Citation Impact
Citing Papers
Hydrogen sulfide mediates the vasoactivity of garlic
2007 Standout
Evidence for an elevated frequency of in vivo somatic cell mutations in ataxia telangiectasia.
1989
Psychological Universals: What Are They and How Can We Know?
2005
Sequence and exon-intron organization of the DNA encoding the alpha I domain of human spectrin. Application to the study of mutations causing hereditary elliptocytosis.
1989 StandoutNobel
Population History and Natural Selection Shape Patterns of Genetic Variation in 132 Genes
2004
Defects in a cell cycle checkpoint may be responsible for the genomic instability of cancer cells
1992 StandoutNobel
HIF-Dependent Antitumorigenic Effect of Antioxidants In Vivo
2007 StandoutNobel
A novel polymorphism associated with lactose tolerance in Africa: multiple causes for lactase persistence?
2006
The β-Thalassemias
1999 Standout
Human and Chimpanzee Gene Expression Differences Replicated in Mice Fed Different Diets
2008 StandoutNobel
Factors contributing to anemia after uncomplicated falciparum malaria.
2001
Genetic Signatures of Strong Recent Positive Selection at the Lactase Gene
2004
1 The population genetics of the haemoglobinopathies
1998
6 β-Thalassaemia
1993
The Molecular Genetics of Crop Domestication
2006 Standout
Allele sharing at six VNTR loci and genetic distances among three ethnically defined human populations
1992
Neural-Tube Defects
1999 Standout
LD Score regression distinguishes confounding from polygenicity in genome-wide association studies
2015 Standout
Principal components analysis corrects for stratification in genome-wide association studies
2006 Standout
Disruption of oxygen homeostasis underlies congenital Chuvash polycythemia
2002 StandoutNobel
The Rise and Fall of the Chemoattractant Receptor GPR33
2005 StandoutNobel
Defective neurogenesis resulting from DNA ligase IV deficiency requires Atm
2000 StandoutNobel
Cleft lip and palate
2009 Standout
Hemoglobin SE disease—A concise review
2007
Malaria
2013 Standout
Transcriptional regulation of the lactase-phlorizin hydrolase gene by polymorphisms associated with adult-type hypolactasia
2003
8 The population genetics of the haemoglobinopathies
1993
High resolution of human evolutionary trees with polymorphic microsatellites
1994 StandoutNature
Polyphenols: food sources and bioavailability
2004 Standout
Diet rapidly and reproducibly alters the human gut microbiome
2013 StandoutNature
5 α-Thalassaemia
1993
Sickle-cell disease
2010 Standout
Antioxidant N-acetyl cysteine reduces incidence and multiplicity of lymphoma in Atm deficient mice
2006
Carriage, quantification, and predominance of methanogens and sulfate-reducing bacteria in faecal samples
2006
The weirdest people in the world?
2010 Standout
Dietary flavonoid and isoflavone glycosides are hydrolysed by the lactase site of lactase phlorizin hydrolase
2000
Global, Regional, and National Consumption of Sugar-Sweetened Beverages, Fruit Juices, and Milk: A Systematic Assessment of Beverage Intake in 187 Countries
2015
Heterozygous Germline Mutations in the p53 Homolog p63 Are the Cause of EEC Syndrome
1999
Homology requirements for unequal crossing over in humans.
1991 StandoutNobel
Crystal Structures of the Ribosome in Complex with Release Factors RF1 and RF2 Bound to a Cognate Stop Codon
2005 StandoutNobel
World distribution of factor V Leiden
1995 Standout
Evidence for Gradients of Human Genetic Diversity Within and Among Continents
2004 StandoutNobel
Earliest evidence for cheese making in the sixth millennium bc in northern Europe
2012 Nature
The Origins of Lactase Persistence in Europe
2009
Why are some genetic diseases common?
1993
The Human Condition—A Molecular Approach
2014 StandoutNobel
Genetics and Epidemiology of Adult-type Hypolactasia
1994
Genome-wide detection and characterization of positive selection in human populations
2007 StandoutNature
Evidence for multiple origins of the beta E-globin gene in Southeast Asia.
