Farid Chehab, PhD

Title(s)Professor, Laboratory Medicine
SchoolSchool of Medicine
Address185 Berry Street Bldg B, #1001
San Francisco CA 94158
Phone415-353-4725
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    Collapse Biography 
    Collapse Education and Training
    University of California, San Francisco, CA10/2022Diversity, Equity, and Inclusion Champion Training
    University of California, HHMI, San Francisco, CAFellow1987Molecular Genetics
    American University of Beirut, LebanonPhD1983Molecular Genetics
    American University of Beirut, LebanonMS1979Endocrinology
    American University of Beirut, LebanonBS1976Biology

    Collapse Research 
    Collapse Research Activities and Funding
    Critical CpG Sites of MGMT Promoter in Glioblastoma
    UC Cancer Research Coordinating Committee (CRCC) CRR-19-577975Jan 1, 2019 - Dec 31, 2020
    Role: Principal Investigator
    LEPTIN AND INITIATION OF REPRODUCTIVE FUNCTION
    NIH R01HD035142May 1, 1998 - Apr 30, 2004
    Role: Principal Investigator
    GENE THERAPY STRATEGIES FOR SICKLE CELL DISEASE
    NIH P01HL053762Sep 30, 1994 - Aug 31, 2007
    Role: Co-Investigator
    GENE THERAPY CORE--CYSTIC FIBROSIS &NON-CF GENETIC DIS
    NIH P30DK047766Sep 30, 1993 - Aug 31, 1999
    Role: Co-Investigator

    Collapse ORNG Applications 
    Collapse Academic Senate

    Collapse Bibliographic 
    Collapse Publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. A systematic review of high impact CpG sites and regions for MGMT methylation in glioblastoma [A systematic review of MGMT methylation in GBM]. BMC Neurol. 2024 Mar 23; 24(1):103. Gibson D, Vo AH, Lambing H, Bhattacharya P, Tahir P, Chehab FF, Butowski N. PMID: 38521933; PMCID: PMC10960428.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    2. LNK/SH2B3 as a novel driver in juvenile myelomonocytic leukemia. Haematologica. 2023 Dec 28. Wintering A, Hecht A, Meyer J, Wong EB, Hübner J, Abelson S, Feldman K, Kennedy VE, Peretz CAC, French DL, Maguire JA, Jobaliya C, Vasquez MR, Desai S, Dulman R, Nemecek E, Haines H, Hammad M, El Haddad A, Kogan SC, Abdullaev Z, Chehab FF, Tasian SK, Smith CC, Loh ML, Stieglitz E. PMID: 38152053.
      View in: PubMed   Mentions:    Fields:    
    3. Quantitative analysis of MGMT promoter methylation in glioblastoma suggests nonlinear prognostic effect. Neurooncol Adv. 2023 Jan-Dec; 5(1):vdad115. Gibson D, Ravi A, Rodriguez E, Chang S, Oberheim Bush N, Taylor J, Clarke J, Solomon D, Scheffler A, Witte J, Lambing H, Okada H, Berger M, Chehab F, Butowski NA. PMID: 37899778; PMCID: PMC10611422.
      View in: PubMed   Mentions: 2  
    4. Parietal mass caused by a fish bone: case report. Ann Med Surg (Lond). 2023 Feb; 85(2):299-301. Erguibi D, Kamal K, Eddaoudi Y, Hajri A, Boufettal R, Rifki El Jai S, Chehab F. PMID: 36845793; PMCID: PMC9949763.
      View in: PubMed   Mentions:
    5. LNK/SH2B3 As a Novel Driver in Juvenile Myelomonocytic Leukemia. Blood. 2022 Nov 15; 140(Supplement 1):6863-6864. Wintering WA, Hecht HA, Meyer MJ, Wong WE, French FD, Maguire MJ, Jobaliya JC, Rojas Vasquez RM, Desai DS, Dulman DR, Nemecek NE, Chehab CF, Loh LM, Stieglitz SE. .
