Citation Impact
Citing Papers
Computational protein design enables a novel one-carbon assimilation pathway
2015 StandoutNobel
Epigenetic memory of active gene transcription is inherited through somatic cell nuclear transfer
2005 StandoutNobel
Epigenetic Transgenerational Actions of Endocrine Disruptors and Male Fertility
2005 StandoutScience
X-linked cholestasis in mouse due to mutations of the P4-ATPase ATP11C
2011 StandoutNobel
Frequent deletions and down-regulation of micro- RNA genes miR15 and miR16 at 13q14 in chronic lymphocytic leukemia
2002 Standout
Podocin and MEC-2 bind cholesterol to regulate the activity of associated ion channels
2006 StandoutNobel
Engineering BioBrick vectors from BioBrick parts
2008
Comprehensive molecular portraits of human breast tumours
2012 StandoutNature
Analysis of the genome sequence of the flowering plant Arabidopsis thaliana
2000 StandoutNature
The human olfactory receptor gene family
2004 StandoutNobel
Cntnap2 is disrupted in a family with gilles de la tourette syndrome and obsessive compulsive disorder
2003
BAC representation of two low‐copy regions of the genome of Arabidopsis thaliana
1998
A Bacterial Artificial Chromosome Library for Sequencing the Complete Human Genome
2001
Construction and preliminary analysis of the ICRF human P1 library
1994
Epigenetics in human disease and prospects for epigenetic therapy
2004 StandoutNature
Construction of a 780-kb PAC, BAC, and Cosmid Contig Encompassing the Minimal Critical Deletion Involved in B Cell Chronic Lymphocytic Leukemia at 13q14.3
1997
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
1998 StandoutNature
Prader-Willi syndrome: advances in genetics, pathophysiology and treatment
2003
A Mutant Drosophila Homolog of Mammalian Clock Disrupts Circadian Rhythms and Transcription of period and timeless
1998 StandoutNobel
The ground state of embryonic stem cell self-renewal
2008 StandoutNature
A Spatial Map of Olfactory Receptor Expression in the Drosophila Antenna
1999 StandoutNobel
22q11.21 Deletion Syndromes: A Review of Proximal, Central, and Distal Deletions and Their Associated Features
2015 Standout
Mutations Involving the Transcription Factor CBFA1 Cause Cleidocranial Dysplasia
1997 Standout
Comprehensive analysis of a large genomic sequence at the putative B-cell chronic lymphocytic leukaemia (B-CLL) tumour suppresser gene locus
2001
Genome sequence of the endocellular bacterial symbiont of aphids Buchnera sp. APS
2000 StandoutNature
Osf2/Cbfa1: A Transcriptional Activator of Osteoblast Differentiation
1997 Standout
Immunogenicity of induced pluripotent stem cells
2011 StandoutNature
Epigenetic reprogramming in mouse primordial germ cells
2002
ASC, a Novel 22-kDa Protein, Aggregates during Apoptosis of Human Promyelocytic Leukemia HL-60 Cells
1999
β-Lactam antibiotics offer neuroprotection by increasing glutamate transporter expression
2005 StandoutNature
A new logic for DNA engineering using recombination in Escherichia coli
1998
DMY is a Y-specific DM-domain gene required for male development in the medaka fish
2002 StandoutNature
Parent-Specific Complementary Patterns of Histone H3 Lysine 9 and H3 Lysine 4 Methylation at the Prader-Willi Syndrome Imprinting Center
2001
Homologous recombination based modification in Esherichia coli and germline transmission in transgenic mice of a bacterial artificial chromsome
1997
An Improved Approach for Construction of Bacterial Artificial Chromosome Libraries
1998
NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome
2000
Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family
1997 Standout
Initial sequence of the chimpanzee genome and comparison with the human genome
2005 StandoutNature
Large-Insert BAC/YAC Libraries for Selective Re-isolation of Genomic Regions by Homologous Recombination in Yeast
2001
Sequence, Structure, and Evolution of a Complete Human Olfactory Receptor Gene Cluster
2000
Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosis
1995 Nature
Gene Silencing in Cancer in Association with Promoter Hypermethylation
2003 Standout
A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasis
1998
A novel method for making nested deletions and its application for sequencing of a 300 kb region of human APP locus
1997
Generation of germline-competent induced pluripotent stem cells
2007 StandoutNatureNobel
A gene expression atlas of the central nervous system based on bacterial artificial chromosomes
