Hermann Lehmann

Hermann Lehmann's AcademicInfluence.com Rankings

Hermann Lehmann

Biology

#8469

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Pathology

#150

Historical Rank

Molecular Biology

#585

Historical Rank

Genetics

#623

Historical Rank

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Biology

Hermann Lehmann's Degrees

PhD Biochemistry University of Zurich
Doctorate Medicine University of Zurich

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Hermann Lehmann's Published Works

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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

Molecular Pathology of Human Haemoglobin (1968) (481)
On the evolution of myoglobin. (1978) (151)
Molecular Evolution of Myoglobin and the Fossil Record: a Phylogenetic Synthesis (1973) (147)
Haemoglobin GCopenhagen and haemoglobin JCambridge. Two new β-chain variants of haemoglobin A (1967) (136)
Haemoglobin Köln (β–98 Valine → Methionine): An Unstable Protein Causing Inclusion-Body Anaemia (1966) (133)
RAPID ESTIMATION (2 1/2 HOURS) OF GLYCOSYLATED HÆMOGLOBIN FOR ROUTINE PURPOSES (1977) (130)
Variations in the structure of human haemoglobin. With particular reference to the unstable haemoglobins. (1969) (127)
Molecular Pathology of Human Haemoglobin: Stereochemical Interpretation of Abnormal Oxygen Affinities (1971) (117)
Haemoglobin gene frequencies in the Jamaican population: a study in 100,000 newborns (1986) (117)
Haemoglobin Hammersmith (β 42 (CD1) Phe→Ser) (1967) (112)
Differences between α- and β-Chain Mutants of Human Haemoglobin and between α- and β-Thalassaemia. Possible Duplication of the α-Chain Gene* (1968) (99)
Two Haemoglobins Q, α74 (EF3) and α75 (EF4) Aspartic Acid→Histidine (1970) (86)
Abnormal Human Hæmoglobins: Hæmoglobin ‘Bart's’: a Fœtal Hæmoglobin without α-Chains (1959) (80)
Abnormal Haemoglobins and the Genetic Code (1965) (80)
A New Haemoglobin, D Ibadan (β-87 Threonine → Lysine), Producing No Sickle-Cell Haemoglobin D Disease with Haemoglobin S (1965) (79)
The unstable haemoglobin haemolytic anaemias. (1969) (70)
HÆMOGLOBIN TAK: A VARIANT WITH ADDITIONAL RESIDUES AT THE END OF THE β-CHAINS (1971) (68)
Hereditary Heinz-body Anaemia, Thrombocyttopenia, and Haemoglobinopathy (Hb Köln) in a Glasgow Family (1964) (65)
A New Hb Variant: Hb F Sardinia γ75 (e 19) Isoieucine→Threonine Found in a Family with Hb G Philadelphia, β-Chain Deficiency and a Lepore-Like Haemoglobin Indistinguishable from Hb A2 (1975) (65)
Chemical Heterogeneity of Hæmoglobin O (1962) (62)
Haemoglobin Genova: β28 (B10) Leucine→Proline (1967) (62)
Different types of alpha-thalassaemia and significance of haemoglobin Bart's in neonates. (1970) (62)
Haemoglobin Sydney: β67 (EII) Valine→ Alanine : an Emerging Pattern of Unstable Haemoglobins (1967) (59)
Abnormal Haem Binding and Globin SH Group Blockade in Unstable Haemoglobins (1968) (59)
A Haemoglobinopathy Involving Haemoglobin H and a New (Q) Haemoglobin (1958) (57)
α‐Thalassaemia as a Cause of Hydrops Foetalis (1962) (54)
Haemoglobin Korle-Bu (beta 73 aspartic acid replaced by asparagine) showing one of the two amino acid substitutions of haemoglobin C Harlem. (1968) (53)
Three Varieties of Human Hæmoglobin D (1958) (49)
Residue 122 of sperm whale and horse myoglobin (1974) (46)
Three Haemoglobins K: Woolwich, an Abnormal, Cameroon and Ibadan, Two Unusual Variants of Human Haemoglobin A (1965) (45)
Abnormal haemoglobins in Iran. Observation of a new variant--haemoglobin J Iran (alpha-2-beta-2 77 His--Asp). (1967) (44)
Hereditary non-spherocytic haemolytic anaemia with post-splenectomy inclusion bodies and pigmenturia caused by an unstable haemoglobin Santa Ana-beta-88 (F4) leucine--proline. (1968) (43)
Hemoglobin J Cape Town-alpha-2 92 arginine replaced by glutamine beta-2. (1966) (43)
Benign Obstetric History in Women with Sickle-cell Anaemia Associated with α-Thalassaemia (1972) (43)
Haemoglobin J Tongariki (alpha-115 alanine--aspartic acid): the first new haemoglobin variant found in a Pacific (Melanesian) population. (1967) (43)
Haemoglobin Torino – α43 (CDI) Phenylalanine→Valine (1968) (42)
The effect of magnesium on blood coagulation in human subjects. (1959) (42)
Haemoglobin titusville: α94 Asp → Asn: A new haemoglobin with a lowered affinity for oxygen (1975) (41)
Primary structure of human myoglobin. (1971) (41)
Public Health and Genetic Constitution of the San (“Bushmen”): Carbohydrate Metabolism and Acetylator Status of the! Kung of Tsumkwe in the North-western Kalahari* (1974) (41)
A New Hæmoglobin—Ja Oxford Found During a Survey of an English Population (1964) (40)
Haemoglobin A′2 : α2δ216 Glycine→Arginine (1966) (39)
Haemoglobins of Sheep (1966) (39)
