| Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome D Liaw, DJ Marsh, J Li, PLM Dahia, SI Wang, Z Zheng, S Bose, KM Call, ... Nature genetics 16 (1), 64-67, 1997 | 2539 | 1997 |
| Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus KM Call, T Glaser, CY Ito, AJ Buckler, J Pelletier, DA Haber, EA Rose, ... Cell 60 (3), 509-520, 1990 | 2461 | 1990 |
| High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones P Lichter, CJ Tang, K Call, G Hermanson, GA Evans, D Housman, ... Science 247 (4938), 64-69, 1990 | 1695 | 1990 |
| Alternative splicing and genomic structure of the Wilms tumor gene WT1. DA Haber, RL Sohn, AJ Buckler, J Pelletier, KM Call, DE Housman Proceedings of the National Academy of Sciences 88 (21), 9618-9622, 1991 | 822 | 1991 |
| An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor DA Haber, AJ Buckler, T Glaser, KM Call, J Pelletier, RL Sohn, ... Cell 61 (7), 1257-1269, 1990 | 713 | 1990 |
| Complete physical map of the WAGR region of 11p13 localizes a candidate Wilms' tumor gene EA Rose, T Glaser, C Jones, CL Smith, WH Lewis, KM Call, M Minden, ... Cell 60 (3), 495-508, 1990 | 335 | 1990 |
| Sequence analysis and functional characterization of the violacein biosynthetic pathway from Chromobacterium violaceum PR August, TH Grossman, C Minor, MP Draper, IA MacNeil, ... Journal of molecular microbiology and biotechnology 2 (4), 513-519, 2000 | 202 | 2000 |
| Evidence for WT1 as a Wilms tumor (WT) gene: intragenic germinal deletion in bilateral WT. V Huff, H Miwa, DA Haber, KM Call, D Housman, LC Strong, GF Saunders American journal of human genetics 48 (5), 997, 1991 | 200 | 1991 |
| Cloning and characterization of a 3-methyladenine DNA glycosylase cDNA from human cells whose gene maps to chromosome 16. L Samson, B Derfler, M Boosalis, K Call Proceedings of the National Academy of Sciences 88 (20), 9127-9131, 1991 | 181 | 1991 |
| Allelic imbalance, including deletion of PTEN/MMAC1, at the Cowden disease locus on 10q22‐23, in hamartomas from patients with cowden syndrome and germline PTEN mutation DJ Marsh, PLM Dahia, V Coulon, Z Zheng, F Dorion‐Bonnet, KM Call, ... Genes, Chromosomes and Cancer 21 (1), 61-69, 1998 | 126 | 1998 |
| Cadmium-induced expression of immediate early genes in LLC-PK1 cells M Matsuoka, KM Call Kidney international 48 (2), 383-389, 1995 | 122 | 1995 |
| Wilms' tumor gene, WT1, mRNA is down-regulated during induction of erythroid and megakaryocytic differentiation of K562 cells SA Phelan, C Lindberg, KM Call Cell Growth and Differentiation-Publication American Association for Cancer …, 1994 | 119 | 1994 |
| Localization and characterization of the Wilms' tumor gene KM Call, TM Glaser, CY Ito, AJ Buckler, J Pelletier, DA Haber, EA Rose, ... US Patent 5,350,840, 1994 | 98 | 1994 |
| Finding genes in the C2C12 osteogenic pathway by k-nearest-neighbor classification of expression data R 5) Theilhaber, J., Connolly, T., Roman-Roman, S., Bushnell, S., Jackson, A ... Genome Research 12 (1), 165-176, 2002 | 90 | 2002 |
| Behavior of osteoblast, adipocyte, and myoblast markers in genome-wide expression analysis of mouse calvaria primary osteoblasts in vitro T Garcia, S Roman-Roman, A Jackson, J Theilhaber, T Connolly, ... Bone 31 (1), 205-211, 2002 | 85 | 2002 |
| Identification of genes regulated during osteoblastic differentiation by genome-wide expression analysis of mouse calvaria primary osteoblasts in vitro S Roman-Roman, T Garcia, A Jackson, J Theilhaber, G Rawadi, ... Bone 32 (5), 474-482, 2003 | 84 | 2003 |
| A genetic linkage map of 27 loci from PND to FY on the short arm of human chromosome I. NC Dracopoli, BZ Stanger, CY Ito, KM Call, SE Lincoln, ES Lander, ... American journal of human genetics 43 (4), 462, 1988 | 79 | 1988 |
| Molecular and biochemical analyses of spontaneous and X-ray induced mutants in human lymphoblastoid cells HL Liber, KM Call, JB Little Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 178 (1 …, 1987 | 74 | 1987 |
| Smallest region of overlap in Wilms tumor deletions uniquely implicates an 11p13 zinc finger gene as the disease locus CCT Ton, V Huff, KM Call, S Cohn, LC Strong, DE Housman, ... Genomics 10 (1), 293-297, 1991 | 63 | 1991 |
| Direct pulsed field gel electrophoresis of Wilms' tumors shows that DNA deletions in 11 p 13 are rare B Royer‐Pokora, S Ragg, B Heckl‐Östreicher, M Held, U Loos, K Call, ... Genes, Chromosomes and Cancer 3 (2), 89-100, 1991 | 49 | 1991 |