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    6. Epidemiology, incidence and treatment of rectal cancer in young women case serie about 11 cases (case series). Ann Med Surg (Lond). 2022 Oct; 82:104693. Hajri A, Fatine A, Eddaoudi Y, Rifki El Jay S, Boufettal R, Erreguibi D, Chehab F. PMID: 36268414; PMCID: PMC9577628.
      View in: PubMed   Mentions:
    7. Molecular and phenotypic diversity of CBL-mutated juvenile myelomonocytic leukemia. Haematologica. 2022 01 01; 107(1):178-186. Hecht A, Meyer JA, Behnert A, Wong E, Chehab F, Olshen A, Hechmer A, Aftandilian C, Bhat R, Choi SW, Chonat S, Farrar JE, Fluchel M, Frangoul H, Han JH, Kolb EA, Kuo DJ, MacMillan ML, Maese L, Maloney KW, Narendran A, Oshrine B, Schultz KR, Sulis ML, Van Mater D, Tasian SK, Hofmann WK, Loh ML, Stieglitz E. PMID: 33375775; PMCID: PMC8719097.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    8. BIOM-07. QUANTITATIVE MGMT PROMOTER METHYLATION INDEX INDICATES A NON-LINEAR PROGNOSTIC EFFECT IN GLIOBLASTOMA, SUGGESTING THAT USE OF OPTIMAL CUTOFF POINTS MAY BE CLINICALLY DISADVANTAGEOUS. Neuro-Oncology. 2021 Nov 12; 23(Supplement_6):vi11-vi11. Gibson GD, Ravi RA, Almaraz AE, Chang CS, Oberheim-Bush ON, Taylor TJ, Clarke CJ, Solomon SD, Scheffler SA, Witte WJ, Lambing LH, Berger BM, Okada OH, Chehab CF, Butowski BN. .
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    9. NGMA-6. Quantitative MGMT Promoter Methylation Index Indicates Non-Linear, Prognostic Effect in Glioblastoma. Neuro-Oncology Advances. 2021 Jul 5; 3(Supplement_2):ii5-ii5. Gibson GD, Ravi RA, Rodriguez RE, Chang CS, Bush BN, Taylor TJ, Clarke CJ, Solomon SD, Scheffler SA, Witte WJ, Okada OH, Berger BM, Chehab CF, Butowski BN. .
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    10. Molecular assessment of pretransplant chemotherapy in the treatment of juvenile myelomonocytic leukemia. Pediatr Blood Cancer. 2019 11; 66(11):e27948. Hecht A, Meyer J, Chehab FF, White KL, Magruder K, Dvorak CC, Loh ML, Stieglitz E. PMID: 31347788; PMCID: PMC6754267.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    11. PAX5, NOTCH3, CBFB, and ACD drive an activated RAS pathway and monosomy 7 to B-ALL and AML in donor cell leukemia. Bone Marrow Transplant. 2019 07; 54(7):1124-1128. Assi R, Mahfouz R, Owen R, Gunthorpe M, Chehab FF, Bazarbachi A. PMID: 30532056.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCellsCTClinical Trials
    12. Upregulation of cholesterol 24-hydroxylase following hypoxia-ischemia in neonatal mouse brain. Pediatr Res. 2018 06; 83(6):1218-1227. Lu F, Zhu J, Guo S, Wong BJ, Chehab FF, Ferriero DM, Jiang X. PMID: 29718007; PMCID: PMC6019156.
      View in: PubMed   Mentions: 11     Fields:    Translation:AnimalsCells
    13. Genome-wide DNA methylation is predictive of outcome in juvenile myelomonocytic leukemia. Nat Commun. 2017 12 19; 8(1):2127. Stieglitz E, Mazor T, Olshen AB, Geng H, Gelston LC, Akutagawa J, Lipka DB, Plass C, Flotho C, Chehab FF, Braun BS, Costello JF, Loh ML. PMID: 29259179; PMCID: PMC5736624.
