| Year |
Citation |
Score |
| 2020 |
Cruz-Aviles LM, Bale A, Carpenter TO. SAT-065 A Novel De Novo GATA3 Gene Mutation in an Adolescent with HDR Syndrome Journal of the Endocrine Society. 4. DOI: 10.1210/Jendso/Bvaa046.1845 |
0.31 |
|
| 2019 |
Phatak A, Athar M, Crowell JA, Leffel D, Herbert BS, Bale AE, Kopelovich L. Global gene expression of histologically normal primary skin cells from BCNS subjects reveals "single-hit" effects that are influenced by rapamycin. Oncotarget. 10: 1360-1387. PMID 30858923 DOI: 10.18632/Oncotarget.26640 |
0.398 |
|
| 2019 |
Jaime Villalonga A, Bale A, Smith M, Majumdar S. SAT-082 Severe Hypertriglyceridemia Associated with a PRKAA1 Gene Mutation Coding for the Alpha1-Subunit of AMPK Journal of the Endocrine Society. 3. DOI: 10.1210/Js.2019-Sat-082 |
0.333 |
|
| 2018 |
Penque BA, Su L, Wang J, Ji W, Bale A, Luh F, Fulbright RK, Sarmast U, Sega AG, Konstantino M, Spencer-Manzon M, Pierce R, Yen Y, Lakhani SA. A homozygous variant in RRM2B is associated with severe metabolic acidosis and early neonatal death. European Journal of Medical Genetics. PMID 30439532 DOI: 10.1016/J.Ejmg.2018.11.008 |
0.425 |
|
| 2018 |
Jeffries L, Olivieri JE, Ji W, Spencer-Manzon M, Bale A, Konstantino M, Lakhani SA. Two siblings with a novel nonsense variant provide further delineation of the spectrum of recessive KLHL7 diseases. European Journal of Medical Genetics. PMID 30300710 DOI: 10.1016/J.Ejmg.2018.10.003 |
0.378 |
|
| 2018 |
Gulati A, Bale AE, Dykas DJ, Bia MJ, Danovitch GM, Moeckel GW, Somlo S, Dahl NK. TREX1 Mutation Causing Autosomal Dominant Thrombotic Microangiopathy and CKD-A Novel Presentation. American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation. PMID 29941221 DOI: 10.1053/J.Ajkd.2018.05.006 |
0.376 |
|
| 2018 |
Shevell LM, Lee E, Dhodapkar R, Dykas D, Popa A, Ma D, Bar N, Baluha A, Burns AJ, Ochoa Chaar CI, Dupont A, Gu S, Halene S, Luciano R, Marien R, ... ... Bale A, et al. Whole Exome Sequencing and Extended Thrombophilia Testing in Patients with Venous Thromboembolism Blood. 132: 2506-2506. DOI: 10.1182/Blood-2018-99-115529 |
0.4 |
|
| 2017 |
Lee EJ, Dykas DJ, Leavitt AD, Camire RM, Ebberink E, García de Frutos P, Gnanasambandan K, Gu SX, Huntington JA, Lentz SR, Mertens K, Parish CR, Rezaie AR, Sayeski PP, Cromwell C, ... ... Bale AE, et al. Whole-exome sequencing in evaluation of patients with venous thromboembolism. Blood Advances. 1: 1224-1237. PMID 29296762 DOI: 10.1182/Bloodadvances.2017005249 |
0.356 |
|
| 2017 |
Couto PP, Bastos-Rodrigues L, Schayek H, Melo FM, Lisboa RGC, Miranda DM, Vilhena A, Bale AE, Friedman E, De Marco L. Spectrum of germline mutations in smokers and non-smokers in Brazilian non-small lung cancer (NSCLC) patients. Carcinogenesis. PMID 28968711 DOI: 10.1093/Carcin/Bgx089 |
0.406 |
|
| 2016 |
Melo FM, Couto PP, Bale AE, Bastos-Rodrigues L, Passos FM, Lisboa RG, Ng JM, Curran T, Dias EP, Friedman E, De Marco L. Whole-exome identifies RXRG and TH germline variants in familial isolated prolactinoma. Cancer Genetics. PMID 27245436 DOI: 10.1016/J.Cancergen.2016.05.065 |
0.396 |
|
| 2016 |