2003 StandoutNature
Differential activation of the inflammasome by caspase-1 adaptors ASC and Ipaf
2004 StandoutNature
An integrated metric physical map of human chromosome 19
1995
p63 is a p53 homologue required for limb and epidermal morphogenesis
1999 StandoutNature
GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5
2003 StandoutNature
Chromosome 20 deletions in myeloid malignancies: reduction of the common deleted region, generation of a PAC/BAC contig and identification of candidate genes
2000
Truncating mutations of hSNF5/INI1 in aggressive paediatric cancer
1998 StandoutNature
Bac to the future: The use of bac transgenic mice for neuroscience research
2001
The Retinoblastoma Binding Protein RBP2 Is an H3K4 Demethylase
2007 StandoutNobel
Human BAC library: construction and rapid screening
1997
Highly Efficient Modification of Bacterial Artificial Chromosomes (BACs) Using Novel Shuttle Vectors Containing the R6Kγ Origin of Replication
2002
Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na–K–2CI cotransporter NKCC2
1996
Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia
1996 StandoutNature
Organization and Evolution of Olfactory Receptor Genes on Human Chromosome 11
1998
Role of c-Src Tyrosine Kinase in G Protein-coupled Receptorand Gβγ Subunit-mediated Activation of Mitogen-activated Protein Kinases
1996 StandoutNobel
Gβγ Subunits Mediate Src-dependent Phosphorylation of the Epidermal Growth Factor Receptor
1997 StandoutNobel
A Gain-of-Function Mutation of JAK2 in Myeloproliferative Disorders
2005 Standout
A Genomic Region Encompassing a Cluster of Olfactory Receptor Genes and a Myosin Light Chain Kinase (MYLK) Gene Is Duplicated on Human Chromosome Regions 3q13–q21 and 3p13
1999
The human AQP4 gene: definition of the locus encoding two water channel polypeptides in brain.
1996 StandoutNobel
Paternal and maternal DNA lineages reveal a bottleneck in the founding of the Finnish population.
1996 StandoutNobel
Human specific loss of olfactory receptor genes
2003 StandoutNobel
Primate Evolution of an Olfactory Receptor Cluster: Diversification by Gene Conversion and Recent Emergence of Pseudogenes
1999
Epigenetic Reprogramming in Mammalian Development
2001 StandoutScience
Bacterial artificial chromosome libraries for mouse sequencing and functional analysis.
2000
PKD2 , a Gene for Polycystic Kidney Disease That Encodes an Integral Membrane Protein
1996 StandoutScience
One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products
2000 Standout
Src Family Protein Tyrosine Kinases Induce Autoactivation of Bruton's Tyrosine Kinase
1995
Long oligonucleotide microarrays for African green monkey gene expression profile analysis
2007 StandoutNobel
The genome of Caenorhabditis elegans.
1995 StandoutNobel
The Role of DNA Methylation in Mammalian Epigenetics
2001 StandoutScience
Recombineering: a powerful new tool for mouse functional genomics
2001
Genomic analysis of orthologous mouse and human olfactory receptor loci
2001 StandoutNobel
Candidate autism gene screen identifies critical role for cell-adhesion molecule CASPR2 in dendritic arborization and spine development
2012 StandoutNobel
Constitutive expression of a complement-like protein in Toll and JAK gain-of-function mutants ofDrosophila
2000 StandoutNobel
A P1-based physical map of the Drosophila euchromatic genome.
1996
The Ubiquitin-Proteasome Proteolytic Pathway: Destruction for the Sake of Construction
2002 StandoutNobel
Uncompensated polyuria in a mouse model of Bartter's syndrome
2000 StandoutNobel
The Complete Nucleotide Sequence of the Human Immunoglobulin Heavy Chain Variable Region Locus
1998 StandoutNobel
Conservation of sequence and structure flanking the mouse and human β-globin loci: The β-globin genes are embedded within an array of odorant receptor genes
1999 StandoutNobel
Works of Peter M. Kroisel being referenced
Maternal methylation imprints on human chromosome 15 are established during or after fertilization
2001
TXK, a novel human tyrosine kinase expressed in T cells shares sequence identity with Tec family kinases and maps to 4p12
1994
The human γ-aminobutyric acid A receptor delta (GABRD) gene: molecular characterisation and tissue-specific expression
2002
Candidate region for Gilles de la Tourette syndrome at 7q31
2001
A new bacteriophage P1–derived vector for the propagation of large human DNA fragments
1994