Samuel Rahbar
#1,677
Most Influential Person Now
Iranian biologist
Samuel Rahbar's AcademicInfluence.com Rankings
Samuel Rahbarbiology Degrees
Biology
#245
World Rank
#445
Historical Rank
Biotechnology
#35
World Rank
#36
Historical Rank
Molecular Biology
#2579
World Rank
#2620
Historical Rank
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Biology
Samuel Rahbar's Degrees
- Bachelors Biology University of Tehran
- Masters Biotechnology University of Tehran
- PhD Molecular Biology University of Tehran
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Why Is Samuel Rahbar Influential?
(Suggest an Edit or Addition)According to Wikipedia, Samuel Rahbar was an Iranian scientist who discovered the linkage between diabetes and HbA1C, a form of hemoglobin used primarily to identify plasma glucose concentration over time. Rahbar was born into a Jewish family in the Iranian city of Hamedan in 1929. He obtained his MD degree from the University of Tehran in 1953 and a PhD degree in immunology from the same university in 1963.
Samuel Rahbar's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- An abnormal hemoglobin in red cells of diabetics. (1968) (385)
- Novel inhibitors of advanced glycation endproducts. (2003) (364)
- Studies of an unusual hemoglobin in patients with diabetes mellitus. (1969) (356)
- Evidence that pioglitazone, metformin and pentoxifylline are inhibitors of glycation. (2000) (149)
- The Discovery of Glycated Hemoglobin: A Major Event in the Study of Nonenzymatic Chemistry in Biological Systems (2005) (117)
- Novel inhibitors of advanced glycation endproducts (part II). (2000) (103)
- Two Haemoglobins Q, α74 (EF3) and α75 (EF4) Aspartic Acid→Histidine (1970) (86)
- Anti-Inflammatory Effects of the Advanced Glycation End Product Inhibitor LR-90 in Human Monocytes (2007) (76)
- Novel inhibitors of glycation and AGE formation (2007) (70)
- LR-90 prevents methylglyoxal-induced oxidative stress and apoptosis in human endothelial cells (2014) (53)
- A new advanced glycation inhibitor, LR-90, prevents experimental diabetic retinopathy in rats (2008) (49)
- Advanced glycation end products of DNA: quantification of N2-(1-Carboxyethyl)-2'-deoxyguanosine in biological samples by liquid chromatography electrospray ionization tandem mass spectrometry. (2008) (48)
- Abnormal haemoglobins in Iran. Observation of a new variant--haemoglobin J Iran (alpha-2-beta-2 77 His--Asp). (1967) (44)
- Haemoglobin D Iran: β222 Glutamic Acid→Glutamine (B4) (1973) (42)
- Molecular analyses of beta-thalassemia in Iran. (1995) (37)
- Novel inhibitors of advanced glycation endproducts. (1999) (36)
- Small‑molecule COH-SR4 inhibits adipocyte differentiation via AMPK activation. (2013) (35)
- LR16, a compound with potent effects on the oxygen affinity of hemoglobin, on blood cholesterol, and on low density lipoprotein. (1988) (33)
- Reverse phase high-performance liquid chromatography and secondary ion mass spectrometry. A strategy for identification of ten human hemoglobin variants. (1986) (32)
- Rapid HPLC techniques for globin chain synthesis studies. (1989) (28)
- Discrimination among the transcripts of the allelic human β-globin genes βA, βS and βC using oligodeoxynucleotide hybridization probes (1986) (28)
- COH-SR4 Reduces Body Weight, Improves Glycemic Control and Prevents Hepatic Steatosis in High Fat Diet-Induced Obese Mice (2013) (26)
- Prevention of early renal disease, dyslipidaemia and lipid peroxidation in STZ‐diabetic rats by LR‐9 and LR‐74, novel AGE inhibitors (2005) (24)
- A new rapid method to detect inhibition of Amadori product generated by δ-gluconolactone (1999) (23)
- Novel dichlorophenyl urea compounds inhibit proliferation of human leukemia HL-60 cells by inducing cell cycle arrest, differentiation and apoptosis (2012) (22)