Ziai J, Matloff E, Choi J, Kombo N, Materin M, Bale AE. Defining the polyposis/colorectal cancer phenotype associated with the Ashkenazi GREM1 duplication: counselling and management recommendations. Genetics Research. 98: e5. PMID 26947005 DOI: 10.1017/S0016672316000021 |
0.412 |
|
| 2015 |
Berlin NL, Cartmel B, Leffell DJ, Bale AE, Mayne ST, Ferrucci LM. Family history of skin cancer is associated with early-onset basal cell carcinoma independent of MC1R genotype. Cancer Epidemiology. 39: 1078-83. PMID 26381319 DOI: 10.1016/J.Canep.2015.09.005 |
0.328 |
|
| 2015 |
Ziganshin BA, Bailey AE, Coons C, Dykas D, Charilaou P, Tanriverdi LH, Liu L, Tranquilli M, Bale AE, Elefteriades JA. Routine Genetic Testing for Thoracic Aortic Aneurysm and Dissection in a Clinical Setting. The Annals of Thoracic Surgery. 100: 1604-11. PMID 26188975 DOI: 10.1016/J.Athoracsur.2015.04.106 |
0.358 |
|
| 2015 |
Lee E, Dykas D, Bale A, Cromwell C, Parker TL, Halene S, Burns A, Yao X, Lee AI. Whole Exome Sequencing in Evaluation of Thrombophilia: A Novel 33-Gene Panel Blood. 126: 3529-3529. DOI: 10.1182/Blood.V126.23.3529.3529 |
0.328 |
|
| 2014 |
Cartmel B, Dewan A, Ferrucci LM, Gelernter J, Stapleton J, Leffell DJ, Mayne ST, Bale AE. Novel gene identified in an exome-wide association study of tanning dependence. Experimental Dermatology. 23: 757-9. PMID 25041255 DOI: 10.1111/Exd.12503 |
0.355 |
|
| 2014 |
Carneiro JG, Couto PG, Bastos-Rodrigues L, Bicalho MA, Vidigal PV, Vilhena A, Amaral NF, Bale AE, Friedman E, De Marco L. Spectrum of somatic EGFR, KRAS, BRAF, PTEN mutations and TTF-1 expression in Brazilian lung cancer patients. Genetics Research. 96: e002. PMID 24594201 DOI: 10.1017/S0016672314000032 |
0.373 |
|
| 2012 |
Petty EM, Glynn M, Bale AE. Direct molecular diagnosis of multiple endocrine neoplasia type 1. Methods in Molecular Medicine. 49: 227-42. PMID 21370144 DOI: 10.1385/1-59259-081-0:227 |
0.363 |
|
| 2012 |
Shifrin AL, Bale AE, Dykas D, Fay AM, Belitsis K, Fomin S, Lann D, Villanueva R, Zheng M, Govil S, Erler B, Matulewicz T, Topilow A, Krasna M, Vernick J. MEN1 gene mutations with different phenotypic presentations in two families: Is it a time to grade MEN1 mutations as high-risk and low-risk? Journal of Clinical Oncology. 30: 1540-1540. DOI: 10.1200/Jco.2012.30.15_Suppl.1540 |
0.443 |
|
| 2012 |
Ferrucci LM, Cartmel B, Molinaro AM, Leffell DJ, Bale AE, Mayne ST. Abstract 635: Indoor tanning and risk of early-onset basal cell carcinoma Cancer Research. 72: 635-635. DOI: 10.1158/1538-7445.Am2012-635 |
0.304 |
|
| 2011 |
Wang NJ, Sanborn Z, Arnett KL, Bayston LJ, Liao W, Proby CM, Leigh IM, Collisson EA, Gordon PB, Jakkula L, Pennypacker S, Zou Y, Sharma M, North JP, Vemula SS, ... ... Bale AE, et al. Loss-of-function mutations in Notch receptors in cutaneous and lung squamous cell carcinoma. Proceedings of the National Academy of Sciences of the United States of America. 108: 17761-6. PMID 22006338 DOI: 10.1073/Pnas.1114669108 |
0.397 |
|
| 2011 |
Williams SA, Wilson JB, Clark AP, Mitson-Salazar A, Tomashevski A, Ananth S, Glazer PM, Semmes OJ, Bale AE, Jones NJ, Kupfer GM. Functional and physical interaction between the mismatch repair and FA-BRCA pathways. Human Molecular Genetics. 20: 4395-410. PMID 21865299 DOI: 10.1182/Blood.V116.21.3370.3370 |