      View in: PubMed   Mentions: 32     Fields:    Translation:HumansCellsCTClinical Trials
    14. PATH-08. THE PROGNOSTIC VALUE OF A NOVEL QUANTITATIVE MGMT PROMOTER METHYLATION SCORE FOR PATIENTS WITH GLIOBLASTOMA. Neuro-Oncology. 2017 Nov 6; 19(suppl_6):vi172-vi172. Ravi RA, Molinaro MA, Han HS, Chehab CF, Berger BM, Butowski BN. .
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    15. MPTH-25. THE PROGNOSTIC VALUE OF A NOVEL QUANTITATIVE MGMT PROMOTER METHYLATION SCORE FOR PATIENTS WITH GLIOBLASTOMA. Neuro-Oncology. 2016 Nov 1; 18(suppl_6):vi111-vi111. Han HS, Ravi RA, Molinaro MA, Taylor TJ, Clarke CJ, Oberheim-Bush ON, Chang CS, Berger BM, Chehab CF, Butowski BN. .
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    16. Novel TKI-resistant BCR-ABL1 gatekeeper residue mutations retain in vitro sensitivity to axitinib. Leukemia. 2016 06; 30(6):1405-9. Lasater EA, Massi ES, Stecula A, Politi J, Tan SK, Smith CC, Gunthorpe M, Holmes JP, Chehab F, Sali A, Shah NP. PMID: 26511402.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    17. First report of a deletion encompassing an entire exon in the homogentisate 1,2-dioxygenase gene causing alkaptonuria. PLoS One. 2014; 9(9):e106948. Zouheir Habbal M, Bou-Assi T, Zhu J, Owen R, Chehab FF. PMID: 25233259; PMCID: PMC4169433.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    18. 20 years of leptin: leptin and reproduction: past milestones, present undertakings, and future endeavors. J Endocrinol. 2014 Oct; 223(1):T37-48. Chehab FF. PMID: 25118207; PMCID: PMC4184910.
      View in: PubMed   Mentions: 29     Fields:    Translation:HumansAnimalsCells
    19. FoxO4 interacts with the sterol regulatory factor SREBP2 and the hypoxia inducible factor HIF2α at the CYP51 promoter. J Lipid Res. 2014 Mar; 55(3):431-42. Zhu J, Jiang X, Chehab FF. PMID: 24353279; PMCID: PMC3934728.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansAnimalsCells
    20. Duplication of C7orf58, WNT16 and FAM3C in an obese female with a t(7;22)(q32.1;q11.2) chromosomal translocation and clinical features resembling Coffin-Siris Syndrome. PLoS One. 2012; 7(12):e52353. Zhu J, Qiu J, Magrane G, Abedalthagafi M, Zanko A, Golabi M, Chehab FF. PMID: 23300646; PMCID: PMC3531478.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    21. Homozygous deletion of six olfactory receptor genes in a subset of individuals with Beta-thalassemia. PLoS One. 2011 Feb 24; 6(2):e17327. Van Ziffle J, Yang W, Chehab FF. PMID: 21390308; PMCID: PMC3044735.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    22. Chapter 36 Molecular Diagnostic Challenges of the Thalassemias. Molecular Diagnostics. 2010 Jan 1; 441-452. Chehab CF. .
      View in: Publisher Site   Mentions:
    23. Effects of FoxO4 overexpression on cholesterol biosynthesis, triacylglycerol accumulation, and glucose uptake. J Lipid Res. 2010 Jun; 51(6):1312-24. Zhu J, Mounzih K, Chehab EF, Mitro N, Saez E, Chehab FF. PMID: 20037138; PMCID: PMC3035494.
      View in: PubMed   Mentions: 12     Fields:    Translation:HumansCells
    24. Overexpression of the transcription factor Foxo4 is associated with rapid glucose clearance. Mol Cell Endocrinol. 2009 Aug 13; 307(1-2):217-23. Wang B, Zhu J, Mounzih K, Chehab EF, Ke Y, Chehab FF. PMID: 19410631.