- A silent hemoglobin variant detected by HPLC: hemoglobin City of Hope beta 69 (E13) Gly----Ser. (1984) (20)
- Hemoglobin North Chicago (beta 36 [C2] proline----serine): a new high affinity hemoglobin. (1985) (18)
- Haemoglobin L Persian Gulf: α57 (E6) Glycine → Arginine (1969) (16)
- 1,3-Bis(3,5-dichlorophenyl) urea compound 'COH-SR4' inhibits proliferation and activates apoptosis in melanoma. (2012) (15)
- Effects of a new advanced glycation inhibitor, LR‐90, on mitigating arterial stiffening and improving arterial elasticity and compliance in a diabetic rat model: aortic impedance analysis (2014) (14)
- Hemoglobin H disease in two Iranian families. (1968) (14)
- Hemoglobin Hammersmith (beta 42 (CD1) Phe replaced by Ser) associated with severe hemolytic anemia. (1981) (14)
- Haemoglobin Hamadan: α2A β2 56 (D7) glycine → arginine (1975) (14)
- Abnormal haemoglobins in Iran. Observation of a new variant haemoglobin J. Iran (α2 β2 77 His -> Asp). (1967) (14)
- Hemoglobin Great Lakes (beta 68 [E12] leucine replaced by histidine): a new high-affinity hemoglobin (1981) (13)
- Renoprotective and Lipid‐Lowering Effects of LR Compounds, Novel Advanced Glycation End Product Inhibitors, in Streptozotocin‐Induced Diabetic Rats (2005) (13)
- Association of HB Hope [β 136(H14)GLY→ASP] and α-THALASSEMIA-2 (3.7 KB Deletion) Causing Severe Microcytic Anemia (1992) (12)
- Association of hemoglobin H disease with Hb J-Iran (beta 77 His----Asp): impact on subunit assembly. (1987) (12)
- Novel compound 1,3-bis (3,5-dichlorophenyl) urea inhibits lung cancer progression. (2013) (11)
- HB Watts [α74(EF3) OR α75(EF4)ASP→0]: A Shortened α Chain Variant Due to the Deletion of Three Nucleotides in Exon 2 of the α2-Globin Gene (1997) (11)
- Glycosylated minor C, D, and E hemoglobins. (1981) (11)
- Hemoglobin Lepore Boston in two Iranian families. (1974) (10)
- Hemoglobin Hammersmith as the Cause of Severe Hemolytic Anemia in a Chinese Girl (1986) (9)
- Haemoglobin Daneshgah-Tehran α2 72 (EF1) Histidine→Arginine βA2 (1973) (9)
- Indirect allosteric effects of a neutral mutation. Structure of deoxyhaemoglobin north Chicago (ProC2(36)beta----Ser). (1988) (9)
- Haemoglobin Arya: α247 (CD5), aspartic acid → asparagine (1975) (8)
- Haemoglobin D Iran: 2 22 glutamic acid leads to glutamine (B4). (1973) (7)
- Two haemoglobins Q, alpha-74 (EF3) and alpha-75 (EF4) aspartic acid to histidine. (1970) (7)
- Haemoglobin Avicenna (β47 (CD6) Asp → Ala). A new abnormal haemoglobin (1979) (7)
- Two new haemoglobins: haemoglobin Perspolis [a 64 (E13) AspåTyr] and haemoglobin J-Kurosh [a 19 (AB) AlaåAsp] (1976) (7)
- A new rapid method to detect inhibition of Amadori product generated by delta-gluconolactone. (1999) (6)
- Hemoglobin J Paris (α12 Alanine→Aspartic Acid) in Two Iranian Families (1972) (6)
- Further evidence for a post-translational phenomenon in the interaction of alpha-thalassemia with sickle cell trait. (1988) (6)
- Hemoglobin: Structure, function, evolution, and pathology. (1983) (5)
- Hemoglobin D Punjab in a Bulgarian Jewish family. (1969) (5)
- A Novel Initiation Codon Mutation (ATG→ATT) in a β-Thalassemia Patient (1993) (5)
- Iron overload in three generations of a family with hemoglobin Olympia. (1984) (5)
- Microcytosis in Hodgkin disease associated with unbalanced globin chain synthesis (1986) (5)
- A Second Case of Hemoglobin McKees Rocks (β145 Tyr → Term). A Variant with Premature Termination of the β-Chain (1983) (4)
- Haemoglobin Daneshgah-Tehran alpha2 72 (EPI) histidine--arginine betaA2. (1973) (4)
- A double heterozygous hemoglobin. Hemoglobin OIndonesia and hemoglobin DPunjab in an individual. (1975) (4)
- A case of homozygous haemoglobin Lepore Boston in Iran. (1975) (4)
- BETA THALASSEMIA ALLELS FOUND AMONG IRANIAN LIVING IN SOUTHERN CALIFORNIA (1990) (4)