1982
Involutional Osteoporosis
1986 Standout
Hemoglobin E in Europeans: further evidence for multiple origins of the beta E-globin gene.
1984
Etiologic Heterogeneity of Neural-Tube Defects
1976
Genetic Structure of Human Populations
2002 StandoutScience
Control of iron deficiency anemia in low- and middle-income countries
2013
An Individual with Hb‐Lepore‐Baltimore‐ δβ‐Thalassaemia in a Yugoslavian Family
1976
GLOBIN MESSENGER RNA IN THE THALASSEMIA SYNDROMES*
1974 StandoutNobel
THE GENETIC DEFECT IN ATAXIA-TELANGIECTASIA
1997
Genetic and Fossil Evidence for the Origin of Modern Humans
1988 StandoutScience
Human beta-globin messenger RNA. III. Nucleotide sequences derived from complementary DNA.
1977
Genetic Differences Within and Between Populations of the Major Human Subgroups
1980
Hemoglobin 3α Chains in Apes
1973
A ChineseGγ+(Aγδβ)0thalassemia deletion: comparison to other deletions in the human β-globin gene cluster and sequence analysis of the breakpoints
1985 StandoutNobel
Nucleotide Sequences of Human Globin Messenger RNA
1974 StandoutNobel
Dietary and Policy Priorities for Cardiovascular Disease, Diabetes, and Obesity
2016 Standout
Haemoglobin Constant Spring—A Chain Termination Mutant ?
1971 Nature
Pleistocene North African genomes link Near Eastern and sub-Saharan African human populations
2018 StandoutScienceNobel
3′ Non-coding region sequences in eukaryotic messenger RNA
1976 StandoutNature
Activation of the ATM Kinase by Ionizing Radiation and Phosphorylation of p53
1998 StandoutScience
Identification of the Cystic Fibrosis Gene: Genetic Analysis
1989 StandoutScience
A mutant affecting the heavy chain of myosin in Caenorhabditis elegans
1974 StandoutNobel
Social intelligence, innovation, and enhanced brain size in primates
2002 Standout
Effect of N -Acetyl Cysteine on Oxidative DNA Damage and the Frequency of DNA Deletions in Atm -Deficient Mice
2004
Erythrocyte Enzymopathies in the Newborn
1981
Calcium nutrition and bone health in the elderly
1982
p63 identifies keratinocyte stem cells
2001 Standout
Iron-Deficiency Anemia
2015 Standout
Birds, behavior, and anatomical evolution.
1983
A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences
1980 Standout
Glucose-6-Phosphate Dehydrogenase Deficiency and Hyperbilirubinemia in the Newborn
1971
Selfish DNA: the ultimate parasite
1980 StandoutNature
Red cell metabolism. A. Defects not causing hemolytic disease. B. Environmental modification.
1972
Cloning Human Fetal γ Globin and Mouse α-Type Globin DNA: Characterization and Partial Sequencing
1978 StandoutScienceNobel
Glucose-6-phosphate dehydrogenase deficiency
2008 Standout
The forms of tRNATrp found in avian sarcoma virus and uninfected chicken cells have structural identity but functional distinctions.
1980 StandoutNobel
Characterization of reticulocyte release factor.
1977
Enhanced Phosphorylation of p53 by ATM in Response to DNA Damage
1998 StandoutScience
The Structure and Function of Chromatin
1972
δβ‐Thalassaemia in a Chinese Family
1972
Red cell metabolism
1972
Crop manuring and intensive land management by Europe’s first farmers
2013 Standout
Hydrops Fetalis Caused by α-Thalassemia: An Emerging Health Care Problem
1998
Evolution at Two Levels in Humans and Chimpanzees
1975 StandoutScience
Vesicle formation during reticulocyte maturation. Association of plasma membrane activities with released vesicles (exosomes).
1987 Standout
An argument for the genetic simplicity of man and other mammals
1972
Hemoglobin Wayne: a frameshift mutation detected in human hemoglobin alpha chains.