      View in: PubMed   Mentions: 4     Fields:    Translation:AnimalsCells
    25. Obesity and lipodystrophy--where do the circles intersect? Endocrinology. 2008 Mar; 149(3):925-34. Chehab FF. PMID: 18202137; PMCID: PMC2275358.
      View in: PubMed   Mentions: 16     Fields:    Translation:HumansAnimals
    26. Deletion of the serotonin 2c receptor from transgenic mice overexpressing leptin does not affect their lipodystrophy but exacerbates their diet-induced obesity. Biochem Biophys Res Commun. 2006 Dec 15; 351(2):418-23. Wang B, Chehab FF. PMID: 17064660; PMCID: PMC1941709.
      View in: PubMed   Mentions: 11     Fields:    Translation:Animals
    27. Mosaicism for a full mutation, premutation, and deletion of the CGG repeats results in 22% FMRP and elevated FMR1 mRNA levels in a high-functioning fragile X male. Am J Med Genet A. 2006 Jul 01; 140(13):1463-71. Han XD, Powell BR, Phalin JL, Chehab FF. PMID: 16761284.
      View in: PubMed   Mentions: 21     Fields:    Translation:HumansCells
    28. The use of animal models to dissect the biology of leptin. Recent Prog Horm Res. 2004; 59:245-66. Chehab FF, Qiu J, Ogus S. PMID: 14749505.
      View in: PubMed   Mentions: 9     Fields:    Translation:Animals
    29. Overexpression of leptin in transgenic mice leads to decreased basal lipolysis, PKA activity, and perilipin levels. Biochem Biophys Res Commun. 2003 Dec 26; 312(4):1165-70. Ke Y, Qiu J, Ogus S, Shen WJ, Kraemer FB, Chehab FF. PMID: 14651995.
      View in: PubMed   Mentions: 3     Fields:    Translation:AnimalsCells
    30. Hyperleptinemia precipitates diet-induced obesity in transgenic mice overexpressing leptin. Endocrinology. 2003 Jul; 144(7):2865-9. Ogus S, Ke Y, Qiu J, Wang B, Chehab FF. PMID: 12810541.
      View in: PubMed   Mentions: 21     Fields:    Translation:AnimalsCells
    31. Genetics and Physiology Link Leptin to the Reproductive System. Leptin and Reproduction. 2003 Jan 1; 267-286. Chehab CF, Ewart-Toland EA, Mounzih MK, Qiu QJ, Ogus OS. .
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    32. Leptin-deficient mice backcrossed to the BALB/cJ genetic background have reduced adiposity, enhanced fertility, normal body temperature, and severe diabetes. Endocrinology. 2001 Aug; 142(8):3421-5. Qiu J, Ogus S, Mounzih K, Ewart-Toland A, Chehab FF. PMID: 11459786.
      View in: PubMed   Mentions: 29     Fields:    Translation:Animals
    33. Transgenic mice overexpressing leptin accumulate adipose mass at an older, but not younger, age. Endocrinology. 2001 Jan; 142(1):348-58. Qiu J, Ogus S, Lu R, Chehab FF. PMID: 11145598.
      View in: PubMed   Mentions: 21     Fields:    Translation:HumansAnimalsCells
    34. Leptin as a regulator of adipose mass and reproduction. Trends Pharmacol Sci. 2000 Aug; 21(8):309-14. Chehab FF. PMID: 10918637.
      View in: PubMed   Mentions: 17     Fields:    Translation:HumansAnimals
    35. Effect of the genetic background on the reproduction of leptin-deficient obese mice. Endocrinology. 1999 Feb; 140(2):732-8. Ewart-Toland A, Mounzih K, Qiu J, Chehab FF. PMID: 9927300.