An Unstable Haemoglobin with Reduced Oxygen Affinity: Haemoglobin Peterborough, (βiii (G13) Valine → Phenylalanine, its Interaction with Normal Haemoglobin and with Haemoglobin Lepore (1972) (39)
Synthesis of haemoglobin Lepore. (1972) (39)
Mild “Unstable Haemoglobin Haemolytic Anaemia” caused by Haemoglobin Shepherds Bush (B74 (E18) Gly→Asp) (1970) (38)
Sickling Phenomenon in Deer (1960) (38)
Molecular pathology of human haemoglobin. (1968) (38)
A NEW HEMOGLOBIN VARIANT RESEMBLING HEMOGLOBIN E: HEMOGLOBIN E SASKATOON-β22Glu→Lys (1967) (38)
Haemoglobin “Norfolk”: A New Haemoglobin Found in an English Family (1958) (36)
Two new pathological haemoglobins: Olmsted beta 141 (H19) Leu leads to Arg and Malmö beta 97 (FG4) His leads to Gln. (1970) (35)
The myoglobin of rodents:Lagostomus maximus (viscacha) andSpalax ehrenbergi (mole rat) (1984) (35)
OBSERVATIONS ON THE EFFECT OF MAGNESIUM ON BLOOD COAGULATION (1960) (35)
Haemoglobin P-Nilotic containing a - chain. (1973) (35)
Köln Haemoglobinopathy: FURTHER DATA AND A COMPARISON WITH OTHER HEREDITARY HEINZ BODY ANAEMIAS (1967) (35)
A New Haemoglobin in a Thai Family. A Case of Haemoglobin Siriraj-β Thalassaemia (1965) (35)
Haemoglobin D Punjab (D Los Angeles) (1974) (33)
Haemoglobin Buccureşti 42(CD1) Phe-Leu, a cause of unstable haemoglobin haemolytic anaemia. (1971) (33)
Familial Polycythaemia Caused by a New Haemoglobin Variant: Hb Heathrow, β 103 (G5) Phenylalanine Leucine (1973) (32)
Haemoglobin Rahere (beta Lys-Thr): A new high affinity haemoglobin associated with decreased 2, 3-diphosphoglycerate binding and relative polycythaemia. (1975) (31)
Hemoglobin Duarte: (α2β262(E6)Ala→Pro): A New Unstable Hemoglobin With Increased Oxygen Affinity (1974) (31)
Haemoglobin Koelliker: A New Acquired Haemoglobin Appearing after Severe Haemolysis: α2 minus 141 Arg β2 (1967) (30)
The myoglobin of primates. I. Hylobates agilis (gibbon). (1971) (30)
Haemoglobin Tak: a variant with additional residues at the end of the beta-chains. (1971) (30)
‘Multiple’ Hæmoglobins in the Horse (1958) (29)
Haemoglobin F Hull (gamma-121 glutamic acid--lysine), homologous with haemoglobins O Arab and O Indonesia. (1967) (29)
Haemoglobin Madrid beta 115 (G17) alanine--proline: an unstable variant associated with haemolytic anaemia. (1974) (28)
A new cause of haemolytic anaemia in the newborn. A description of an unstable fetal haemoglobin: F Poole, alpha2-G-gamma2 130 trptophan yeilds glycine. (1975) (28)
Haemoglobin O Arab in Sudanese (1966) (28)
Human embryonic haemoglobins including a comparison by homology of the human ζ and α chains (1975) (27)
HÆMOGLOBIN SOUTHAMPTON, β106 (G8) Leu →Pro: AN UNSTABLE VARIANT PRODUCING SEVERE HÆMOLYSIS (1972) (27)
Haemoglobin Osu-Christiansborg: a new beta-chain variant of haemoglobin A ( beta52 (D3) aspartic acid leads to asparagine) in combination with haemoglobin S. (1971) (27)
HÆmoglobin GAccra (1964) (27)
Haemoglobin F Texas I (α2γ25Glu→Lys): a Variant of Haemoglobin F (1967) (26)
Haemoglobin Dhofar--a new variant from Southern Arabia. (1968) (26)
The genetical interpretation of haemoglobin H disease. (1970) (26)
The myoglobin of primates. II. Pan Troglodytes (chimpanzee). (1972) (26)
Hb Helsinki: a Variant with a High Oxygen Affinity and a Substitution at a 2,3-DPG Binding Site (β82 [EF6] Lys→Met) (1976) (25)
Hæmoglobin E in Malaya (1956) (25)
A Ghanaian adult, homozygous for hereditary persistence of foetal haemoglobin and heterozygous for elliptocytosis. (1970) (25)
The amino acid sequence of human myoglobin and its minor fractions (1974) (24)
The myoglobin of primates. V. Prosimians: Galago crassicaudatus (thick-tailed galago) and Lepilemur mustelinus (sportive lemur). (1973) (24)
New Variant of Human Fœtal Hæmoglobin (1959) (24)
Synthesis of Hb Lepore ( 2 2 ): influence of and nucleotide sequence on synthesis of chain. (1972) (24)
Hemoglobin I in an American Negro family: structural and hematologic studies. (1966) (24)
Storage of Red Cells for Blood-grouping after Freezing in Liquid Nitrogen (1960) (24)
Haemoglobin Stanleyville II (α78 Asparagine→Lysine) (1968) (24)
The oxygen affinity of haemoglobin tak, a variant with an elongated β chain (1975) (24)
Haemoglobin F Texas II (α2γ26 Glu→Lys), the Second of the Haemoglobin F Texas Variants (1968) (24)
Abnormal haemoglobins in zambia. A new haemoglobin zambia α60 (E9) lysine→Asparagine (1969) (23)
Myoglobin of the orangutan as a phylogenetic enigma (1976) (23)
The Second Variant of Human Myoglobin; 138 (H16) Arginine → Glutamine (1971) (23)
HEMOGLOBIN G SASKATOON: β22Glu → Ala (1967) (23)
A New Haemoglobin, J Toronto (α5 Alanine → Aspartic Acid) (1965) (23)
The myoglobin of primates. 3. Cercopithecidae (Old World monkeys): Papio anubis (olive baboon) and Macaca fascicularis (=irus, crab-eating monkey). (1972) (22)
