Year |
Name |
Title |
Published |
1986 |
Mark I. Greene, MD, PhD |
Unavailable |
|
1987 |
No award given |
|
|
1988 |
No award given |
|
|
1989 |
Hiroyuki Shimada, MD |
Pathologic features of extraosseous Ewing’s sarcoma: a report from the Intergroup Rhabdomyosarcoma Study. |
Human Pathology 1988;19:442-453 |
1990 |
Paul S. Thorner, MD, PhD |
Abnormalities of the NCI domain of collagen type IV in GBM in canine hereditary nephritis |
Kidney International 1989;35:843-850 |
1991 |
Beverly Rogers, MD |
Analysis of DNA in fresh and fixed tissue by the polymerase chain reaction. |
Am J Pathol 1990;136:541-548 |
1992 |
David Witte, MD |
Coordinate developmental regulation of purine catabolic enzyme expression in gastrointestinal and postimplantation reproductive tracts. |
J Cell Biology 1991;115:179-190 |
1993 |
Stephen Qualman, MD |
Correlation of neuropeptide expression in tumor tissue with other prognostic factors. |
Cancer 1992;70: 2005-2012 |
1994 |
Poul H Sorensen, MD, PhD |
A second Ewing’s sarcoma translocation t(21;22), fuses the EWS gene to another ETS-family transcription factor ERG. |
Nature Genetics 1994;6:146 |
1995 |
Monique E DePaepe, MD |
The transgenic SAD mouse: a model of human sickle cell glomerulopathy. |
Kid Int. 1994;46: 1337-1345 |
1996 |
No award given |
|
|
1997 |
Raj Kapur, MD, PhD |
Abnormal microenvironmental signals underlie intestinal aganglionosis in Dominant megacolon mutant mice. |
Dev Biol 1996;174:360-369 |
1998 |
Brett Casey, MD |
X-linked situs abnormalities result from mutations in ZIC3 |
Nature Genetics 1997;17:305-308 |
1999 |
No award given |
|
|
2000 |
Anirban Maitra, MD |
The RNA component of telomerase as a marker of biologic potential and clinical outcome in childhood neuroblastic tumors. |
Cancer 1999; 85(3):741-749. |
2001 |
Rusung Tan, MD |
Cutting edge: defective natural killer cell activation in X-linked lymphoproliferative disease |
J Immunol 2000;156:3549 |
2002 |
Jean-Christophe Fournet, MD, PhD |
Unbalanced expression of 11p15 imprinted genes in focal forms of congenital hyperinsulinism. Association with a reduction of homozygosity of a mutation in ABCC8 or KCNJ11. |
Am J Pathol 2002;158:2177 |
2003 |
Csaba Galambos, MD |
Defective Pulmonary Development in the Absence of Heparin-Binding Vascular Endothelial Growth Factor Isoforms |
Am J Respiratory Cell and Mol Biology, 2002;27:194-203. |
2004 |
No award given |
|
|
2005 |
Gail H. Deutsch, MD |
Different thresholds of fibroblast growth factors pattern the ventral foregut into liver and lung |
Development, 2005;132:35-47 |
2006 |
David Horst, MD, Dr. Med. |
Comparative expression analysis of Pax3 and Pax7 during mouse myogenesis |
Int. J. dev. Biol. 2006;50:47-54 |
2007 |
Rene L. Galindo, MD |
A Drosophila model of the rhabdomyosarcoma initiator PAX7-FKHR |
Proc. Natl. Acad. Sci. 2006;103:13439- 13444 |
2008 |
Kudakwashe R. Chikwava, MB., ChB |
Analysis of loss of heterozygosity in single-system and multisystem Langerhan’s cell histiocytosis. |
Pediatr. Dev. Pathol., 2007;10:18-24 |
2009 |
Charles G. Mullighan MBBS(Hons), MSc, MD |
BCR-ABL1 lymphoblastic leukaemia is characterized by the deletion of Ikaros |
Nature 453: 110-4 2008 |
2010 |
Cynthia E. Hawkins, MD |
Whole-Genome Profiling of Pediatric Diffuse Intrinsic Pontine Gliomas Highlights Platelet-Derived Growth Factor Receptor ï•¡ and Poly (ADP-ribose) Polymerase As Potential Therapeutic Targets |
J. Clin. Oncol. 28: 1337-1344, 2010 |
2011 |
Jefferson Terry, MD PhD |
Expression of CD133 in synovial sarcoma. |
Appl Immunohistochem Mol Morphol 18; 159-165, 2010 |
2012 |
Kyle Kurek, MD |
Loss-of-function mutations in PTPN11 cause metachondromatosis, but not Ollier disease or Maffucci syndrome |
PloS Genetics 2011;7(4):e10020500 |
2013 |
Robyn C. Reed, MD |
Symmetrical peripheral gangrene in four pediatric cardiac surgery patients receiving extracorporeal membrane oxygenation. |
Ped Dev Path 2012;15:217-225 |
2014 |
Benjamin Wilkins, MD |
P53-mediated biliary defects caused by knockdown of cirhia, the zebrafish homolog of the gene responsible for North American Indian Childhood cirrhosis. |
PLoS ONE 2013;8(10):e77670 |
2015 |
Erin R Rudzinski, MD |
Myogenin, AP2b, NOS-1, and HMGA2 are surrogate markers of fusion status in rhabdomyosarcoma: a report from the Soft Tissue Sarcoma Committee of the Children’s Oncology Group. |
Am J Surg Pathol 2014;38(5):654-659. |
2016 |
Mariana M Cajaiba, MD |
Pediatric cystic nephromas: distinctive features and frequent DICER1 mutations |
Hum Path 2016;48:81-87 |
2017 |
Miriam Conces, MD |
A strategy for Helicobacter Immunohistochemistry utilization in pediatric practice |
Am J Clin Pathol 2016;145(5): 611- 617 |
2018 |
Ruth Ann Luna, PhD |
Distinct Microbiome-Neuroimmune Signatures Correlate With Functional Abdominal Pain in Children With Autism Spectrum Disorder |
Cell Mol Gastroenterol Hepatol. 2017;3(2):218-230 |
2019 |
Bonnie Cole, MD |
Targeted Sequencing of Malignant Supratentorial Pediatric Brain Tumors Demonstrates a High Frequency of Clinically Relevant Mutations |
Ped Dev Path 2018;21(4):380–388 |
2020 |
Jessica Davis, MD |
Expanding the Spectrum of Pediatric NTRK-rearranged Mesenchymal Tumors |
Am J Surg Pathol. 2019; 43(4): 435-445 |
2021 |
Nya Nelson, MD, PhD |
Mucinous Cell Clusters in Infantile Congenital Pulmonary Airway Malformations Mimic Adult Mucinous Adenocarcinoma But Are Not Associated With Poor Outcomes When Appropriately Resected |
Am J Surg Pathol. 2020 Aug;44(8):1118-1129 |
2022 |
Jennifer Picarsic, MD, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH |
ALK-positive histiocytosis: a new clinicopathologic spectrum highlighting neurologic involvement and responses to ALK inhibition |
|
2023 |
Charlotte F. Kim, MD Texas Children's Hospital
|
Prostatic metaplasia and pilar differentiation in gender-affirming mastectomy specimens |
|
2024 |
Nicholas S. Willard, DO, Children's Hospital Colorado
|
Integration of single‑nuclei RNA‑sequencing, spatial transcriptomics and histochemistry defines the complex microenvironment of NF1‑associated plexiform neurofibromas |
|