Standout Papers
Citation Impact
Citing Papers
Requirement of bic/microRNA-155 for Normal Immune Function
2007 StandoutScience
Gene Dose of Apolipoprotein E Type 4 Allele and the Risk of Alzheimer's Disease in Late Onset Families
1993 StandoutScience
A Neuroligin-3 Mutation Implicated in Autism Increases Inhibitory Synaptic Transmission in Mice
2007 StandoutScienceNobel
Serum Albumin
1985 Standout
Schizophrenia risk from complex variation of complement component 4
2016 StandoutNature
Familial alzheimer's disease in american descendants of the volga germans: Probable genetic founder effect
1988
The foreign antigen binding site and T cell recognition regions of class I histocompatibility antigens
1987 StandoutNature
Shared genetic susceptibility of Type 1 (insulin-dependent) and Type 2 (non-insulin-dependent) diabetes mellitus: contributions of HLA and haptoglobin
1991
A family of candidate taste receptors in human and mouse
2000 StandoutNatureNobel
Genetic analysis of IDDM: Summary of GAW5 IDDM results
1989
Idiopathic dystonia among ashkenazi jews: Evidence for autosomal dominant inheritance
1989
Common West African HLA antigens are associated with protection from severe malaria
1991 StandoutNature
Structure of the human class I histocompatibility antigen, HLA-A2
1987 StandoutNature
Mapping of a gene predisposing to early–onset Alzheimer's disease to chromosome 14q24.3
1992
Pheromonal communication in vertebrates
2006 Nature
A locus for familial early–onset Alzhelmer's disease on the long arm of chromosome 14, proximal to the α1–antichymotrypsin gene
1992
Maternal-fetal interactions and the maintenance of HLA polymorphism.
1988
Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32–34
1990
Limb malformations and the human HOX genes
2002
PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses
2007 Standout
Structure of Serum Albumin
1994 Standout
Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder population
1995
The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein
1997 Standout
Searching for ways out of the autism maze: genetic, epigenetic and environmental clues
2006
Genome-wide search for asthma susceptibility loci in a founder population. The Collaborative Study on the Genetics of Asthma
1998
Atomic structure and chemistry of human serum albumin
1992 StandoutNature
HLA-DQβ gene contributes to susceptibility and resistance to insulin-dependent diabetes mellitus
1987 StandoutNature
Molecular Genetics of Alzheimer's Disease
1993
Implantation and the placenta: key pieces of the development puzzle
1994 StandoutScience
Mapping and conservation of the group-specific component gene in mouse
1990
Mutations in genetic variants of human serum albumin found in Italy.
1990
Linkage and mutational analysis of familial Alzheimer disease kindreds for the APP gene region.
1992
The human T-cell receptor α-chain gene maps to chromosome 14
1985 StandoutNatureNobel
Polymorphic DNA haplotypes at the human phenylalanine hydroxylase locus and their relationship with phenylketonuria
1987
Expression of recessive alleles by chromosomal mechanisms in retinoblastoma
1983 StandoutNature
A gene required for class II-restricted antigen presentation maps to the major histocompatibility complex.
1991
Identical structural changes in inherited albumin variants from different populations.
1989
The Major Histocompatibility Complex — Genetics and Biology
1976
A molecular map of the human major histocompatibility complex class III region linking complement genes C4, C2 and factor B
1984 Nature
Interactive effect of Gm allotypes and HLA-B locus antigens on the human antibody response to a bacterial antigen.
1980
An Increased Percentage of Long Amyloid β Protein Secreted by Familial Amyloid β Protein Precursor (βApp 717 ) Mutants
1994 StandoutScience
Population amalgamation and genetic variation: observations on artificially agglomerated tribal populations of Central and South America.
1988
Recognition of Stress-Induced MHC Molecules by Intestinal Epithelial γδ T Cells
1998 StandoutScience
Genetic Structure of Human Populations
2002 StandoutScience
Relation of insulin‐dependent diabetes mellitus (IDD) and the HLA‐linked SB system
1984
Determination of the Tryptophan Content of Proteins by Ion Exchange Chromatography of Alkaline Hydrolysates
1972 StandoutNobel
The locus for apolipoprotein E (apoE) is linked to the complement component C3 (C3) locus on chromosome 19 in man
1982
Eight Types of Bisalbuminaemia
1970 Nature
A Century of Alzheimer's Disease
2006 StandoutScience
Serum Albumin
1970
Reconstructing the DNA Methylation Maps of the Neandertal and the Denisovan
2014 StandoutScienceNobel
Olfactory neurons expressing transient receptor potential channel M5 (TRPM5) are involved in sensing semiochemicals
2007 StandoutNobel
An intronless gene encoding a potential member of the family of receptors coupled to guanine nucleotide regulatory proteins
1987 StandoutNatureNobel
Human DNA ligase I cDNA: cloning and functional expression in Saccharomyces cerevisiae.
