Evidence map›Paper›PMID 24359990›Full record

ReviewAdvances in chronic kidney disease2014

Hereditary kidney cancer syndromes.

Naomi B Haas, Katherine L Nathanson

Abstract readReview
In one paragraph

Review in Advances in chronic kidney disease, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed, 4 pooled it
3.9field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

67 citing papers in PubMed, 4 syntheses or guidelines pooled it, 199 citations in OpenAlex.

  1. Pooled it
  2. Pathway Analysis of Renal Cell Carcinoma Genome-Wide Association Studies Identifies Novel Associations.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2020
    Pooled it
  3. Racial Disparities and Preventive Measures to Renal Cell Carcinoma.International journal of environmental research and public health · 2018
    Pooled it
  4. Pooled it
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  17. Hereditary renal mass syndromes: a pictorial review.Abdominal radiology (New York) · 2025
    Review
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7 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Naomi B HaasDepartment of Medicine, Division of Hematology/Oncology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA; and Department of Medicine, Division of Translational Medicine and Human Genetics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA.
Katherine L NathansonDepartment of Medicine, Division of Hematology/Oncology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA; and Department of Medicine, Division of Translational Medicine and Human Genetics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA. Electronic address: knathans@exchange.upenn.edu.
University of Pennsylvania · US

Funding

Genotype and phenotype predictors in therapy response in renal cell carcinomaR01CA135509 · NCI · UNIVERSITY OF PENNSYLVANIA · PI FLAHERTY, KEITH T, LEE, WILLIAM M · 2009 to 2013
$2.3M
NCI NIH HHS R01 CA135509
6 · The paper itself

Abstract

Inherited susceptibility to kidney cancer is a fascinating and complex topic. Our knowledge about types of genetic syndromes associated with an increased risk of disease is continually expanding. Currently, there are 10 syndromes associated with an increased risk of all types of kidney cancer, which are reviewed herein. Clear cell kidney cancer is associated with von Hippel Lindau disease, chromosome 3 translocations, PTEN hamartomatous syndrome, and mutations in the BAP1 gene as well as several of the genes encoding the proteins comprising the succinate dehydrogenase complex (SDHB/C/D). Type 1 papillary kidney cancers arise in conjunction with germline mutations in MET and type 2 as part of hereditary leiomyomatosis and kidney cell cancer (fumarate hydratase [FH] mutations). Chromophone and oncocytic kidney cancers are predominantly associated with Birt-Hogg-Dubé syndrome. Patients with Tuberous Sclerosis Complex (TSC) commonly have angiomyolipomas and rarely their malignant counterpart epithelioid angiomyolipomas. The targeted therapeutic options for the kidney cancer associated with these diseases are just starting to expand and are an area of active clinical research.

Indexed as

Birt-Hogg-Dube SyndromeCarcinoma, Renal CellChromosomes, Human, Pair 3Genetic Predisposition to DiseaseHamartoma Syndrome, MultipleHumansKidney NeoplasmsLeiomyomatosisNeoplastic Syndromes, HereditaryProto-Oncogene Proteins c-metSkin NeoplasmsSuccinate DehydrogenaseTranslocation, GeneticTuberous SclerosisTumor Suppressor ProteinsUbiquitin ThiolesteraseBAP1 protein, humanMET protein, humanProto-Oncogene Proteins c-metSuccinate DehydrogenaseTumor Suppressor ProteinsUbiquitin ThiolesteraseBirt-Hogg-Dube diseaseGenetic diseaseGenetic susceptibilityKidney cancervon Hippel Lindau disease

Identifiers

PMID24359990
PMCPMC3872053
OpenAlexW2090960951

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.