      View in: PubMed   Mentions: 23     Fields:    Translation:Animals
    36. Leptin is not necessary for gestation and parturition but regulates maternal nutrition via a leptin resistance state. Endocrinology. 1998 Dec; 139(12):5259-62. Mounzih K, Qiu J, Ewart-Toland A, Chehab FF. PMID: 9832467.
      View in: PubMed   Mentions: 20     Fields:    Translation:HumansAnimals
    37. Cross-species characterization of the promoter region of the cystic fibrosis transmembrane conductance regulator gene reveals multiple levels of regulation. Biochem J. 1997 Nov 01; 327 ( Pt 3):651-62. Vuillaumier S, Dixmeras I, Messaï H, Lapouméroulie C, Lallemand D, Gekas J, Chehab FF, Perret C, Elion J, Denamur E. PMID: 9581539; PMCID: PMC1218840.
      View in: PubMed   Mentions: 16     Fields:    Translation:HumansAnimalsCells
    38. The reproductive side of leptin. Nat Med. 1997 Sep; 3(9):952-3. Chehab FF. PMID: 9288714.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    39. Molecular basis of asymptomatic beta-thalassemia major in an African American individual. Am J Med Genet. 1997 Mar 17; 69(2):196-9. Ballas SK, Cai SP, Gabuzda T, Chehab FF. PMID: 9056561.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    40. Leptin treatment rescues the sterility of genetically obese ob/ob males. Endocrinology. 1997 Mar; 138(3):1190-3. Mounzih K, Lu R, Chehab FF. PMID: 9048626.
      View in: PubMed   Mentions: 91     Fields:    Translation:Animals
    41. Early onset of reproductive function in normal female mice treated with leptin. Science. 1997 Jan 03; 275(5296):88-90. Chehab FF, Mounzih K, Lu R, Lim ME. PMID: 8974400.
      View in: PubMed   Mentions: 100     Fields:    Translation:Animals
    42. Trinucleotide repeats in the human genome: size distributions for all possible triplets and detection of expanded disease alleles in a group of Huntington disease individuals by the repeat expansion detection method. Hum Mol Genet. 1997 Jan; 6(1):77-83. Hofferbert S, Schanen NC, Chehab F, Francke U. PMID: 9002673.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    43. A broader role for leptin. Nat Med. 1996 Jul; 2(7):723-4. Chehab FF. PMID: 8673906.
      View in: PubMed   Mentions: 9     Fields:    Translation:Animals
    44. Correction of the sterility defect in homozygous obese female mice by treatment with the human recombinant leptin. Nat Genet. 1996 Mar; 12(3):318-20. Chehab FF, Lim ME, Lu R. PMID: 8589726.
      View in: PubMed   Mentions: 264     Fields:    Translation:HumansAnimalsCells
    45. Comparison of PCR detection of mecA with standard susceptibility testing methods to determine methicillin resistance in coagulase-negative staphylococci. J Clin Microbiol. 1996 Feb; 34(2):249-53. York MK, Gibbs L, Chehab F, Brooks GF. PMID: 8788995; PMCID: PMC228777.
      View in: PubMed   Mentions: 36     Fields:    Translation:HumansCells
    46. New frameshift mutation, insertion of A, at codon 95 of the beta-globin gene causes beta-thalassemia in two Vietnamese families. Hum Mutat. 1996; 8(3):293-4. Cai S, Chehab FF. PMID: 8889595.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    47. Detection of viral deoxyribonucleic acid in the amniotic fluid of low-risk pregnancies by polymerase chain reaction. Am J Obstet Gynecol. 1995 Oct; 173(4):1282-6. McLean LK, Chehab FF, Goldberg JD. PMID: 7485338.
      View in: PubMed   Mentions: 12     Fields:    Translation:HumansCells
    48. Methylation status of CpG sites in the mouse and human CFTR promoters. DNA Cell Biol. 1995 Sep; 14(9):811-5. Denamur E, Chehab FF. PMID: 7545404.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansAnimalsCells
    49. 10 Analysis of PCR Products by Covalent Reverse Dot Blot Hybridization. PCR Strategies. 1995 Jan 1; 130-139. Chehab CF, Wall WJ, Cai CS. .