- Splice junction [IVS-II-1 (G-->C)] thalassemia; a new mutation detected in an Iranian patient. (1993) (3)
- Mild sickle cell anemia associated with alpha globin mutant alpha Montgomery. (1989) (3)
- A second case of Hb hanamaki [α2139 (HC1) LYS→GLU β2] in an american family with erythrocytosis (1994) (3)
- Haemoglobin coventry (β 141 deleted) in iran (1978) (3)
- Hemoglobin Setif (alpha94 (G1) Asp replaced by Tyr) in Iram. A report of 9 cases. (1977) (2)
- Two new haemoglobins: haemoglobin Perspolis (alpha 64 (E13) Asp leads to Tyr) and haemoglobin J-Kurosh (alpha 19 (AB) Ala leads to Asp). (1976) (2)
- Discrimination among the transcripts of the allelic human beta-globin genes beta A, beta S and beta C using oligodeoxynucleotide hybridization probes. (1986) (2)
- Hemoglobin Osu-Christiansborg (beta52 (D3) Aspyield Asn) in an Iranian family. (1978) (2)
- Haplotype analysis of the human beta-globin gene complex using multiple locus specific oligonucleotide probes. (1988) (2)
- Association of Hb Hope [beta 136(H14)Gly----Asp] and alpha-thalassemia-2 (3.7 Kb deletion) causing severe microcytic anemia. (1992) (2)
- Hemoglobinopathies in the Los Angeles area. (1983) (2)
- Short Communications: Hemoglobin Osu-Christiansborg (β52 (D3) Asp→A5n) in an Iranian Family (2009) (2)
- Haemoglobin L Persian Gulf: alpha-57 (E6) glycine leads to arginine. (1969) (1)
- Two new haemoglobins: haemoglobin Perspolis [] and haemoglobin J-Kurosh [] (1976) (1)
- A second case of hemoglobin McKees Rocks (beta 145 Tyr leads to Term). A variant with premature termination of the beta-chain. (1983) (1)
- Haemoglobin Coventry (beta 141 deleted) in Iran. (1978) (1)
- Haemoglobin M Boston in an Iranian family. (1977) (1)
- A novel initiation codon mutation (ATG-->ATT) in a beta-thalassemia patient. (1993) (1)
- Thalassemia: Recent advances in detection and treatment (1984) (1)
- Protein Glycation and Diabetic Vascular Disease (1998) (1)
- Haemoglobin hamadan: alpha-2A beta-2 56 (D7) glycine yields arginine. (1975) (1)
- Abstract 2149: Novel compound 1, 3-bis (3, 5-dichlorophenyl) urea inhibits lung cancer progression (2014) (1)
- Haemoglobin Arya: alpha 2-47 (CD5), aspartic acid yields asparagine. (1975) (1)
- A New High-Affinity Hemoglobin (2017) (0)
- LR-90 prevents methylglyoxal-induced oxidative stress and apoptosis in human endothelial cells (2014) (0)
- Sickle cell disease. (1986) (0)
- A novel intrachromosomal rearrangement in the beta-globin gene found in an African-American family. (1995) (0)
- Haemoglobin O Indonesia (α116 Glutamic Acid → Lysine) in an Iranian Family (1973) (0)
- Haemoglobin Avicenna (beta 47 (CD6) Asp replaced by Ala). A new abnormal haemoglobin. (1979) (0)
- Abstract 5518: A novel 1,3-bis(3,5-dichlorophenyl) urea compound ‘COH-SR4’ for targeting melanoma. (2013) (0)
- A Novel Intrachromosomal Rearrangement in the β-Globin Gene Fd in An African-American Family (1995) (0)
- Hb Watts [alpha 74(EF3) or alpha 75(EF4)Asp-->0]: a shortened alpha chain variant due to the deletion of three nucleotides in exon 2 of the alpha 2-globin gene. (1997) (0)
- New inhibitors of the formation of advanced glycosylation (2002) (0)
- Hemoglobin Great Lakes (beta 68 [E12] leucine replaced by histidine): a new high-affinity hemoglobin. (1981) (0)
- New inhibitors of the formation of ages (advanced glycation endproducts) (2004) (0)
- Hemoglobin pasadena: Identification of the gene mutant by DNA analysis using synthetic DNA probes (1988) (0)
- A second case of Hb Hanamaki [alpha 2 139(HC1)Lys->Glu beta 2] in an American family with erythrocytosis. (1994) (0)
- Functional studies, anion-binding and effects of bezafibrate on three high affinity hemoglobin variants: Hb Olympia, Hb Great Lakes and Hb North Chicago. (1986) (0)
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