William H. Schultz

3.3k total citations
50 papers, 2.1k citations indexed

About

William H. Schultz is a scholar working on Genetics, Hematology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, William H. Schultz has authored 50 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Genetics, 35 papers in Hematology and 12 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in William H. Schultz's work include Hemoglobinopathies and Related Disorders (42 papers), Iron Metabolism and Disorders (24 papers) and Blood groups and transfusion (17 papers). William H. Schultz is often cited by papers focused on Hemoglobinopathies and Related Disorders (42 papers), Iron Metabolism and Disorders (24 papers) and Blood groups and transfusion (17 papers). William H. Schultz collaborates with scholars based in United States, Australia and Canada. William H. Schultz's co-authors include Russell E. Ware, Sherri A. Zimmerman, Nicole A. Mortier, Thomas R. Kinney, Thad A. Howard, Jacqueline S. Davis, Howard C. Filston, Banu Aygün, Pamela B. Sylvestre and Ronald W. Helms and has published in prestigious journals such as Journal of Biological Chemistry, Blood and PEDIATRICS.

In The Last Decade

William H. Schultz

50 papers receiving 2.0k citations

Peers

Countries citing papers authored by William H. Schultz

Since Specialization

Citations

This map shows the geographic impact of William H. Schultz's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by William H. Schultz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites William H. Schultz more than expected).

Fields of papers citing papers by William H. Schultz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by William H. Schultz. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by William H. Schultz. The network helps show where William H. Schultz may publish in the future.

Co-authorship network of co-authors of William H. Schultz

This figure shows the co-authorship network connecting the top 25 collaborators of William H. Schultz. A scholar is included among the top collaborators of William H. Schultz based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with William H. Schultz. William H. Schultz is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Stroke prevention in Hispanic children with sickle cell anemia: the SACRED trial 2025 ·Blood Advances ·Rosa M. Nieves, Teresa Latham, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Daniel Ramírez, (unknown), (unknown), (unknown), (unknown), Susan E. Stuber, William H. Schultz, Adam Lane, (unknown), Russell E. Ware	3
2	Building capacity to reduce stroke in children with sickle cell anemia in the Dominican Republic: the SACRED trial 2018 ·Blood Advances ·(unknown), Rosa M. Nieves, Teresa Latham, Susan E. Stuber, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Adam Lane, William H. Schultz, (unknown), (unknown), Russell E. Ware	6
3	Pain and other non‐neurological adverse events in children with sickle cell anemia and previous stroke who received hydroxyurea and phlebotomy or chronic transfusions and chelation: Results from the SWiTCH clinical trial 2013 ·American Journal of Hematology ·Ofelia Álvarez, Nancy A. Yovetich, John P. Scott, William Owen, Scott T. Miller, William H. Schultz, Alexandre Lockhart, Banu Aygün, Jonathan M. Flanagan, Melanie J. Bonner, Brigitta U. Mueller, Russell E. Ware	39
4	Bone marrow transplant options and preferences in a sickle cell anemia cohort on chronic transfusions 2011 ·Pediatric Blood & Cancer ·(unknown), William H. Schultz, Russell E. Ware, Banu Aygün	27
5	R-spondin-1 Is a Novel β-Cell Growth Factor and Insulin Secretagogue 2010 ·Journal of Biological Chemistry ·V. Wong, (unknown), William H. Schultz, Patricia L. Brubaker	27
6	Hydroxyurea therapy lowers transcranial Doppler flow velocities in children with sickle cell anemia 2007 ·Blood ·Sherri A. Zimmerman, William H. Schultz, (unknown), Nicole A. Mortier, Russell E. Ware	149
7	Prevention of secondary stroke and resolution of transfusional iron overload in children with sickle cell anemia using hydroxyurea and phlebotomy 2004 ·The Journal of Pediatrics ·Russell E. Ware, Sherri A. Zimmerman, Pamela B. Sylvestre, Nicole A. Mortier, Jacqueline S. Davis, William R. Treem, William H. Schultz	113
8	Subclinical Parvovirus B19 Infection in Children With Sickle Cell Anemia 2003 ·Journal of Pediatric Hematology/Oncology ·Sherri A. Zimmerman, Jacqueline S. Davis, William H. Schultz, Russell E. Ware	19
9	Malignancy in patients with sickle cell disease 2003 ·American Journal of Hematology ·William H. Schultz, Russell E. Ware	68
10	An Infant With Homozygous Hemoglobin D-Iran 2001 ·The American journal of pediatric hematology/oncology ·Courtney D. Thornburg, Sherri A. Zimmerman, William H. Schultz, Russell E. Ware	7
11	Risky Behavior in Teens With Cystic Fibrosis or Sickle Cell Disease: A Multicenter Study 1998 ·PEDIATRICS ·Maria T. Britto, Joanne M. Garrett, (unknown), C.W. Daeschner, (unknown), Margaret W. Leigh, Joseph M. Majure, William H. Schultz, Thomas R. Konrad	110
12	Successful surgical outcome in children with sickle hemoglobinopathies: The duke university experience 1998 ·Journal of Pediatric Surgery ·Denise M. Adams, Russell E. Ware, William H. Schultz, Allison Kinder Ross, Keith T. Oldham, Thomas R. Kinney	16
13	Quantitative analysis of erythrocytes containing fetal hemoglobin (F cells) in children with sickle cell disease 1997 ·American Journal of Hematology ·(unknown), Thomas R. Kinney, William H. Schultz, Erin E. O’Branski, Russell E. Ware	46
14	Erythrocytapheresis Can Reduce Iron Overload and Prevent the Need for Chelation Therapy in Chronically Transfused Pediatric Patients 1996 ·Journal of Pediatric Hematology/Oncology ·Denise M. Adams, William H. Schultz, Russell E. Ware, T R Kinney	54
15	Hemoglobin C disease in infancy and childhood☆☆☆★★★ 1994 ·The Journal of Pediatrics ·Janice F. Olson, Russell E. Ware, William H. Schultz, T R Kinney	8
16	Diagnosis and management of common bile duct stones in patients with sickle hemoglobinopathies 1992 ·Journal of Pediatric Surgery ·Russell E. Ware, William H. Schultz, Howard C. Filston, Thomas R. Kinney	41
17	Long-term management of splenic sequestration in children with sickle cell disease 1990 ·The Journal of Pediatrics ·Thomas R. Kinney, (unknown), William H. Schultz, Howard C. Filston	60
18	Prolonged use of an implantable central venous access system in a child with severe hemophilia 1989 ·The Journal of Pediatrics ·William H. Schultz, Russell E. Ware, Howard C. Filston, Thomas R. Kinney	14
19	Elective Cholecystectomy in Children with Sickle Hemoglobinopathies 1988 ·Annals of Surgery ·Russell E. Ware, Howard C. Filston, William H. Schultz, Thomas R. Kinney	71
20	Severe neutropenia caused by copper deficiency in a child receiving continuous ambulatory peritoneal dialysis 1986 ·The Journal of Pediatrics ·David L. Becton, William H. Schultz, Thomas R. Kinney	14

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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