0.416 |
|
| 2009 |
Kottemann MC, Bale AE. Characterization of DNA damage-dependent cell cycle checkpoints in a menin-deficient model. Dna Repair. 8: 944-52. PMID 19608464 DOI: 10.1016/J.Dnarep.2009.06.001 |
0.795 |
|
| 2008 |
Marek LR, Kottemann MC, Glazer PM, Bale AE. MEN1 and FANCD2 mediate distinct mechanisms of DNA crosslink repair. Dna Repair. 7: 476-86. PMID 18258493 DOI: 10.1016/J.Dnarep.2007.12.009 |
0.747 |
|
| 2006 |
Busygina V, Bale AE. Multiple endocrine neoplasia type 1 (MEN1) as a cancer predisposition syndrome: clues into the mechanisms of MEN1-related carcinogenesis. The Yale Journal of Biology and Medicine. 79: 105-14. PMID 17940620 |
0.757 |
|
| 2006 |
Cajaiba MM, Bale AE, Alvarez-Franco M, McNamara J, Reyes-Múgica M. Rhabdomyosarcoma, Wilms tumor, and deletion of the patched gene in Gorlin syndrome. Nature Clinical Practice. Oncology. 3: 575-80. PMID 17019435 DOI: 10.1038/Ncponc0608 |
0.304 |
|
| 2006 |
Risch HA, Bale AE, Beck PA, Zheng W. PGR +331 A/G and increased risk of epithelial ovarian cancer. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 15: 1738-41. PMID 16985038 DOI: 10.1158/1055-9965.Epi-06-0272 |
0.308 |
|
| 2006 |
Pejovic T, Yates JE, Liu HY, Hays LE, Akkari Y, Torimaru Y, Keeble W, Rathbun RK, Rodgers WH, Bale AE, Ameziane N, Zwaan CM, Errami A, Thuillier P, Cappuccini F, et al. Cytogenetic instability in ovarian epithelial cells from women at risk of ovarian cancer Cancer Research. 66: 9017-9025. PMID 16982743 DOI: 10.1158/0008-5472.Can-06-0222 |
0.409 |
|
| 2006 |
Busygina V, Kottemann MC, Scott KL, Plon SE, Bale AE. Multiple endocrine neoplasia type 1 interacts with forkhead transcription factor CHES1 in DNA damage response. Cancer Research. 66: 8397-403. PMID 16951149 DOI: 10.1158/0008-5472.Can-06-0061 |
0.758 |
|
| 2006 |
Klein RD, Thorland EC, Gonzales PR, Beck PA, Dykas DJ, McGrath JM, Bale AE. A multiplex assay for the detection and mapping of complex glycerol kinase deficiency. Clinical Chemistry. 52: 1864-70. PMID 16887896 DOI: 10.1373/Clinchem.2006.072397 |
0.343 |
|
| 2006 |
Marek LR, Bale AE. Drosophila homologs of FANCD2 and FANCL function in DNA repair. Dna Repair. 5: 1317-26. PMID 16860002 DOI: 10.1016/J.Dnarep.2006.05.044 |
0.794 |
|
| 2006 |
Yamaguchi S, Brailey LL, Morizono H, Bale AE, Tuchman M. Mutations and polymorphisms in the human ornithine transcarbamylase (OTC) gene. Human Mutation. 27: 626-32. PMID 16786505 DOI: 10.1002/Humu.20339 |
0.426 |
|
| 2005 |
Klein RD, Dykas DJ, Bale AE. Clinical testing for the nevoid basal cell carcinoma syndrome in a DNA diagnostic laboratory. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 7: 611-9. PMID 16301862 DOI: 10.1097/01.Gim.0000182879.57182.B4 |
0.426 |
|
| 2005 |
Cooper AF, Yu KP, Brueckner M, Brailey LL, Johnson L, McGrath JM, Bale AE. Cardiac and CNS defects in a mouse with targeted disruption of suppressor of fused. Development (Cambridge, England). 132: 4407-17. PMID 16155214 DOI: 10.1242/Dev.02021 |
0.373 |
|
| 2005 |