XI. The hereditary blood factors of the Kurds of Iran. (1973) (22)
The First Observation of an Abnormal Haemoglobin in a Jewish Family: Haemoglobin Beilinson (1963) (22)
New Human Haemoglobin Variant from Southern Arabia: G-Audhali (α23(B4) Glutamic Acid→Valine) and the Variability of B4 in Human Haemoglobin (1968) (22)
The River Niger as a Barrier in the Spread Eastwards of Hæmoglobin C: a Survey of Hæmoglobins in the Ibo (1959) (21)
New unstable haemoglobin (Hb Moscva, β24 (B4) Gly→Asp) found in the USSR (1974) (21)
Abnormal Human Myoglobin: 53 (D4) Glutamic Acid→Lysine (1969) (21)
Haemoglobin Denmark Hill 95 (G2) Pro-Ala, a variant with unusual electrophoretic and oxygen-binding properties. (1972) (20)
Haemoglobin J Sardegna: α50 (CD 8) Histidine → Aspartic Acid (1968) (20)
Hemoglobin Manitoba: α102(G9) serine replaced by arginine (1970) (20)
The myoglobin of primates. 4. New World monkeys: Cebidae: (1) Saimiri sciureus (squirrel monkey); (2) Lagothrix lagothricha (Humboldt's woolly monkey). Callitrichidae: Callithrix jacchus (common marmoset). (1973) (20)
Hemoglobin Etobicoke: α84(F5) serine replaced by arginine. (1969) (20)
Hemoglobin Riyadh-α2β2 (120 [GH3] Lys→Asn): A New Variant Found in Association with α-Thalassemia and Iron Deficiency (1976) (19)
Observations on haemoglobin P (Congo type). (1970) (19)
New Unstable Haemoglobin Borås: β88 (F4) Leucine→Arginine (1969) (19)
MAPPING OF ANTIGENIC SITES ON HUMAN HAEMOGLOBIN BY MEANS OF MONOCLONAL ANTIBODIES AND HAEMOGLOBIN VARIANTS (1981) (19)
Haemoglobin Titusville: alpha94 Asp replaced by Asn. A new haemoglobin with a lowered affinity for oxygen. (1975) (19)
Hæmoglobin P in a Family in the Belgian Congo (1959) (19)
Haemoglobin "Bart's': a foetal haemoglobin without alpha-chains. (1959) (19)
Haemoglobin G Copenhagen and haemoglobin J Cambridge. Two new beta-chain variants of haemoglobin A. (1967) (19)
DUPLICATION OF ALPHA-THALASSÆMIA GENE IN THREE GREEK FAMILIES WITH HÆMOGLOBIN H DISEASE (1970) (19)
Blood Groups and Enzymes of Human Red Cells After a Year's Storage in Liquid Nitrogen (1962) (18)
TWO UNRELATED PATIENTS WITH CONGENITAL CYANOSIS DUE TO HAEMOGLOBINOPATHY M. (1964) (18)
Homozygous Sickle-cell Anaemia Arising from two Different Haemoglobins S (1964) (18)
Sickle-Cell Anæmia and Sickle-Cell Trait as Homo- and Heterozygous Gene-Combinations (1951) (17)
Is haemoglobin G Philadelphia linked to -thalassaemia? (1971) (17)
The ξ‐chain, an α‐like chain of human embryonic haemoglobin (1974) (16)
Haemoglobin L Persian Gulf: α57 (E6) Glycine → Arginine (1969) (16)
The third variant of human myoglobin showing an unusual amino acid substitution: 138(H16)arginine--tryptophan. (1971) (16)
Hemoglobin Setif (α94 (G1) ASP → TYR) in Iran a Report of 9 Cases (1977) (16)
Hemoglobin winnipeg: Ά275 Asp → Tyr β2 (1973) (16)
Haemoglobin J Cape Town—α2 92 Arginine→Glutamine β2 (1966) (16)
Haemoglobin D-beta Los Angeles (D Punjab, alpha-2-beta-2 121 Glu NH2) in a Thai family. (1968) (16)
Hb K Woolwich the cause of a thalassaemia (1974) (16)
The primary structure of the myoglobin of rabbit (Oryctolagus cuniculus) (1976) (15)
Haemoglobin J Rajappen; 90 (FG2) Lys leads to Thr. (1971) (15)
Haemoglobin Nottingham, Beta FG 5 (98) Valgly: A New Unstable Haemoglobin Producing Severe Haemolysis (1973) (15)
The Clinical and Haematological Findings in Children Inheriting Two Types of Thalassaemia: High‐A2 Type β‐Thalassaemia, and High‐F Type or δβ‐Thalassaemia (1973) (15)
Haemoglobin F Malaysia: α2γ2 1 (NA1) Glycine→Cysteine; 136 Glycine (1974) (15)
Malignant hyperthermia in pigs: A search for abnormalities in Ca2+ binding proteins (1983) (15)
A human myoglobin variant 133 (H-10)lysine--asparagine. (1971) (15)
Hb altdorf α2β2 135 (H13) Ala → Pro: A new electrophoretically silent unstable haemoglobin variant from switzerland (1976) (14)
Structure of haemoglobin Wien beta 130 (H8) tyrosine-aspartic acid: an unstable haemoglobin variant. (1974) (14)
A new haemoglobin J from Turkey ‐ HB Ankara (β 10 (A7) Ala → Asp). (1974) (14)
A survey for haemoglobin variants, thalassaemia and glucose-6-phosphate dehydrogenase deficiency in northern Ghana. (1968) (14)
A new abnormal hemoglobin O Padova, alpha 30 (B11) Glu -- Lys, and a dyserythropoietic anemia with erythroblastic multinuclearity coexisting in the same patient. (1974) (14)
Haemoglobin Korle-Bu (β73 aspartic acid→asparagine) showing one of the two amino acid substitutions of haemoglobin C Harlem. (1968) (14)
Further characterisation of haemoglobin F Texas I: γ5 glutamic acid → lysine; γ136 alanine (1972) (14)
Zinc acetate as a precipitant of unstable haemoglobins. (1981) (14)
Abnormal haemoglobins in Iran. Observation of a new variant haemoglobin J. Iran (α2 β2 77 His -> Asp). (1967) (14)
