The Finnish population structure A genetic and genealogical study

Zone electrophoresis in starch gels: group variations in the serum proteins of normal human adults

1955 • 2,812 citations

Blood groups in man

1962 • 1,174 citations

On a Matching Problem Arising in Genetics

1949 • 1,048 citations

THE ESTIMATION AND SIGNIFICANCE OF THE LOGARITHM OF A RATIO OF FREQUENCIES

1956 • 1,026 citations

THE MEASUREMENT OF TASTE SENSITIVITY TO PHENYLTHIOUREA (P.T.C.)

1949 • 463 citations

The Distribution of the Human Blood Groups

1955 • 456 citations

IMMUNE‐ELECTROPHORETIC DEMONSTRATION OF QUALITATIVE DIFFERENCES IN HUMAN SERA AND THEIR RELATION TO THE HAPTOGLOBINS

1959 • 306 citations

ASPARTYLGLYCOSAMINURIA

1968 • 266 citations

Selective Vitamin B₁₂ Malabsorption and Proteinuria in Young People A Syndrome

1960 • 227 citations

Population Genetics and Evolution

2012 • 223 citations

Familial systemic paramyloidosis with lattice dystrophy of the cornea, progressive cranial neuropathy, skin changes and various internal symptoms. A previously unrecognized heritable syndrome.

1969 • 215 citations

Comparison of genetical and morphological methods for a study of biological differences

1953 • 183 citations

Idiopathic Chronic Megaloblastic Anemia in Children

1960 • 174 citations

The Red Cell Phenotype En(a‐) and Anti‐En^a: Serological and Physicochemical Aspects

1969 • 109 citations

Nephrotic syndrome in newborn and young infants.

1956 • 107 citations

POPULATION GENETICS AND EVOLUTION

1970 • 104 citations

Human Genetics: Principles and Methods

1962 • 94 citations

Dystrophia retinae pigmentosa--dysacusis syndrome (DRD): a study of the Usher- or Hallgren syndrome.

1970 • 84 citations

Familial Protein Intolerance with Deficient Transport of Basic Amino Acids: An Analysis of 10 Patients

1967 • 77 citations

THE Rh CHROMOSOME FREQUENCIES IN ENGLAND

1948 • 74 citations

A general program for maximum likelihood estimation of gene frequencies.

1967 • 73 citations

Human genetics : principles and methods

1961 • 71 citations

TRANSFERRIN VARIATION IN COLUMBIDAE

1962 • 70 citations

A new antigen and antibody belonging to the P blood group system.

1959 • 65 citations

INDIVIDUAL PRECIPITATION PATTERNS OF NORMAL RABBIT SERA

1959 • 63 citations

A ‘New’ Kell Blood-Group Phenotype

1957 • 60 citations

HISTOPATHOLOGICAL FINDINGS OF FAMILIAL AMYLOIDOSIS WITH CRANIAL NEUROPATHY AS PRINCIPAL MANIFESTATION

1971 • 48 citations

Disaccharidases and Histology of Duodenal Mucosa in Congenital Lactose Malabsorption

1966 • 42 citations

The Red Cell Antigen P^k and its Relationship to the P System: the Evidence of Three More P^k Families

1965 • 36 citations

MYOCLONUS EPILEPSY (UNVERRICHT-LUNDBORG) IN FINLAND

2009 • 34 citations

FAMILIAL PROTEIN INTOLERANCE WITH DEFICIENT TRANSPORT OF BASIC AMINO ACIDS

1968 • 34 citations

ELEVEN NEW CASES OF ASPARTYLGLUCOSAMINURIA*

1970 • 33 citations

A SIMPLE METHOD OF DETERMINING HAPTOGLOBIN GROUPS IN HUMAN SERA BY MEANS OF AGAR‐GEL ELECTROPHORESIS

1959 • 32 citations

Non-parasitic cysts of the liver. A clinical study of 117 cases.

1970 • 30 citations

PREVALENCE OF PHENYLKETONURIA AND SOME OTHER METABOLIC DISORDERS AMONG MENTALLY RETARDED PATIENTS IN FINLAND

1967 • 28 citations

The Nephrotic Syndrome and Heredity

1969 • 28 citations

No Evidence of Active Renin-Inhibitors in Plasma. The Kinetics of the Reaction between Renin and Substrate in Non-pre-treated Plasma

1971 • 23 citations

Familial chloride diarrhea-chloride malabsorption.

1968 • 22 citations

The Distribution of the Transferrin Variants D<sub>1</sub> and D<sub>chi</sub> in Various Populations

1964 • 21 citations

Congenital Deficiency of Fibrin Stabilizing Factor

1962 • 21 citations

A study in the morphology of the Finns and its relation to the settlement of Finland.

1971 • 17 citations

Selective Malabsorption of Vitamin B12

1963 • 17 citations

Distribution of serum transferrin groups in Finland and their inheritance.

1965 • 17 citations

STUDIEN ÜBER CORNEA PLANA CONGENITA BEI 19 KRANKEN IN 9 FAMILIEN

1961 • 16 citations

Rare Congenital Coagulation Factor Defects in Finland

1971 • 16 citations

The Blood Group Antigen Ul^a (Karhula)

1968 • 15 citations

TRANSFERRIN VARIANTS IN LAPPS AND SWEDES

1961 • 15 citations

An Inherited Blood Group A Variant in the Finnish Population

1973 • 15 citations

Population genetic studies of the indigenous peoples of Australia and New Guinea.

1965 • 14 citations

GENETICAL STUDIES ON THE Rh BLOOD GROUP SYSTEM

2009 • 11 citations

TASTE‐DEFICIENCY IN LAPPISH AND FINNISH POPULATIONS

1953 • 11 citations

Clinical findings in three patients with nonketotic hyperglycinaemia.

1970 • 7 citations

Progressive Myoclonus Epilepsy

2008 • 7 citations

The Pedigrees of Two People Already Reported as of Phenotype K‐, k‐, Kp(a‐b‐)

1961 • 7 citations

[Cornea plana congenita].

1972 • 5 citations

[X-chromosomal recessive retinoschisis].

1972 • 4 citations

[Inborn errors of amino acid metabolism].

1972 • 3 citations

Progressive Myoclonus with Epilepsy

1972 • 2 citations

Selective Malabsorption of Vitamin B₁₂

1968 • 2 citations

[The distribution of blood and serum groups in a Finnish population living around Leningrad (Ingria) through ten generations].

1970 • 1 citations

[Chloride diarrhea and lactose malabsorption].

1972 • 1 citations

[Aspartylglucosaminuria].

1972 • 1 citations