Klein RD, Salih S, Bessoni J, Bale AE. Clinical testing for multiple endocrine neoplasia type 1 in a DNA diagnostic laboratory. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 7: 131-8. PMID 15714081 DOI: 10.1097/01.Gim.0000153663.62300.F8 |
0.457 |
|
| 2004 |
Busygina V, Suphapeetiporn K, Marek LR, Stowers RS, Xu T, Bale AE. Hypermutability in a Drosophila model for multiple endocrine neoplasia type 1 Human Molecular Genetics. 13: 2399-2408. PMID 15333582 DOI: 10.1093/Hmg/Ddh271 |
0.754 |
|
| 2003 |
Kim S, Rimm D, Carter D, Khan A, Parisot N, Franco MA, Bale A, Haffty BG. BRCA status, molecular markers, and clinical variables in early, conservatively managed breast cancer. The Breast Journal. 9: 167-74. PMID 12752624 DOI: 10.1046/J.1524-4741.2003.09307.X |
0.357 |
|
| 2002 |
Suphapeetiporn K, Greally JM, Walpita D, Ashley T, Bale AE. MEN1 tumor-suppressor protein localizes to telomeres during meiosis. Genes, Chromosomes & Cancer. 35: 81-5. PMID 12203793 DOI: 10.1002/Gcc.10113 |
0.676 |
|
| 2002 |
Bale AE. Hedgehog signaling and human disease. Annual Review of Genomics and Human Genetics. 3: 47-65. PMID 12142354 DOI: 10.1146/Annurev.Genom.3.022502.103031 |
0.376 |
|
| 2002 |
Ernest S, Christensen B, Gilfix BM, Mamer OA, Hosack A, Rodier M, Colmenares C, McGrath J, Bale A, Balling R, Sankoff D, Rosenblatt DS, Nadeau JH. Genetic and molecular control of folate-homocysteine metabolism in mutant mice. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 13: 259-67. PMID 12016514 DOI: 10.1007/S00335-001-3054-2 |
0.409 |
|
| 2002 |
Llort G, Muñoz CY, Tuser MP, Guillermo IB, Lluch JR, Bale AE, Franco MA. Low frequency of recurrent BRCA1 and BRCA2 mutations in Spain. Human Mutation. 19: 307. PMID 11857748 DOI: 10.1002/Humu.9014 |
0.372 |
|
| 2001 |
Bale AE, Yu KP. The hedgehog pathway and basal cell carcinomas. Human Molecular Genetics. 10: 757-62. PMID 11257109 DOI: 10.1093/Hmg/10.7.757 |
0.475 |
|
| 2000 |
Taylor TJ, Donlon SS, Bale AE, Smallridge RC, Francis TB, Christensen RS, Burma KD. Treatment of a thyrotropinoma with octreotide-LAR in a patient with multiple endocrine neoplasia-1. Thyroid : Official Journal of the American Thyroid Association. 10: 1001-7. PMID 11128714 DOI: 10.1089/Thy.2000.10.1001 |
0.304 |
|
| 2000 |
Barreto DC, Gomez RS, Bale AE, Boson WL, De Marco L. PTCH gene mutations in odontogenic keratocysts. Journal of Dental Research. 79: 1418-22. PMID 10890722 DOI: 10.1177/00220345000790061101 |
0.466 |
|
| 2000 |
Dong J, Gailani MR, Pomeroy SL, Reardon D, Bale AE. Identification of PATCHED mutations in medulloblastomas by direct sequencing. Human Mutation. 16: 89-90. PMID 10874314 DOI: 10.1002/1098-1004(200007)16:1<89::Aid-Humu18>3.0.Co;2-7 |
0.444 |
|
| 1999 |
Wicking C, Smyth I, Bale A. The hedgehog signalling pathway in tumorigenesis and development. Oncogene. 18: 7844-7851. PMID 10630637 DOI: 10.1038/Sj.Onc.1203282 |
0.326 |
|
| 1999 |
Heptulla RA, Schwartz RP, Bale AE, Flynn S, Genel M. Familial medullary thyroid carcinoma: presymptomatic diagnosis and management in children. The Journal of Pediatrics. 135: 327-31. PMID 10484798 DOI: 10.1016/S0022-3476(99)70129-0 |
0.342 |
|
| 1999 |