Human skeletal muscle proteins (1976) (14)
Haemoglobin handsworth α 18 (A16) glycine → arginine (1977) (14)
The myoglobin of primates. VI. Tupaia glis belangeri (common treeshrew). (1974) (14)
An Abnormal Hæmoglobin in a Chinese: Hæmoglobin G (1958) (14)
The myoglobin of primates. VIII. Nycticebus coucang (slow loris). (1976) (13)
A New Haemoglobin Variant Haemoglobin J Birmingham a 120 (H3) Ala → Glu (1974) (13)
β-THALASSÆMIA, GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY, AND HÆMOGLOBIN D-PUNJAB IN PATHANS (1968) (13)
N‐terminal chain elongation as evidence for duplication of myoglobin in three South American Monkeys (1973) (13)
Absence of the Sickle Cell Trait in Seventy-two Australian Aboriginals (1953) (13)
Haemoglobin J Paris in the south of Portugal (Algarve). (1968) (13)
Haemoglobin M Saskatoon with slight constant haemolysis, markedly increased by sulphonamides. (2009) (13)
Evolution of Myoglobin Amino Acid Sequences in Primates and Other Vertebrates (1976) (13)
Haemoglobin North Shore‐Caracas β134 (H12) valine → glutamic acid (1977) (13)
The myoglobin of the fruit-bat (Rousettus aegyptiacus). (1977) (13)
Haemoglobin J Nyanza: 21 (B2) Ala-Asp. (1973) (13)
A new unstable haemoglobin: Hb Buenos Aires, beta 85 (F1) Phe leads to Ser. (1973) (13)
Sickle Cell Haemoglobin D Punjab Disease: S from Ghana and D from England (1967) (12)
Haemoglobin G norfolk: α 85 (F6) Asp → Asn (1975) (12)
Haemoglobin Osu-Christiansborg: a new β-chain variant of haemoglobin A (β52 (D3) aspartic acid → asparagine) in combination with haemoglobin S. (1971) (12)
Compensation of chain synthesis by the single chain gene in Hb Lepore trait. (1972) (12)
Duplication of alpha-thalassaemia gene in three Greek families with haemoglobin H disease. (1970) (12)
High Resolution Nuclear Magnetic Resonance Studies of Haemoglobin J Capetown (1970) (12)
Comparison of the myoglobin of the zebra (Equus burchelli) with that of the horse (Equus caballus). (1975) (12)
Blood groups and enzymes of human red cells after five years' storage in liquid nitrogen. (1962) (12)
Incidence of Pseudocholinesterase Variants in Australian Aborigines (1963) (12)
Hemoglobin S-G (S-D) syndrome. (1974) (11)
The myoglobin of the killer whale (Orcinus orca). (1977) (11)
Haemoglobin Warwickshire (beta 5 [A2] Pro----Arg). A possible 'fine tuning' of 2,3-DPG affinity by beta 5 Pro. (1984) (11)
The first observation of Hb D Punjab beta zero thalassaemia in an English family with 22 cases of unsuspected beta zero thalassaemia minor among its members. (1985) (11)
Sedimentation Characteristics of the γ-Chain Hæmoglobin (Hæmoglobin ‘Bart's’) (1960) (11)
Hereditary persistence of fetal hemoglobin, beta thalassemia, and the hemoglobin delta-beta locus: further family data and genetic interpretations. (1975) (11)
Structure and function of a new hemoglobin variant, Hb meilahti (alpha 2 beta 2 36(C2)Pro----Thr), characterized by mass spectrometry. (1987) (11)
Beta-Thalassaemia and Some Rare Haemoglobin Variants in the Highlands of Scotland (1973) (11)
Haemoglobin Hammersmith (beta-42 (CDI) Phe replaced by ser). (1967) (11)
Further Investigations of the γ-Chain in a Ghanaian Adult, Homozygous for Hereditary Persistence of Fetal Haemoglobin (1975) (10)
Haemoglobin Belfast 15 (A12) Tryptophan→Arginine: A New Unstable Haemoglobin Variant (1974) (10)
Haemoglobin J Baltimore in a Kent Family (1964) (10)
Globin synthesis in subjects doubly heterozygous for hemoglobin G-Philadelphia and hemoglobin S or C. (1975) (10)
Interaction between Iron Deficiency and α-Thalassaemia: the in vitro Effect of Haemin on α-Chain Synthesis (1978) (10)
Haemolytic Anaemia due to Haemoglobin Torino (1970) (10)
The myoglobin of the Cape hunting dog (Lycaon pictus). (1976) (10)
Unstable haemoglobin Köln disease in members of a Malay family. (1972) (10)
Absence of Abnormal Hæmoglobins in some Australian Aboriginals (1956) (10)
Haemoglobin Ottawa: a215 (Al3) Gly ? Arg 2 (1974) (10)
A new haemoglobin J-habana-α71(E20) alanine→glutamic acid (1974) (10)
Blood Groups of Human Red Cells after Two Years' Storage in Liquid Nitrogen (1964) (10)
Blood Groups and Enzymes of Human Red Cells after Two Years' Storage in Liquid Nitrogen (1963) (10)
Structure and Function of Haemoglobin Tacoma (β30 Arg→Ser) Found in a Second Family (1974) (10)
Unstable haemoglobin disease caused by Hb Santa Ana- 88 (F4) Leu leads to Pro. (1970) (10)
Hemoglobin Broussais: a 90 Lys?Asn (1970) (10)
The occurrence of hemoglobins E and E-Saskatoon in central Canada. (1973) (10)
Haemoglobin·Indonesia (α 116 Glu → Lys) in an Italian Family (1970) (10)
Erythraemia due to Haemoglobin San Diego (1975) (10)
A Hb J cape town homozygote — association of Hb J cape town and alpha‐thalassaemia (1978) (9)