1990 StandoutNobel
Genetic Differences Within and Between Populations of the Major Human Subgroups
1980
The pronatriodilatin gene is located on the distal short arm of human chromosome 1 and on mouse chromosome 4.
1985
Autism-linked neuroligin-3 R451C mutation differentially alters hippocampal and cortical synaptic function
2011 StandoutNobel
Serum vitamin D-binding protein is a third member of the albumin and alpha fetoprotein gene family.
1985
Assignment of first random restriction fragment length polymorphism (RFLP) locus ((D14S1) to a region of human chromosome 14.
1982
A genetically clamped renin transgene for the induction of hypertension
2002 StandoutNobel
Identification of the Cystic Fibrosis Gene: Genetic Analysis
1989 StandoutScience
Paralogous mouse Hox genes, Hoxa9, Hoxb9, and Hoxd9, function together to control development of the mammary gland in response to pregnancy
1999 StandoutNobel
Candidate Gene for the Chromosome 1 Familial Alzheimer's Disease Locus
1995 StandoutScience
Global Patterns of Linkage Disequilibrium at the CD4 Locus and Modern Human Origins
1996 StandoutScienceNobel
Genetic and linguistic differentiation in the Americas.
1993 StandoutNobel
Apolipoprotein E: Cholesterol Transport Protein with Expanding Role in Cell Biology
1988 StandoutScience
Invasive equine trophoblast expresses conventional class I Major Histocompatibility Complex antigens
1990
A comparison of sib‐pair linkage tests for disease susceptibility loci
1985
The Future of Genetic Studies of Complex Human Diseases
1996 StandoutScience
Amino acid substitutions in inherited albumin variants from Amerindian and Japanese populations.
1987
Multiple DNA fragment polymorphisms associated with immunoglobulin mu chain switch-like regions in man.
1983 StandoutNobel
Genetic Dissection of Complex Traits
1994 StandoutScience
Genetics of Type I diabetes mellitus: a single, recessive predisposition gene mapping between HLA-B and GLO. With an appendix on the estimation of selection bias.
1981
cDNA for the human beta 2-adrenergic receptor: a protein with multiple membrane-spanning domains and encoded by a gene whose chromosomal location is shared with that of the receptor for platelet-derived growth factor.
1987 StandoutNobel
Preface to the proceedings of the workshop on genetic management of captive populations
1986
Bipolar affective disorders linked to DNA markers on chromosome 11
1987 Nature
Assignment of the major histocompatibility complex to a region of the short arm of human chromosome 6.
1977
Isolation and properties of serum albumin from the house mouse Mus musculus
1976
Tyrosine Kinase Receptor with Extensive Homology to EGF Receptor Shares Chromosomal Location with neu Oncogene
1985 StandoutScience
Localization of the human α-globin structural gene to chromosome 16 in somatic cell hybrids by molecular hybridization assay
1977
The distribution of red cell enzyme and serum protein groups in a population of Dani (Pit River, West Irian)
1973
Dynamic Kinetic Resolution of Racemic β-Haloalcohols: Direct Access to Enantioenriched Epoxides
2008 StandoutNobel
Clones from the human gene complex coding for salivary proline-rich proteins.
1984 StandoutNobel
Cloning, Sequencing, and Expression of the Gene Coding for the Human Platelet α 2 -Adrenergic Receptor
1987 StandoutScienceNobel
Genetic polymorphism of CON 1 and CON 2 salivary proteins detected by immunologic and concanavalin a reactions on nitrocellulose with linkage of CON 1 and CON 2 genes to the SPC (salivary protein gene complex)
1984
Candidate autism gene screen identifies critical role for cell-adhesion molecule CASPR2 in dendritic arborization and spine development
2012 StandoutNobel
Assignment of the structural gene for the third component of human complement to chromosome 19.