Petroianu A, Boson WL, Bale AE, Friedman E, De Marco L. Mutational analyses of candidate genes in human squamous cell carcinomas. The Laryngoscope. 109: 661-3. PMID 10201760 DOI: 10.1097/00005537-199904000-00027 |
0.401 |
|
| 1998 |
Wicking C, Bale AE. Molecular basis of the nevoid basal cell carcinoma syndrome. Current Opinion in Pediatrics. 9: 630-5. PMID 9425597 DOI: 10.1097/00008480-199712000-00013 |
0.455 |
|
| 1998 |
Maestri NE, Lord C, Glynn M, Bale A, Brusilow SW. The phenotype of ostensibly healthy women who are carriers for ornithine transcarbamylase deficiency. Medicine. 77: 389-397. DOI: 10.1097/00005792-199811000-00004 |
0.346 |
|
| 1997 |
Gailani MR, Bale AE. Developmental genes and cancer: role of patched in basal cell carcinoma of the skin. Journal of the National Cancer Institute. 89: 1103-9. PMID 9262247 DOI: 10.1093/Jnci/89.15.1103 |
0.477 |
|
| 1997 |
Levanat S, Chidambaram A, Wicking C, Bray-Ward P, Pressman C, Toftgard R, Gailani MR, Myers JC, Wainwright B, Dean M, Bale AE. Pulsed-field gel electrophoresis and FISH mapping of chromosome 9q22: placement of a novel zinc finger gene within the NBCCS and ESS1 region. Cytogenetics and Cell Genetics. 76: 208-13. PMID 9186526 DOI: 10.1159/000134551 |
0.301 |
|
| 1997 |
Kimonis VE, Goldstein AM, Pastakia B, Yang ML, Kase R, Digiovanna JJ, Bale AE, Bale SJ. Clinical manifestations in 105 persons with nevoid basal cell carcinoma syndrome American Journal of Medical Genetics. 69: 299-308. PMID 9096761 DOI: 10.1002/(Sici)1096-8628(19970331)69:3<299::Aid-Ajmg16>3.0.Co;2-M |
0.331 |
|
| 1997 |
Bale AE. The nevoid basal cell carcinoma syndrome: genetics and mechanism of carcinogenesis. Cancer Investigation. 15: 180-6. PMID 9095215 DOI: 10.3109/07357909709115772 |
0.432 |
|
| 1997 |
Chidambaram A, Gailani M, Gerrard B, Stewart C, Goldstein A, Chumakov I, Bale AE, Dean M. Characterization of a YAC contig containing the NBCCS locus and a novel kruppel-type zinc finger sequence on chromosome segment 9q22.3 Genes Chromosomes and Cancer. 18: 212-218. PMID 9071574 DOI: 10.1002/(Sici)1098-2264(199703)18:3<212::Aid-Gcc7>3.0.Co;2-4 |
0.373 |
|
| 1996 |
Hahn H, Wicking C, Zaphiropoulos PG, Gailani MR, Shanley S, Chidambaram A, Vorechovsky I, Holmberg E, Unden AB, Gillies S, Negus K, Smyth I, Pressman C, Leffell DJ, Gerrard B, ... ... Bale AE, et al. Mutations of the human homolog of drosophila patched in the nevoid basal cell carcinoma syndrome Cell. 85: 841-851. PMID 8681379 DOI: 10.1016/S0092-8674(00)81268-4 |
0.44 |
|
| 1996 |
Hahn H, Christiansen J, Wicking C, Zaphiropoulos PG, Chidambaram A, Gerrard B, Vorechovsky I, Bale AE, Toftgard R, Dean M, Wainwright B. A mammalian patched homolog is expressed in target tissues of sonic hedgehog and maps to a region associated with developmental abnormalities Journal of Biological Chemistry. 271: 12125-12128. PMID 8647801 DOI: 10.1074/Jbc.271.21.12125 |
0.342 |
|
| 1996 |
Gailani MR, Leffell DJ, Ziegler A, Gross EG, Brash DE, Bale AE. Relationship between sunlight exposure and a key genetic alteration in basal cell carcinoma. Journal of the National Cancer Institute. 88: 349-54. PMID 8609643 DOI: 10.1093/Jnci/88.6.349 |
0.403 |
|
| 1995 |
