Student or educator? Sign up with your school email and get 6 months of Pro free.
Cited by 946

The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.

Genetic Linkage Evidence for a Familial Alzheimer's Disease Locus on Chromosome 14

Schellenberg, Gerard D., Bird, Thomas D., Wijsman, Ellen M., Orr, Harry T., Anderson, Leojean, Nemens, Ellen, White, June A., Bonnycastle, Lori, Weber, James L., Alonso, M. Elisa, Potter, Huntington, Heston, Leonard L., Martin, George M.·1992·Science

Abstract

Linkage analysis was used to search the genome for chromosomal regions harboring familial Alzheimer's disease genes. Markers on chromosome 14 gave highly significant positive lod scores in early-onset non-Volga German kindreds; a Z max of 9.15 (θ = 0.01) was obtained with the marker D14S43 at 14q24.3. One early-onset family yielded a lod score of 4.89 (θ = 0.0). When no assumptions were made about age-dependent penetrance, significant results were still obtained (Z max = 5.94, θ = 0.0), despite the loss of power to detect linkage under these conditions. Results for the Volga German families were either negative or nonsignificant for markers in this region. Thus, evidence indicates a familial Alzheimer's disease locus on chromosome 14.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1126/science.1411576

Cites

3 of 3 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Show all 3 references

