| human | Q5 |
| P496 | ORCID iD | 0000-0002-2001-3904 |
| P735 | given name | Peter | Q2793400 |
| Peter | Q2793400 | ||
| P106 | occupation | researcher | Q1650915 |
| P21 | sex or gender | male | Q6581097 |
| Q34140192 | A common variant of PNPLA3 (p.I148M) is not associated with alcoholic chronic pancreatitis |
| Q84920409 | A genetic variant in the pre-miR-27a oncogene is associated with a reduced familial breast cancer risk |
| Q37660241 | A recombined allele of the lipase gene CEL and its pseudogene CELP confers susceptibility to chronic pancreatitis |
| Q53315710 | A variant affecting a putative miRNA target site in estrogen receptor (ESR) 1 is associated with breast cancer risk in premenopausal women. |
| Q40790139 | Apolipoprotein E allele frequencies in chronic and self-limited hepatitis C suggest a protective effect of APOE4 in the course of hepatitis C virus infection |
| Q94355861 | Association of () polymorphisms with breast cancer risk |
| Q46402532 | Association of NCOA3 polymorphisms with breast cancer risk |
| Q46707380 | Association of a common AKAP9 variant with breast cancer risk: a collaborative analysis |
| Q54657396 | Association of death receptor 4 haplotype 626C-683C with an increased breast cancer risk. |
| Q53651814 | Association of the CASP10 V410I variant with reduced familial breast cancer risk and interaction with the CASP8 D302H variant. |
| Q33284720 | BRIP1 (BACH1) variants and familial breast cancer risk: a case-control study |
| Q34379032 | Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium |
| Q34002454 | Copy number variant in the candidate tumor suppressor gene MTUS1 and familial breast cancer risk |
| Q35009015 | Evaluation of SNPs in miR-146a, miR196a2 and miR-499 as low-penetrance alleles in German and Italian familial breast cancer cases |
| Q51580354 | Expression of collagen and fiber-associated proteins in human septal cartilage during in vitro dedifferentiation. |
| Q37636741 | Functional single nucleotide polymorphisms within the cyclin-dependent kinase inhibitor 2A/2B region affect pancreatic cancer risk |
| Q34292747 | Genetic analyses of heme oxygenase 1 (HMOX1) in different forms of pancreatitis |
| Q43538243 | Genetic susceptibility to pancreatic cancer and its functional characterisation: the PANcreatic Disease ReseArch (PANDoRA) consortium |
| Q53291654 | Genetic variants within miR-126 and miR-335 are not associated with breast cancer risk. |
| Q34378972 | Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade |
| Q44752870 | Genetic variation in the major mitotic checkpoint genes does not affect familial breast cancer risk |
| Q45087021 | Genome-wide analysis associates familial colorectal cancer with increases in copy number variations and a rare structural variation at 12p12.3. |
| Q40103441 | Genome-wide association study identifies inversion in the CTRB1-CTRB2 locus to modify risk for alcoholic and non-alcoholic chronic pancreatitis |
| Q43617306 | Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease |
| Q44028747 | Identification of a DMBT1 polymorphism associated with increased breast cancer risk and decreased promoter activity |
| Q50483549 | In vitro analysis of matrix proteins and growth factors in dedifferentiating human chondrocytes for tissue-engineered cartilage |
| Q35104068 | Inherited variants in the inner centromere protein (INCENP) gene of the chromosomal passenger complex contribute to the susceptibility of ER-negative breast cancer |
| Q96691996 | KDAS, a new blood group antigen in the Knops blood group system antithetical to KCAM |
| Q57610440 | Lack of Replication of Seven Pancreatic Cancer Susceptibility Loci Identified in Two Asian Populations |
| Q36179367 | Length of Variable Numbers of Tandem Repeats in the Carboxyl Ester Lipase (CEL) Gene May Confer Susceptibility to Alcoholic Liver Cirrhosis but Not Alcoholic Chronic Pancreatitis |
| Q37225243 | New susceptibility locus for coronary artery disease on chromosome 3q22.3. |
| Q33583309 | Nuclear receptor coregulator SNP discovery and impact on breast cancer risk |
| Q43613530 | Polymorphisms in genes involved in GH1 release and their association with breast cancer risk |
| Q46585200 | Re: Association of a common variant of the CASP8 gene with reduced risk of breast cancer |
| Q80442969 | SNPs in ultraconserved elements and familial breast cancer risk |
| Q24810703 | TP53-binding protein variants and breast cancer risk: a case-control study |
| Q33300099 | The CASP8 -652 6N del promoter polymorphism and breast cancer risk: a multicenter study |
| Q45154642 | The rare ERBB2 variant Ile654Val is associated with an increased familial breast cancer risk |
| Q53639998 | The single nucleotide polymorphism IVS1+309 in mouse double minute 2 does not affect risk of familial breast cancer. |
| Q98879766 | Two novel antithetical KN blood group antigens may contribute to more than a quarter of all KN antisera in Europe |
| Q37540036 | Variants in CPA1 are strongly associated with early onset chronic pancreatitis |
| Q46521646 | c-MYC Asn11Ser is associated with increased risk for familial breast cancer |
Search more.