PERICAK-VANCE MA, BALE AE, HAINES JL, KWIATKOWSKI DJ, PILZ A, SLAUGENHAUPT S, WHITE JA, EDWARDS JH, MARCHUK D, OLOPADE OI, ATTWOOD J, POVEY S. REPORT on the Fourth International Workshop on Chromosome 9: held at Williamsburg, Virginia, USA, April 23?25, 1995 Annals of Human Genetics. 59: 347-365. DOI: 10.1111/J.1469-1809.1995.Tb00756.X |
0.305 |
|
| 1994 |
Goldstein AM, Pastakia B, DiGiovanna JJ, Poliak S, Santucci S, Kase R, Bale AE, Bale SJ. Clinical findings in two African-American families with the nevoid basal cell carcinoma syndrome (NBCC) American Journal of Medical Genetics. 50: 272-281. PMID 8042672 DOI: 10.1002/Ajmg.1320500311 |
0.344 |
|
| 1994 |
Compton JG, Goldstein AM, Turner M, Bale AE, Kearns KS, McBride OW, Bale SJ. Fine mapping of the locus for nevoid basal cell carcinoma syndrome on chromosome 9q. The Journal of Investigative Dermatology. 103: 178-81. PMID 8040607 DOI: 10.1111/1523-1747.Ep12392682 |
0.356 |
|
| 1994 |
Bale AE, Gailani MR, Leffell DJ. Nevoid Basal Cell Carcinoma Syndrome Journal of Investigative Dermatology. 103. DOI: 10.1038/Jid.1994.23 |
0.428 |
|
| 1994 |
Bale AE. Molecular Mechanisms of Neoplasia in Multiple Endocrine Neoplasia Type 1-Related and Sporadic Tumors of the Pancreatic Islet Cells Endocrinology and Metabolism Clinics of North America. 23: 109-115. DOI: 10.1016/S0889-8529(18)30119-1 |
0.384 |
|
| 1993 |
Ziegler A, Leffell DJ, Kunala S, Sharma HW, Gailani M, Simon JA, Halperin AJ, Baden HP, Shapiro PE, Bale AE, Brash DE. Mutation hotspots due to sunlight in the p53 gene of nonmelanoma skin cancers Proceedings of the National Academy of Sciences of the United States of America. 90: 4216-4220. PMID 8483937 DOI: 10.1073/Pnas.90.9.4216 |
0.421 |
|
| 1993 |
Petty EM, Bolognia JL, Bale AE, Yang-Feng T. Cutaneous malignant melanoma and atypical moles associated with a constitutional rearrangement of chromosomes 5 and 9. American Journal of Medical Genetics. 45: 77-80. PMID 8418665 DOI: 10.1002/Ajmg.1320450119 |
0.365 |
|
| 1992 |
Cannon-Albright LA, Goldgar DE, Meyer LJ, Lewis CM, Anderson DE, Fountain JW, Hegi ME, Wiseman RW, Petty EM, Bale AE, Olopade OI, Diaz MO, Kwiatkowski DJ, Piepkorn MW, Zone JJ, et al. Assignment of a locus for familial melanoma, MLM, to chromosome 9p13-p22 Science. 258: 1148-1152. PMID 1439824 DOI: 10.1126/Science.1439824 |
0.335 |
|
| 1992 |
Mitchell A, Bale AE, Lee BJ, Hatfield D, Harley H, Rundle SA, Fan YS, Fukushima Y, Shows TB, McBride OW. Regional localization of the selenocysteine tRNA gene (TRSP) on human chromosome 19. Cytogenetic and Genome Research. 61: 117-120. PMID 1395717 DOI: 10.1159/000133385 |
0.363 |
|
| 1992 |
Petty EM, Gold E, Bale AE. DNA Diagnosis with Mutation-Specific Artificial Methylation Sites: Application to Rapid Screening of Δ F508 Clinical Chemistry. 38: 2422-2425. DOI: 10.1093/Clinchem/38.12.2422 |
0.364 |
|
| 1991 |
Bale SJ, Amos CI, Parry DM, Bale AE. Relationship between head circumference and height in normal adults and in the nevoid basal cell carcinoma syndrome and neurofibromatosis type I. American Journal of Medical Genetics. 40: 206-210. PMID 1910262 DOI: 10.1002/Ajmg.1320400217 |
0.321 |
|
| 1991 |