The γ chain of the lamb (1976) (9)
The oxygen affinity of haemoglobin Tak, a variant with an elongated beta chain. (1975) (9)
The primary structure of the myoglobin of Didelphis marsupialis (Virginia opossum). (1975) (9)
The amino acid substitution in Hb olmsted: β141 (H19) leucine → arginine (1975) (9)
An abnormal haemoglobin in a Chinese: haemoglobin G. (1958) (9)
Hb shaare zedek (α56 E5 Lys → Glu) (1980) (9)
Investigation of malignant hyperthermia: analysis of skeletal muscle proteins from normal and halothane sensitive pigs by two dimensional gel electrophoresis. (1983) (9)
Identification of haemoglobin C Georgetown. (1972) (9)
Hæmogram, Serum Protein and Plasma Volume of Healthy, Well nourished East Africans in Uganda (1949) (9)
Hb Heathrow: beta G5 103 phenylalanine-leucine: a new high affinity haemoglobin. (1973) (9)
Chemical heterogeneity of haemoglobin O. (1962) (9)
Human haemoglobins and haemoglobinopathies in Arabia: Hb O Arab in Saudi Arabia. (1980) (9)
Further characterization of haemoglobin F hull γ121 glutamic acid → lysine; γ136 alanine (1973) (9)
Hb Serbia (α112 (G19) His→Arg), a new haemoglobin variant from Yugoslavia (1975) (9)
Myoglobin in Primary Muscular Disease: I. Duchenne Muscular Dystrophy: and: II. Muscular Dystrophy of Distal Type (1973) (9)
COMPARATIVE STRUCTURE OF MYOGLOBIN: PRIMATES AND TREE‐SHREW (1974) (8)
Haemoglobin ferndown (α6 [A4] aspartic acid → valine) (1981) (8)
Urinary amino acids and calcium in relation to renal stones and renal damage. (1962) (8)
Hyperlipoproteinaemia classification: the optimum routine electrophoretic system and its relevance to treatment. (1972) (8)
The myoglobin of an echidna (Tachyglossus aculeatus aculeatus). (1978) (8)
Structural identification of haemoglobin F Kuala Lumpur: α2γ2 22(B4) Asp → Gly; 136 Ala (1973) (8)
Comparison of the myoglobin of the bat-eared fox (Otocyon megalotis) with that of the domestic dog (Canis familiaris). (1976) (8)
Homozygous haemoglobin D Punjab. (1975) (8)
Haemoglobin M Hyde Park: a hereditary methaemoglobinaemia in a Caucasian child. (1968) (8)
Two haemoglobins Q, alpha-74 (EF3) and alpha-75 (EF4) aspartic acid to histidine. (1970) (7)
The myoglobin of primates. VII. Perodicticus potto edwarsi (potto). (1975) (7)
Haemoglobin Stanleyville II (alpha asparagine replaced by lysine). (1968) (7)
The primary structure of the myoglobin of the insectivore Erinaceus europaeus (common European hedgehog). (1975) (7)
The myoglobin of primates. VIII. Gorilla gorilla beringei (eastern highland gorilla). (1975) (7)
Absence of the Diego Blood Group and Abnormal Hæmoglobins in 92 Maoris (1958) (7)
Beta-thalassaemia, glucose-6-phosphate-dehydrogenase deficiency, and haemoglobin D-Punjab in Pathans. (1968) (7)
Haemoglobin Hijiyama: a haemoglobin variant found in connection with glycosylated haemoglobin estimation in a Finnish diabetic boy. (1982) (7)
Haemoglobin K Woolwich (α2β2132 Lysine → Glutamine) in Ghana (1971) (7)
Haemoglobin LeporeBaltimore in a Spanish family. (1983) (6)
Haemoglobin O Arab in Egypt and Aden: possible errors resulting from the use of haemoglobin variants as genetic markers in population surveys. (1967) (6)
Haemoglobin Stanleyville II (α 78 [EF 7] Asn → Lys) Found in France (1975) (6)
Differences between alpha- and beta-chain mutants of human haemoglobin and between alpha- and beta-thalassaemia. Possible duplication of the alpha-chain gene. (1968) (6)
Congenital Heinz body haemolytic anaemia due to haemoglobin Perth in a Nama child seemingly aggravated by the high nitrate content of the water supply. (1977) (6)
Haemoglobin Warwickshire (β5 [A2] Pro → Arg) (1984) (6)
Hb F Kingston (Gγ55 [D6] Met→Arg) (1982) (6)
HAEMOGLOBIN KÖLN IN A JEWISH FAMILY (1972) (6)
Haemoglobin G-Szuhu, beta80 Asn-Lys, in the homozygous state in a patient with abetalipoproteinaemia. (1975) (6)
The detection of abnormal and foetal haemoglobin in blood stains. (1963) (6)
Hemoglobin UBE-2 (α68 ASN→ASP) Observed in a Turkish Family (1984) (6)
Is haemoglobin Gα Philadelphia linked to α-thalassaemia? (1976) (6)
Blood Markers (1969) (5)
Hemoglobin Hofu Associated with β°-Thalassemia (1985) (5)
A new hemoglobin variant resembling hemoglobin E. Hemoglobin E Saskatoon: beta-22 Glu replaced by Lys. (1967) (5)
An unstable haemoglobin with reduced oxygen affinity: haemoglobin Peterborough, 3 (GI3) Valine lead to Phenylalanine, its interaction with normal haemoglobin and with haemoglobin Lepore. (1972) (5)
New variant of human foetal haemoglobin. (1959) (5)
alpha-Thalasaemia as a cause of hydrops foetalis. (1962) (5)
The myoglobin of the Cape fox (Vulpes chama). (1977) (5)
The myoglobin of primates: Symphalangus syndactylus (SIAMANG) (1977) (5)
