Variants in the Kallikrein Gene Family and Hypermobile Ehlers-Danlos Syndrome
- DOI
- 10.21203/rs.3.rs-4547888/v1
- Published
- 2024-06-10
- Container
- Not recorded
- Publisher
- Not recorded
- Open access
- yes
Credibility signals
limited evidence Score 41/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.
Show all credibility signals
- cautionDOI registered: No matching Crossref record was present in this response.
- cautionDOI resolves: No matching Crossref record was present in this response.
- not scoredDirectory of Open Access Journals: No matching DOAJ record was present in this response. No allow-list match; this is not evidence of low credibility.
- not scoredMEDLINE indexed: Not checked or no result supplied; no credibility inference made.
- not scoredOpenAlex core source: Not checked or no result supplied; no credibility inference made.
- not scoredKnown publisher allow-list: Not checked or no result supplied; no credibility inference made.
- not scoredROR affiliation: Not checked or no result supplied; no credibility inference made.
- not scoredRetraction Watch retraction: No retraction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredRetraction Watch expression of concern: No expression of concern notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredRetraction Watch correction: No correction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredRetraction Watch reinstatement: No reinstatement notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- supportingOpen access status: Normalized open-access status: open.
- not scoredPublication license: Not checked or no result supplied; no credibility inference made.
- cautionPublication version: Identified as a preprint; peer review and later versions may change the record.
- cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty.
Cite this work
BibTeX
@article{allodium:10.21203/rs.3.rs-4547888/v1,
title = {Variants in the Kallikrein Gene Family and Hypermobile Ehlers-Danlos Syndrome},
author = {Gensemer C and Beck T and Guo L and Petrucci T and Morningstar J and Kornblau I and Byerly K and Biggs R and Weintraub A and Moore K and Koren N and Daylor V and Hastings C and Oberlies E and Zientara ER and Devey E and Dooley S and Stayer K and Fenner R and Singleton K and Luzbetak S and Bear D and Byrd R and Weninger J and Bistran E and Beeson G and Kerns J and Griggs M and Griggs C and Osterhaus M and Fleck E and Schnaudigel J and Butler S and Severance S and Kendall W and Delaney JR and Judge DP and Chen P and Yao H and Guz J and Awgulewitsch A and Kautz SA and Mukherjee R and Price R and Henderson F and Shapiro S and Francomano CA and Kovacic JC and Lavallee M and Patel S and Berrandou T and Slaugenhaupt SA and Milan D and Kontorovich AR and Bouatia-Naji N and Norris RA.},
year = {2024},
doi = {10.21203/rs.3.rs-4547888/v1},
url = {https://doi.org/10.21203/rs.3.rs-4547888/v1}
}RIS
TY - JOUR TI - Variants in the Kallikrein Gene Family and Hypermobile Ehlers-Danlos Syndrome AU - Gensemer C AU - Beck T AU - Guo L AU - Petrucci T AU - Morningstar J AU - Kornblau I AU - Byerly K AU - Biggs R AU - Weintraub A AU - Moore K AU - Koren N AU - Daylor V AU - Hastings C AU - Oberlies E AU - Zientara ER AU - Devey E AU - Dooley S AU - Stayer K AU - Fenner R AU - Singleton K AU - Luzbetak S AU - Bear D AU - Byrd R AU - Weninger J AU - Bistran E AU - Beeson G AU - Kerns J AU - Griggs M AU - Griggs C AU - Osterhaus M AU - Fleck E AU - Schnaudigel J AU - Butler S AU - Severance S AU - Kendall W AU - Delaney JR AU - Judge DP AU - Chen P AU - Yao H AU - Guz J AU - Awgulewitsch A AU - Kautz SA AU - Mukherjee R AU - Price R AU - Henderson F AU - Shapiro S AU - Francomano CA AU - Kovacic JC AU - Lavallee M AU - Patel S AU - Berrandou T AU - Slaugenhaupt SA AU - Milan D AU - Kontorovich AR AU - Bouatia-Naji N AU - Norris RA. PY - 2024 DO - 10.21203/rs.3.rs-4547888/v1 UR - https://doi.org/10.21203/rs.3.rs-4547888/v1 ER -
APA
C, G., T, B., L, G., T, P., J, M., I, K., K, B., R, B., A, W., K, M., N, K., V, D., C, H., E, O., ER, Z., E, D., S, D., K, S., R, F., K, S., S, L., D, B., R, B., J, W., E, B., G, B., J, K., M, G., C, G., M, O., E, F., J, S., S, B., S, S., W, K., JR, D., DP, J., P, C., H, Y., J, G., A, A., SA, K., R, M., R, P., F, H., S, S., CA, F., JC, K., M, L., S, P., T, B., SA, S., D, M., AR, K., N, B., & RA., N. (2024). Variants in the Kallikrein Gene Family and Hypermobile Ehlers-Danlos Syndrome. https://doi.org/10.21203/rs.3.rs-4547888/v1
Source records
- europe-pmc · retrieved 2026-11-10T14:05:03.219Z
- hal · retrieved 2026-11-10T14:05:03.265Z