Research works printed but not linked: 51

  1. Bergem, A. L. M., Neurobiology of Aging 13: S66 (1992).
  2. BIRD, T.D., FAMILIAL ALZHEIMERS-DISEASE IN AMERICAN DESCENDANTS OF THE VOLGA GERMANS - PROBABLE GENETIC FOUNDER EFFECT, ANNALS OF NEUROLOGY 23: 25 (1988). · DOI
  3. BIRD, T.D., PHENOTYPIC HETEROGENEITY IN FAMILIAL ALZHEIMERS-DISEASE - A STUDY OF 24 KINDREDS, ANNALS OF NEUROLOGY 25: 12 (1989). · DOI · Paper page
  4. Breitner, J. C. S,, Neurobiology of Aging 13: S66 (1992).
  5. BROWN, I.R., INDUCTION OF HEAT-SHOCK (STRESS) GENES IN THE MAMMALIAN BRAIN BY HYPERTHERMIA AND OTHER TRAUMATIC EVENTS - A CURRENT PERSPECTIVE, JOURNAL OF NEUROSCIENCE RESEARCH 27: 247 (1990). · DOI · Paper page
  6. CHARTIERHARLIN, M.C., SCREENING FOR THE BETA-AMYLOID PRECURSOR PROTEIN MUTATION (APP717-VAL-]ILE) IN EXTENDED PEDIGREES WITH EARLY ONSET ALZHEIMERS-DISEASE, NEUROSCIENCE LETTERS 129: 134 (1991). · DOI
  7. COX, D.W., DNA RESTRICTION FRAGMENTS ASSOCIATED WITH ALPHA-1-ANTITRYPSIN INDICATE A SINGLE ORIGIN FOR DEFICIENCY ALLELE PI Z, NATURE 316: 79 (1985). · DOI · Paper page
  8. CRAWFORD, F, SEQUENCING OF EXONS 16 AND 17 OF THE BETA-AMYLOID PRECURSOR PROTEIN GENE IN 14 FAMILIES WITH EARLY ONSET ALZHEIMERS-DISEASE FAILS TO REVEAL MUTATIONS IN THE BETA-AMYLOID SEQUENCE, NEUROSCIENCE LETTERS 133: 1 (1991). · DOI
  9. DRAGUNOW, M, BRAIN INJURY INDUCES C-FOS PROTEIN(S) IN NERVE AND GLIAL-LIKE CELLS IN ADULT MAMMALIAN BRAIN, BRAIN RESEARCH 455: 295 (1988). · DOI · Paper page
  10. ELLIS, R.J., MOLECULAR CHAPERONES, ANNUAL REVIEW OF BIOCHEMISTRY 60: 321 (1991). · DOI · Paper page
  11. GOUDSMIT, J, FAMILIAL ALZHEIMERS-DISEASE IN 2 KINDREDS OF THE SAME GEOGRAPHIC AND ETHNIC-ORIGIN - A CLINICAL AND GENETIC-STUDY, JOURNAL OF THE NEUROLOGICAL SCIENCES 49: 79 (1981). · DOI
  12. HESTON, L.L., LINKAGE OF AN ALZHEIMER-DISEASE SUSCEPTIBILITY LOCUS TO MARKERS ON HUMAN CHROMOSOME-21, AMERICAN JOURNAL OF MEDICAL GENETICS 40: 449 (1991). · DOI
  13. HODGE, S.E., THE SEARCH FOR HETEROGENEITY IN INSULIN-DEPENDENT DIABETES-MELLITUS (IDDM) - LINKAGE STUDIES, 2-LOCUS MODELS, AND GENETIC-HETEROGENEITY, AMERICAN JOURNAL OF HUMAN GENETICS 35: 1139 (1983).
  14. JORDAN, S. A., NUCLEIC ACIDS RESEARCH 19: 1959 (1959).
  15. KAMINO, K, LINKAGE AND MUTATIONAL ANALYSIS OF FAMILIAL ALZHEIMER-DISEASE KINDREDS FOR THE APP GENE REGION, AMERICAN JOURNAL OF HUMAN GENETICS 51: 998 (1992).
  16. LONG, G.L., COMPLETE SEQUENCE OF THE CDNA FOR HUMAN ALPHA-1-ANTITRYPSIN AND THE GENE FOR THE S-VARIANT, BIOCHEMISTRY 23: 4828 (1984). · DOI · Paper page
  17. MOHS, R.C., ALZHEIMERS-DISEASE - MORBID RISK AMONG 1ST-DEGREE RELATIVES APPROXIMATES 50-PERCENT BY 90 YEARS OF AGE, ARCHIVES OF GENERAL PSYCHIATRY 44: 405 (1987). · DOI
  18. MORTON, N.E., THE DETECTION AND ESTIMATION OF LINKAGE BETWEEN THE GENES FOR ELLIPTOCYTOSIS AND THE RH-BLOOD TYPE, AMERICAN JOURNAL OF HUMAN GENETICS 8: 80 (1956).
  19. 10.1126/science.1925564 · DOI · Paper page
  20. NARUSE, S, MIS-SENSE MUTATION VAL-]ILE IN EXON-17 OF AMYLOID PRECURSOR PROTEIN GENE IN JAPANESE FAMILIAL ALZHEIMERS-DISEASE, LANCET 337: 978 (1991).