The Precipitation of Hemoglobin by Zinc: Its Application to the Isolation of a Minor Hemoglobin Fraction (Hbβ2 δ16 Gly → Arg) from Lysed whole Blood (1982) (5)
Hemoglobin Leiden [β6 or 7 (A3 or A4) GLU → 0] in a Yugoslavian Woman Arisen by a New Mutation (1983) (5)
The Absence of Haemoglobin C in 104 East Africans living in Dar es Salaam. (1955) (5)
Hemoglobin Duarte: (alpha2beta2 62(E6)Ala leads to Pro): a new unstable hemoglobin with increased oxygen affinity. (1974) (5)
Paradoxical Effect of Magnesium Ions on Blood Coagulation (1960) (5)
Sickle cell-Hb Lepore Boston syndrome. Uncommon differential diagnosis to homozygous sickle cell disease. (1982) (4)
Haemoglobin D Ouled Rabah (beta 19[Bl] asn leads to lys) in a Tuareg tribe of the Southern Sahara. (1977) (4)
[Hemoglobin A2 in the black populations of West Africa. 1st results of a study at Senegal]. (1974) (4)
THE SECOND OBSERVATION OF HAEMOGLOBIN NORFOLK OCCURRING IN AN ITALIAN FAMILY TOGETHER WITH BETA–THALASSAEMIA (1967) (4)
Hb Shaare Zedek (alpha 56 E5 Lys leads to Glu). (1980) (4)
TREATMENT OF SICKLE‐CELL DISEASE (1974) (4)
Twelve families with Hb 0 Arab in the Burgas district of Bulgaria observations on sixteen examples of Hb 0 β° thalassaemia (2004) (4)
HAEMOGLOBIN J BALTIMORE INTERACTING WITH BETA‐THALASSAEMIA IN AN AUSTRALIAN FAMILY (1967) (4)
Haemoglobin A2: alpha-2-delta-2-16 glycine--arginine. (1966) (4)
Haemoglobin A-2-NYU in a London population. (1975) (4)
Liquid nitrogen storage of haemoglobin variants (1964) (4)
Haemoglobin Torino--alpha-43 (CD1) phenylalanine replaced by valine. (1968) (4)
Sedimentation characteristics of the gamma-chain haemoglobin (haemoglobin Bart's). (1960) (4)
Man's Haemoglobin (2005) (4)
A new Hb variant: Hb F Sardinia gamma75(E19) isoleucine leads to threonine found in a family with Hb G Philadelphia, beta-chain deficiency and a Lepore-like haemoglobin indistinguishable from Hb A2. (1975) (4)
Haemoglobin Stanleyville II (alpha75 [EF 7] Asn yeilds Lys) found in France. (1975) (4)
Haemoglobin D ΒPunjab in an East Anglian Family (1965) (4)
[Two fast hemoglobins in Ivory-Coast: Hb K Woolwich and a new hemoglobin Hb J Abidjan (alpha-51 Gly-Asp)]. (1972) (3)
215. Possible Anthropological Significance of Haemoglobins O and O (1962) (3)
The occurrence of Hb E Saskatoon in Scotland (1976) (3)
Haemoglobin Southampton, 106 (G8) Leu leads to pro: an unstable variant producing severe haemolysis. (1972) (3)
Incidence of Hæmoglobin C in the ‘Coloured’ Population of Cape Town (1955) (3)
Haemoglobin Norfolk in Nepali Gorkhas (1975) (3)
Hemoglobin O Arabia. Considerations on the first nine cases discovered in Romania. (1975) (3)
Secretion of Pepsin in Achlorhydric Human Subjects after Injection of Histamine (1946) (3)
Haemoglobin K Woolwich: a study of the family of a homozygote. (1980) (3)
Hemoglobin Winnipeg: alpha2 75 Asp leads to Tyr beta2. (1973) (3)
Haemoglobin coventry (β 141 deleted) in iran (1978) (3)
Hb Helsinki: a variant with a high oxygen affinity and a substitution at a 2,3-DPG binding site (beta82[EF6] Lys replaced by Met). (1976) (3)
A new haemoglobin: Hb J Sardegna (alpha50 histidine--aspartic acid). (1969) (3)
Haemoglobin sydney: Beta-67 (E11) valine modified to alanine: an emerging pattern of unstable haemoglobins. (1967) (3)
The γ-Chain in a Ghanaian Adult, Homozygous for Hereditary Persistence of Fetal Haemoglobin (1974) (3)
Haemoglobin Handsworth alpha 18 (A16) glycine leads to arginne. (1977) (3)
Haemoglobin Shepherds Bush (beta 74 [E 18] Gly leads to Asp) in an Italian family. (1977) (3)
Effect of an Enzyme from Kidney on the Solubility of Calcium Phosphate (1942) (3)
Haemoglobin Genova: beta-28 (B10) leucine replaced by proline. (1967) (3)
Haemoglobin K Woolwich (alpha 2, beta 2 132 lysine leads to glutamine) in Ghana. (1971) (3)
Hemoglobin Riyadh--alpha2beta2 (120(GH3)Lys replaced by Asn). A new variant found in association with alpha-thalassemia and iron deficiency. (1976) (3)
Multiple haemoglobins in the horse. (1958) (3)
Haemoglobin G Norfolk: alpha 85 (F6) Asp leads to Asn. (1975) (3)
Familial polycythaemia caused by a new haemoglobin variant: Hb Heathrow, beta 103 (G5) phenylalanine leads to leucine. (1973) (3)
Haemoglobin Lepore Boston in a Spanish family. (1976) (3)
[Instable hemoglobin during hemolytic anemia with erythrocytic inclusions and black urine. Hemoglobin found in Lille, analogous to Santa Ana beta 88 (F4) hemoglobin leucine-proline]. (1970) (3)
Double heterozygosity for two unstable haemoglobins: Hb Sydney (beta67[E11] Val leads to Ala) and Hb Coventry (beta141[H19] Leu deleted). (1978) (2)
Adrenaline Treatment in Vitro and Liver Glycogen (1941) (2)
Hemoglobin Setif (alpha94 (G1) Asp replaced by Tyr) in Iram. A report of 9 cases. (1977) (2)