1982
Senile dementia of the Alzheimer type
1983
Alzheimer's Disease: Cell-Specific Pathology Isolates the Hippocampal Formation
1984 StandoutScience
Genetics and Demography in Biological Conservation
1988 StandoutScience
Linkage analysis of familial Alzheimer disease, using chromosome 21 markers.
1991
Genetic Variation Among Vertebrate Species
1973
Association of Anxiety-Related Traits with a Polymorphism in the Serotonin Transporter Gene Regulatory Region
1996 StandoutScience
Evolution at Two Levels in Humans and Chimpanzees
1975 StandoutScience
Genetic Linkage Evidence for a Familial Alzheimer's Disease Locus on Chromosome 14
1992 Science
Guam Amyotrophic Lateral Sclerosis-Parkinsonism-Dementia Linked to a Plant Excitant Neurotoxin
1987 StandoutScience
Gene dosage-dependent effects of the Hoxa-13 and Hoxd-13 mutations on morphogenesis of the terminal parts of the digestive and urogenital tracts
1997
Differences in human α- and β-globin gene expression in mouse erythroleukemia cells: The role of intragenic sequences
1984 StandoutNobel
Works of L.R. Weitkamp being referenced
An Electrophoretic Comparison of Human Serum Albumin Variants: Eight Distinguishable Types
1969
Unusual Albumin Variants in Indonesians and Malayan Aborigines
1971
The Linkage Relationships of HL-A with other Genetic Marker Systems
1975
The Relation of Parental Sex and Age to Recombination in the HL-A System
1973 StandoutNobel
An Electrophoretic Comparison of Serum Albumin Variants from Nineteen Unrelated Families
1967
Linkage Between the MN- and Hb β-Loci?
1972
Additional Data and Summary for Albumin-Gc Linkage in Man
1970
HLA and Mate Choice in Humans
1997
Discovery of allelic variants ofHOXA1 andHOXB1: Genetic susceptibility to autism spectrum disorders
2000
Human serum albumin: twenty‐three genetic variants and their population distribution
1973
Serum Albumin Variants in New Guinea Indigenes
1969
The genetic structure of a tribal population, the Yanomama Indians: III. Seven serum protein systems*
1972
Familial Alzheimer's disease in two kindreds of the same geographic and ethnic origin
1981 Nobel
Allelic specific heterogeneity in the <i>Pi:Gm</i> linkage group
1978
Genetic linkage between structural loci for albumin and group specific component (Gc).
1966
Report of the committee on the genetic constitution of chromosome 6
1982
Alzheimer disease: evidence for susceptibility loci on chromosomes 6 and 14.
1983
Genetic variability, inbreeding, and reproductive performance in standardbred horses
1986
The genetic structure of a tribal population, the Yanomama Indians: IV. Eleven erythrocyte enzymes and summary of protein variants*
1972
EVOLUTIONARY CONSERVATION OF EQUINE Gc ALLELES AND OF MAMMALIAN Gc/ALBUMIN LINKAGE
1979
On the Mapping of PGM3, GLO and HLA
1978
Human leukocyte antigen matching and fetal loss: results of a 10 year prospective study
1998
Genetic linkage relations of the loci for 6-phosphogluconate dehydrogenase and adenosine deaminase in man.
1970
Probable Genetic Linkage between the Loci for the Lewis Blood Group and Complement C 3
1974
Amino acid substitution in two identical inherited human serum albumin variants. Albumin Oliphant and albumin Ann Arbor
1972
The hand-foot-uterus syndrome
1970
Genetic heterogeneity of insulin-dependent (type I) diabetes mellitus: evidence from a study of extended haplotypes.
1984
Genetic linkage between a locus for 6-PGD and the Rh locus: evaluation of possible heterogeneity in the recombination fraction between sexes and among families.
1971
Additional data on the population distribution of human serum albumin genes; three new variants
1973
Depressive Disorders and HLA: A Gene on Chromosome 6 That Can Affect Behavior
1981
ELA and fertility in American Standardbred horses
1988
Parental HLA compatibility, fetal wastage and neural tube defects: evidence for a T/t-like locus in humans.
1984
Albumin Máku: a New Variant of Human Serum Albumin
1968 Nature
The influence of cultural factors on the demography and pattern of gene flow from the Makiritare to the Yanomama Indians
1970
Gm, Km, and HLA in Insulin-Dependent Type I Diabetes Mellitus: A Log-Linear Analysis of Association
1986