loeffler, Blood	2009	370
Long-term hydroxyurea therapy for infants with sickle cell anemia: the HUSOFT extension study Jane S. Hankins, Russell E. Ware, Zora R. Rogers, Blood	2005	286
Streptococcus pneumoniae Translocates into the Myocardium and Forms Unique Microlesions That Disrupt Cardiac Function Armand Brown, Beth Mann, Geli Gao, PLoS Pathogens Cardiac MuscleMicrobial PathogensImmunologyPathologyMicroscopic Lesions	2014	193
Effect of donor type and conditioning regimen intensity on allogeneic transplantation outcomes in patients with sickle cell disease: a retrospective multicentre, cohort study Mary Eapen, Ruta Brazauskas, Mark C. Walters, The Lancet Haematology TransplantationSickle Cell DiseaseHematologyGraft SurvivalBlood Transplantation	2019	192
What Patients Know About Irritable Bowel Syndrome (IBS) and What They Would Like to Know. National Survey on Patient Educational Needs in IBS and Development and Validation of the Patient Educational Needs Questionnaire (PEQ) Albena Halpert, Christine B. Dalton, Olafur S. Palsson, The American Journal of Gastroenterology	2007	178
The effect of hydroxcarbamide therapy on survival of children with sickle cell disease Clarisse Lopes de Castro Lobo, Jorge Francisco da Cunha Pinto, Emília Matos do Nascimento, British Journal of Haematology	2013	160
CRISPR-Cas9 Editing of the <i>HBG1</i> and <i>HBG2</i> Promoters to Treat Sickle Cell Disease Akshay Sharma, Jaap Jan Boelens, Maria Cancio, New England Journal of Medicine	2023	138
Fetal haemoglobin levels and haematological characteristics of compound heterozygotes for haemoglobin S and deletional hereditary persistence of fetal haemoglobin Duyen Ngo, Banu Aygün, Idowu Akinsheye, British Journal of Haematology	2011	128
Glomerular hyperfiltration and albuminuria in children with sickle cell anemia Banu Aygün, Nicole A. Mortier, Matthew P. Smeltzer, Pediatric Nephrology GlomerulonephritisRenal FunctionPediatric HematologyMedicineKidney Failure	2011	126
A Very Low-Carbohydrate Diet Improves Symptoms and Quality of Life in Diarrhea-Predominant Irritable Bowel Syndrome Gregory L. Austin, Christine B. Dalton, Yuming Hu, Clinical Gastroenterology and Hepatology NutritionFood IntoleranceFunctional Gastrointestinal DisorderFood DigestionClinical Nutrition	2009	121

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