The Unstable Hb Genova (β28Leu→Pro) in an East African Family (1979) (2)
Urinary excretion of acid muco-polysaccharide in sibs with Morquio's syndrome and Reilly's granules in leucocytes. (1967) (2)
Hemoglobin J Toronto: α25Ala→Aspβ2 (1971) (2)
The second variant of human myoglobin; 138(H16) arginine leads to glutamine. (1971) (2)
Haemoglobin F Texas I(alpha-2,gamma-2-5glu-lys): a variant of haemoglobin F. (1967) (2)
Haemoglobin hasharon (2004) (2)
Haemoglobin Sogn (β14 Arginine) A New Haemoglobin Variant (2009) (2)
Action of Insulin in Cell-free Extracts (1938) (2)
Structure and function of haemoglobin Tacoma (beta 30 Arg yields Ser) found in a second family. (1974) (2)
HÆmoglobin D Punjab in a European Family in Australia (1973) (2)
Residues 124 and 125 (H2 and H3) of the human haemoglobin delta-chain. (1976) (2)
[Hemoglobin Stanleyville II and mucoviscidosis in an Alsatian family]. (1975) (2)
I Haemoglobin J Tongariki ( a II Alanine-- Aspartic Acid ) : the first new haemoglobin variant found in a Pacific ( Melanesian ) population (2)
Myoglobin variants. (1970) (2)
Hb Altdorf alpha2beta2 135 (H13) Ala leads to Pro: a new electrophoretically silent unstable haemoglobin variant from Switzerland. (1976) (2)
Haemoglobin North Shore-Caracas beta 134 (H12) valine replaced by glutamic acid. (1977) (2)
Hemoglobin Etobicoke: alpha-84(F5) serine replaced by arginine. (1969) (2)
A NEW HAEMOGLOBIN IN A THAI FAMILY. A CASE OF HAEMOGLOBIN SIRIRAJ-BETA THALASSAEMIA. (1965) (2)
A second family with hemoglobin M Saskatoon in Saskatchewan. (1974) (2)
The oxygen affinity of haemoglobin St. Luke's (1974) (2)
Sickle cell anemia 35 years ago: reminiscence of early African studies. (1984) (2)
The gamma-chain in a Ghanaian adult, homozygous for hereditary persistence of fetal haemoglobin. (1974) (1)
Haemoglobin Sogn (beta 14 arginine) a new haemoglobin variant. (1968) (1)
Haemoglobin F Texas II (alpha-2 gamma-2, 6 Glu-Lys), the second of the haemogloin F Texas variants. (1968) (1)
Haemoglobin O Arab, beta-thalassaemia and glucose-6-phosphate dehydrogenase deficiency in a Hungarian family. (1980) (1)
Distorted interviews in East Germany (1979) (1)
Abnormal haemoglobins in Zambia. A new haemoglobin Zambia alpha-60 (E9) lysine--asparagine. (1969) (1)
Haemoglobin L Persian Gulf: alpha-57 (E6) glycine leads to arginine. (1969) (1)
Red Cells after Three Years’ Storage in Liquid Nitrogen (1965) (1)
Myoglobin in Primary Muscular Disease (1)
Sickle-cell anaemia. (1969) (1)
Haemoglobin J Rovigo 53 alpha (E-2) aspartic acid alanin. (1980) (1)
Haemoglobin D Ouled Rabah ( p 19 [ B 1 ] Asn-- . Lys ) in a Tuareg tribe of the Southern Sahara (1)
Hemoglobin G Saskatoon: beta-22Glu--Ala. (1967) (1)
The zeta-chain, an alpha-like chain of human embryonic haemoglobin. (1974) (1)
The clinical and haematological findings in children inheriting two types of thalassaemia: high-A2, type beta-thalassaemia, and high-F type or delta beta-thalassaemia. (1973) (1)
Further characterisation of haemoglobin F Texas I 5 glutamic acid leads to lysine; 136 alanine. (1972) (1)
Hemoglobin Duarte: (a2fl?2?"#{176}?0):A New Unstable Hemoglobin With Increased Oxygen Affinity (1974) (1)
A new haemoglobin, J Toronto (alpha-5 alanine to aspartic acid). (1965) (1)
A new haemoglobin J from Turkey--Hb Ankara (beta10 (A7) Ala-Asp). (1974) (1)
Hemoglobin Ube-2 (alpha 68 Asn----Asp) observed in a Turkish family. (1984) (1)
Hemoglobin Leiden [beta 6 or 7 (A3 or A4) Glu leads to O] in a Yugoslavian woman arisen by a new mutation. (1983) (1)
The amino acid substitution in Hb Olmsted: beta141 (H19) leucine yields arginine. (1975) (1)
Red Cell Antigens and Enzymes after Storage at −196°C, −100°C and −78°C (1961) (1)
The gamma chain of the lamb. (1976) (1)
Homozygosity for the delta-chain variant haemoglobin A2' (HbB2) (delta 16 Gly----Arg). (1985) (1)
Selection at molecular level in mammalian myoglobins (1978) (1)
New unstable haemoglobin (Hb Moscva, beta24 (B4) Gly leads to Asp) found in the USSR. (1974) (1)
Beta-chain variants in Jamaican newborns. (1978) (1)
Interaction between iron deficiency and alpha-thalassaemia: the in vitro effect of haemin on alpha-chain synthesis. (1978) (1)
Haemoglobin Coventry (beta 141 deleted) in Iran. (1978) (1)
Haemoglobin Koelliker: a new acquired haemoglobin appearing after severe haemolysis: alpha-2 minus 141 Arg beta-2. (1967) (1)
[Study of an alpha J hemoglobin not previously described, in a French family]. (1966) (1)
Human embryonic haemoglobins including a comparison by homology of the human beta and alpha chains. (1975) (1)
Thawing of Blood Stored in Liquid Nitrogen by Means of Radio‐Frequency Heating (1962) (1)