Fein HG, Burman KD, Djuh YY, Usala SJ, Bale AE, Weintraub BD, Smallridge RC. Tight linkage of the human c-erbAβ gene with the syndrome of generalized thyroid hormone resistance is present in multiple kindreds Journal of Endocrinological Investigation. 14: 219-223. PMID 1677017 DOI: 10.1007/Bf03346792 |
0.325 |
|
| 1990 |
Friedman E, Bale AE, Marx SJ, Norton JA, Arnold A, Tu T, Aurbach GD, Spiegel AM. Genetic abnormalities in sporadic parathyroid adenomas. The Journal of Clinical Endocrinology and Metabolism. 71: 293-7. PMID 2199477 DOI: 10.1210/Jcem-71-2-293 |
0.34 |
|
| 1990 |
Wong EL, Kandpal G, Bale AE. Two RFLPs at the glutathione S-transferase 3 gene. Nucleic Acids Research. 18: 4964-4964. PMID 1975681 DOI: 10.1093/Nar/18.16.4964 |
0.334 |
|
| 1989 |
Bale SJ, Bale AE, Stewart K, Dachowski L, McBride OW, Glaser T, Green JE, Mulvihill JJ, Brandi ML, Sakaguchi K, Aurbach GD, Marx SJ. Linkage analysis of multiple endocrine neoplasia type 1 with INT2 and other markers on chromosome 11 Genomics. 4: 320-322. PMID 2565877 DOI: 10.1016/0888-7543(89)90336-4 |
0.414 |
|
| 1989 |
Bale AE, Bale SJ, Murli H, Ivett J, Mulvihill JJ, Parry DM. Sister chromatid exchange and chromosome fragility in the nevoid basal cell carcinoma syndrome Cancer Genetics and Cytogenetics. 42: 273-279. PMID 2507127 DOI: 10.1016/0165-4608(89)90095-2 |
0.321 |
|
| 1989 |
Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 922–947 Cytogenetic and Genome Research. 51: 922-947. DOI: 10.1159/000227799 |
0.383 |
|
| 1989 |
Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 892–921 Cytogenetic and Genome Research. 51: 892-921. DOI: 10.1159/000227798 |
0.383 |
|
| 1989 |
Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 862–891 Cytogenetic and Genome Research. 51: 862-891. DOI: 10.1159/000227797 |
0.383 |
|
| 1989 |
Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 832–861 Cytogenetic and Genome Research. 51: 832-861. DOI: 10.1159/000227796 |
0.383 |
|
| 1989 |
Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 807–831 Cytogenetic and Genome Research. 51: 807-831. DOI: 10.1159/000227795 |
0.383 |
|
| 1989 |
Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 782–806 Cytogenetic and Genome Research. 51: 782-806. DOI: 10.1159/000227794 |
0.383 |
|
| 1989 |
Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 758–781 Cytogenetic and Genome Research. 51: 758-781. DOI: 10.1159/000227793 |
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| 1989 |
Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 732–757 Cytogenetic and Genome Research. 51: 732-757. DOI: 10.1159/000227792 |
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| 1989 |
Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 702–731 Cytogenetic and Genome Research. 51: 702-731. DOI: 10.1159/000227791 |
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Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 677–701 Cytogenetic and Genome Research. 51: 677-701. DOI: 10.1159/000227790 |
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| 1989 |
Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 644–676 Cytogenetic and Genome Research. 51: 644-676. DOI: 10.1159/000227789 |
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