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    50. A 31-mutation assay for cystic fibrosis testing in the clinical molecular diagnostics laboratory. Hum Mutat. 1995; 5(4):333-8. Wall J, Cai S, Chehab FF. PMID: 7627189.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    51. Uniparental isodisomy for paternal 7p and maternal 7q in a child with growth retardation. Am J Hum Genet. 1994 Aug; 55(2):253-65. Eggerding FA, Schonberg SA, Chehab FF, Norton ME, Cox VA, Epstein CJ. PMID: 7913578; PMCID: PMC1918369.
      View in: PubMed   Mentions: 15     Fields:    Translation:HumansCells
    52. Analysis of the mouse and rat CFTR promoter regions. Hum Mol Genet. 1994 Jul; 3(7):1089-94. Denamur E, Chehab FF. PMID: 7526924.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansAnimalsCells
    53. A new frameshift mutation, insertion of ATCT, at codon 48 in the beta-globin gene causes beta-thalassemia in an Indian proband. Hum Mutat. 1994; 3(4):397-8. Jain PK, Dozy AM, Verma IC, Chehab FF. PMID: 8081396.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    54. Analysis of gene sequences by hybridization of PCR-amplified DNA to covalently bound oligonucleotide probes. The reverse dot blot method. Methods Mol Biol. 1994; 28:225-36. Kawasaki ES, Chehab FF. PMID: 8118512.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    55. Reverse dot blot probes for the screening of beta-thalassemia mutations in Asians and American blacks. Hum Mutat. 1994; 3(1):59-63. Cai SP, Wall J, Kan YW, Chehab FF. PMID: 8118466.
      View in: PubMed   Mentions: 15     Fields:    Translation:HumansCells
    56. Rapid and simultaneous typing of hemoglobin S, hemoglobin C, and seven Mediterranean beta-thalassemia mutations by covalent reverse dot-blot analysis: application to prenatal diagnosis in Sicily. Blood. 1993 Jan 01; 81(1):239-42. Maggio A, Giambona A, Cai SP, Wall J, Kan YW, Chehab FF. PMID: 8417793.
      View in: PubMed   Mentions: 18     Fields:    Translation:HumansCells
    57. Molecular diagnostics: past, present, and future. Hum Mutat. 1993; 2(5):331-7. Chehab FF. PMID: 8257984.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    58. Detection of multiple cystic fibrosis mutations by reverse dot blot hybridization: a technology for carrier screening. Hum Genet. 1992 May; 89(2):163-8. Chehab FF, Wall J. PMID: 1587526.
      View in: PubMed   Mentions: 14     Fields:    Translation:HumansCells
    59. DNA amplification and reverse dot blot hybridization for detection and identification of mycobacteria to the species level in the clinical laboratory. J Clin Microbiol. 1992 May; 30(5):1220-4. Fiss EH, Chehab FF, Brooks GF. PMID: 1583123; PMCID: PMC265254.
      View in: PubMed   Mentions: 14     Fields:    Translation:HumansCells
    60. Amplification and detection of specific DNA sequences with fluorescent PCR primers: application to delta F508 mutation in cystic fibrosis. Methods Enzymol. 1992; 216:135-43. Chehab FF, Wall J, Kan YW. PMID: 1479898.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    61. A dimorphic 4-bp repeat in the cystic fibrosis gene is in absolute linkage disequilibrium with the delta F508 mutation: implications for prenatal diagnosis and mutation origin. Am J Hum Genet. 1991 Feb; 48(2):223-6. Chehab FF, Johnson J, Louie E, Goossens M, Kawasaki E, Erlich H. PMID: 1990833; PMCID: PMC1683013.