Futher investigations of the gamma-chaina in a ghanaian adult, homozygous for hereditary perisitence of fetal haemoglobin. Isolation of gamma CB-3 peptides and Ggamma:Agamma ratio determination in human Hb E. (1975) (1)
Hemoglobin Hofu associated with beta 0-thalassemia. (1985) (0)
Haemoglobin F Malaysia: alpha 2, gamma 2 1(NA1) glycine--cysteine; 136 glycine. (1974) (0)
THALASSEMIA RESEARCH AND ABNORMAL HEMOGLOBINS (1969) (0)
[Interactions between Stanleyville 2 and S hemoglobins in a family from Zaire. Study of the Stanleyville 2-S hybrid (alpha 2-78Lys beta 2-6 Val)]. (1973) (0)
Hb Newcastle: beta92 (F8) His replaced by Pro. (1975) (0)
Hemoglobin J Toronto: alpha 2-5 Ala-Asp-beta 2. (1971) (0)
Haemoglobin O Indonesia (alpha 116 Glu leads to Lys) in an Italian family. (1970) (0)
Is haemoglobin G alpha Philadelphia linked to alpha-thalassaemia? (1971) (0)
Precipitation of hemoglobin by zinc: the detection and isolation of unstable hemoglobins and the concentration of dilute hemoglobin solutions. (1981) (0)
The Genetics of the Jews. By A.E. Mourant, Ada C. KopÉc and Kazimiera Domaniewska-Sobczak. Pp. viii + 122. (Oxford Iniversity Press, 1978.) Price £12.50 (1979) (0)
Twelve families with Hb O Arab in the Burgas district of Bulgaria. Observations on sixteen examples of Hb O Arab-beta (0) thalassaemia. (1975) (0)
A drug-induced haemolytic anaemia due to Hb Torino (alpha43(CD1)Phe replaced by Val). second finding in an Italian family. (1976) (0)
Hb F Kingston (G gamma 55 [D6] Met leads to Arg). (1982) (0)
A CASE OF HYPERTENSION WITH ISCHAEMIC KIDNEY DEMONSTRATED AT THE POSTGRADUATE MEDICAL SCHOOL OF LONDON. (1964) (0)
Interaction between beta-thalassaemia and Hb G Philadelphia associated with alpha-thalassaemia. (1979) (0)
Biochemical Genetics (1968) (0)
The precipitation of hemoglobin by zinc: its application to the isolation of a minor hemoglobin fraction (HbB2 delta 16 Gly replaced by Arg) from lysed whole blood. (1982) (0)
Serum Proteins (1967) (0)
A Drug-Induced Haemolytic Anaemia due to Hb Torino (α43(CDl)Phe→Val). Second Finding in an Italian Family (1976) (0)
Haemoglobin Belfast 15 (A12) tryptophan leading to arginine: a new unstable haemoglobin variant. (1974) (0)
Zinc acetate asaprecipitant ofunstable haemoglobins (1981) (0)
Haemoglobin Heathrow--a new high affinity haemoglobin. (1973) (0)
Nomenclature of the alpha-thalassaemias. (1984) (0)
Haemoglobin caribbean beta91 (F7) Leu replaced by Arg: a mildly haemoglobin with a low oxygen affinity. (1976) (0)
Haemoglobin A'2 in the black population of western Africa. (1974) (0)
Argentinian haematologist disappears (1978) (0)
Long-Term Preservation of Blood (1964) (0)
Interaction between haemoglobin Stanleyville II and haemoglobin S in a family from Zaire. Study of the hybrid Stanleyville II/S (α278lys β26val). (1973) (0)
CROSSINGS OVER VERSUS POINT MUTATIONS AS CAUSES OF HEMOGLOBIN VARIANTS AND POSSIBLY OF THALASSEMIAS (1978) (0)
[Hemoglobin O Arab--beta-thalassemia in a Bulgarian, a resident of Odessa]. (1978) (0)
INTERACTION OF BETA-THALASSAEMIA AND HEREDITARY PERSISTENCE OF FOETAL HAEMOGLOBIN. (1964) (0)
Structural identification of haemoglobin F Kuala Lumpur: alpha2 gamma2 22(B4)Asp leads to Gly; 136 Ala. (1973) (0)
Annotations (1889) (0)
A new causeofhaemolytic anaemia inthenewborn A description ofan unstable fetal haemoglobin: FPoole, 0120y2130 tryptophan -- glycine (1975) (0)
Interaction between β-Thalassaemia and Hb G Philadelphia Associated with α-Thalassaemia (1979) (0)
Enzyme Tests in Clinical Diagnosis (1963) (0)
Further characterization of haemoglobin F Hull 121 glutamic acid leads to lysine; 136 alanine. (1973) (0)
Hemoglobin Broussais: alpha-90 lys changed to asn. (1970) (0)
Haemoglobin Sherwood Forest beta104 (G6) Arg replaced by Thr. (1977) (0)
HAEMOGLOBIN GACCA. (1964) (0)
A new haemoglobin J-Habana-alpha71(E20) alanine leads to glutamic acid. (1974) (0)
Uncommon Differential Diagnosis to Homozygous Sickle Cell Disease (2016) (0)
Gamma Chain Variants in Jamaican Newborns (1976) (0)
TO-DAY'S DRUGS. TREATMENT OF ACUTE POISONING. I. (1964) (0)
Haemoglobin Ferndown (alpha 6 [A4] aspartic acid replaced by valine). (1981) (0)
Effect of Mono- and Divalent Salts on Red Blood Cells (1947) (0)
The unstable Hb Genova (beta 28Leu replaced by Pro) in an East African Family. Family study and the effect of splenectomy. (1979) (0)
Haemoglobin J Sardegna: alpha 50(CD 8) histidine -aspartic acid. (1968) (0)
Blood Enzymes (1964) (0)
d-fl Locus: Further Family Data and Genetic Interpretations (2006) (0)
New unstable haemoglobin borås: beta 88 (F4) leucine-arginine. (1969) (0)
Dystrophy of Distal Type Dystrophy : and : II . Muscular Disease : I . Duchenne Muscular Myoglobin in Primary Muscular (0)
NOMENCLATURE OF THE α-THALASSAEMIAS (1984) (0)

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