1976
Works of G. Flatz being referenced
Distribution of Human Adult Lactase Phenotypes in Egypt
1982
GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY AND JAUNDICE IN NEWBORN INFANTS IN NORTHERN THAILAND.
1964
Prevalence of primary adult lactose malabsorption in Hungary
1983
Alpha-Thalassemia in Northern Thailand
1988
Prevalence of α-thalassemias in northern Thailand
1996
Mediterranean types of ?-thalassemia in the German population
1990
DNA Haplotypes and Frameworks Associated with the Beta-Globin Gene in the Kachari Population of Assam (India)
1988
The distribution of the Hb Constant Spring gene in Southeast Asian populations
1990
The spectrum of ?-thalassemia mutations in northern and northeastern Thailand
1989
DNA haplotypes and frameworks linked to the ?-globin locus in an Austro-Asiatic population with a high prevalence of hemoglobin E
1989
?-Globin gene linked DNA haplotypes and frameworks in three South-East Asian populations
1988
Study of Alpha-Thalassemia in Northeastern Thailand at the DNA Level
1990
Chromosome breakage and blastic transformation of lymphocytes in ataxia-telangiectasia
1967
Distribution of human adult lactase phenotypes in the population of Austria
1982
Distribution of adult lactase phenotypes in Bedouins and in urban and agricultural populations of Jordan.
1983
Distribution of physiological adult lactase phenotypes, lactose absorber and malabsorber, in Germany
1982
Prevalence of primary adult lactose malabsorption in three populations of northern China
1984
Fronto-ethmoidal encephalomeningoceles in the population of northern Thailand
1970
Gene-dosage effect on intestinal lactase activity demonstrated in vivo.
1984
Beja And Nilotes: Nomadic pastoralist groups in the Sudan with opposite distributions of the adult lactase phenotypes
1982
Hemoglobinopathies in Northeast India
1987
Prevalence of primary adult lactose malabsorption and awareness of milk intolerance in Italy
1984
Polymorphism of erythrocyte phosphoglucomutase, adenylate kinase and adenosine deaminase in northern Thailand
1972
NEONATAL JAUNDICE IN GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY
1963
LACTOSE NUTRITION AND NATURAL SELECTION
1973
Glucose-6-Phosphate Dehydrogenase Deficiency and Neonatal Jaundice
1963
Distribution of the adult lactase phenotypes in Turkey.
1986
The human lactase polymorphism: physiology and genetics of lactose absorption and malabsorption.
1977
Prevalence of primary adult lactose malabsorption in Poland
1984
X-Chromosomally inherited split-hand/split-foot anomaly in a Pakistani kindred
1987
Pulmonary Hydrogen and Methane Excretion Following Ingestion of an Unabsorbable Carbohydrate
1985
Haemoglobinopathies in Thailand. II. INCIDENCE AND DISTRIBUTION OF ELEVATIONS OF HAEMOGLOBIN A2 AND HAEMOGLOBIN F; A SURVEY OF 2790 PEOPLE
1965
Hemoglobin Suan-Dok (α2109(G16)LEU-ARGβ2). an Unstable Variant Associated with α-Thalassemia
1979
Hemoglobin E: Distribution and population dynamics
1967
Lactose Intolerance in Thailand
1969 Nature
Distribution of the lactase phenotypes in the population of the Democratic Republic of the Sudan
1981
Population study of erythrocyte glutathione reductase activity
1971
A study of lactose absorption capacity in twins
1984
Evidence against nutritional adaption of tolerance to lactose
1971
HÆMOGLOBIN TAK: A VARIANT WITH ADDITIONAL RESIDUES AT THE END OF THE β-CHAINS
1971
Distribution of the adult lactase phenotypes--lactose absorber and malabsorber--in a group of 131 army recruits.
1982
Lactose Tolerance in Asians: a Family Study
1969 Nature
Genetics of Lactose Digestion in Humans
1987
Distribution of adult lactase phenotypes in the Tuareg of Niger.
1986
Haemoglobin Tak: a β‐Chain Elongation
1975
Persistence of high intestinal lactase activity (lactose tolerance) in Afghanistan
1976