      View in: PubMed   Mentions: 19     Fields:    Translation:HumansCells
    62. Detection of the hemoglobin E mutation using the color complementation assay: application to complex genotyping. Blood. 1990 Aug 01; 76(3):619-23. Embury SH, Kropp GL, Stanton TS, Warren TC, Cornett PA, Chehab FF. PMID: 2378988.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    63. Detection of the hemoglobin E mutation using the color complementation assay: application to complex genotyping. Blood. 1990 Aug 1; 76(3):619-623. Embury ES, Kropp KG, Stanton ST, Warren WT, Cornett CP, Chehab CF. .
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    64. Detection of sickle cell anaemia mutation by colour DNA amplification. Lancet. 1990 Jan 06; 335(8680):15-7. Chehab FF, Kan YW. PMID: 1967329.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    65. The use of direct gene analysis to define beta-thalassemia. Ann N Y Acad Sci. 1990; 612:22-30. Dozy AM, Cai SP, Chehab F, Kan YW. PMID: 2291549.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    66. Detection of specific DNA sequences by fluorescence amplification: a color complementation assay. Proc Natl Acad Sci U S A. 1989 Dec; 86(23):9178-82. Chehab FF, Kan YW. PMID: 2594760; PMCID: PMC298457.
      View in: PubMed   Mentions: 23     Fields:    Translation:HumansCells
    67. Characterization of a spontaneous mutation in beta-thalassemia associated with advanced paternal age. Blood. 1989 Aug 01; 74(2):852-4. Chehab FF, Winterhalter KH, Kan YW. PMID: 2665856.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    68. Detection of cytomegalovirus infection in paraffin-embedded tissue specimens with the polymerase chain reaction. Mod Pathol. 1989 Mar; 2(2):75-8. Chehab FF, Xiao X, Kan YW, Yen TS. PMID: 2542930.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansCells
    69. Molecular basis of beta thalassemia in south China. Strategy for DNA analysis. Hum Genet. 1988 Jan; 78(1):37-40. Zhang JZ, Cai SP, He X, Lin HX, Lin HJ, Huang ZG, Chehab FF, Kan YW. PMID: 3338793.
      View in: PubMed   Mentions: 27     Fields:    Translation:Humans
    70. Human placental Na+,K+-ATPase alpha subunit: cDNA cloning, tissue expression, DNA polymorphism, and chromosomal localization. Proc Natl Acad Sci U S A. 1987 Nov; 84(22):7901-5. Chehab FF, Kan YW, Law ML, Hartz J, Kao FT, Blostein R. PMID: 2891135; PMCID: PMC299443.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansAnimalsCells
    71. Detection of sickle cell anaemia and thalassaemias. Nature. 1987 Sep 24-30; 329(6137):293-4. Chehab FF, Doherty M, Cai SP, Kan YW, Cooper S, Rubin EM. PMID: 3627274.
      View in: PubMed   Mentions: 46     Fields:    Translation:HumansCells
    72. The molecular basis of beta-thalassemia in Lebanon: application to prenatal diagnosis. Blood. 1987 Apr; 69(4):1141-5. Chehab FF, Der Kaloustian V, Khouri FP, Deeb SS, Kan YW. PMID: 3828533.
      View in: PubMed   Mentions: 17     Fields:    Translation:HumansCells
    73. Spontaneous mutation in beta-thalassaemia producing the same nucleotide substitution as that in a common hereditary form. Lancet. 1986 Jan 04; 1(8471):3-5. Chehab FF, Honig GR, Kan YW. PMID: 2867271.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansCells
    74. Genetic studies in a selected group of Lebanese beta-thalassemic patients. J Med Liban. 1986; 36(2):69-71. Khouri FP, Chehab FF, Deeb SS, Habbal ZM, Muallem HE. PMID: 3783632.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    75. Globin synthetic ratios in homozygous beta-thalassemia patients from Lebanon. Hemoglobin. 1984; 8(2):151-62. Chehab FF, Khouri FP, Deeb SS. PMID: 6206028.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
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