  21. NEE, L.E., DEMENTIA OF THE ALZHEIMER TYPE - CLINICAL AND FAMILY STUDY OF 22 TWIN PAIRS, NEUROLOGY 37: 359 (1987). · DOI
  22. NUKIWA, T, CHARACTERIZATION OF THE GENE AND PROTEIN OF THE COMMON ALPHA-L-ANTITRYPSIN NORMAL M2 ALLELE, AMERICAN JOURNAL OF HUMAN GENETICS 43: 322 (1988).
  23. NUKIWA, T, IDENTIFICATION OF A 2ND MUTATION IN THE PROTEIN-CODING SEQUENCE OF THE Z-TYPE ALPHA-1-ANTITRYPSIN GENE, JOURNAL OF BIOLOGICAL CHEMISTRY 261: 15989 (1986). · DOI
  24. PERICAKVANCE, M.A., LINKAGE STUDIES IN FAMILIAL ALZHEIMER-DISEASE - EVIDENCE FOR CHROMOSOME-19 LINKAGE, AMERICAN JOURNAL OF HUMAN GENETICS 48: 1034 (1991).
  25. PERICAKVANCE, M.A., GENETIC-LINKAGE STUDIES IN ALZHEIMERS-DISEASE FAMILIES, EXPERIMENTAL NEUROLOGY 102: 271 (1988). · DOI · Paper page
  26. RAPOPORT, S.I., DISCORDANCE AND CONCORDANCE OF DEMENTIA OF THE ALZHEIMER TYPE (DAT) IN MONOZYGOTIC TWINS INDICATE HERITABLE AND SPORADIC FORMS OF ALZHEIMERS-DISEASE, NEUROLOGY 41: 1549 (1991). · DOI
  27. RISCH, N, A NOTE ON MULTIPLE TESTING PROCEDURES IN LINKAGE ANALYSIS, AMERICAN JOURNAL OF HUMAN GENETICS 48: 1058 (1991).
  28. RUPPERT, C, MOLECULAR BRAIN RESEARCH 2: 51 (1987). · doi:10.1016/0169-328x(87)90020-9
  29. SALBAUM, J.M., THE PROMOTER OF ALZHEIMERS-DISEASE AMYLOID-A4 PRECURSOR GENE, EMBO JOURNAL 7: 2807 (1988). · DOI · Paper page
  30. SCHELLENBERG, G.D., LINKAGE ANALYSIS OF FAMILIAL ALZHEIMER-DISEASE, USING CHROMOSOME-21 MARKERS, AMERICAN JOURNAL OF HUMAN GENETICS 48: 563 (1991).
  31. SCHELLENBERG, G.D., APP717, APP693, AND PRIP GENE-MUTATIONS ARE RARE IN ALZHEIMER-DISEASE, AMERICAN JOURNAL OF HUMAN GENETICS 49: 511 (1991).
  32. SCHELLENBERG, G.D., GENETIC ASSOCIATION AND LINKAGE ANALYSIS OF THE APOLIPOPROTEIN-CII LOCUS AND FAMILIAL ALZHEIMERS-DISEASE, ANNALS OF NEUROLOGY 31: 223 (1992). · DOI
  33. SCHELLENBERG, G. D., NEUROBIOLOGY OF AGING 13 1: S67 (1992).
  34. 10.1126/science.3420406 · DOI · Paper page
  35. SHARMA, V, DINUCLEOTIDE REPEAT POLYMORPHISM AT THE D14S43 LOCUS, NUCLEIC ACIDS RESEARCH 19: 1722 (1991).
  36. SHENG, M, THE REGULATION AND FUNCTION OF C-FOS AND OTHER IMMEDIATE EARLY GENES IN THE NERVOUS-SYSTEM, NEURON 4: 477 (1990).
  37. Smith, C. A. B., Proceedings of the 2nd International Congres on Human Genetics 1: 212 (1961).
  38. STGEORGEHYSLOP, P.H., GENETIC-LINKAGE STUDIES SUGGEST THAT ALZHEIMERS-DISEASE IS NOT A SINGLE HOMOGENEOUS DISORDER, NATURE 347: 194 (1990). · DOI · Paper page
  39. 10.1126/science.2880399 · DOI · Paper page
  40. TANZI, R.E., ASSESSMENT OF AMYLOID BETA-PROTEIN PRECURSOR GENE-MUTATIONS IN A LARGE SET OF FAMILIAL AND SPORADIC ALZHEIMER-DISEASE CASES, AMERICAN JOURNAL OF HUMAN GENETICS 51: 273 (1992).
  41. TANZI, R.E., MOLECULAR-GENETICS OF ALZHEIMER-DISEASE AMYLOID, JOURNAL OF BIOLOGICAL CHEMISTRY 266: 20579 (1991). · DOI
  42. TANZI, R.E., THE GENETIC-DEFECT IN FAMILIAL ALZHEIMERS-DISEASE IS NOT TIGHTLY LINKED TO THE AMYLOID BETA-PROTEIN GENE, NATURE 329: 156 (1987). · DOI · Paper page
  43. VALENCIA, L.G., ALZHEIMER-DISEASE - 7 CASES IN 3 FAMILIES, REVISTA DE INVESTIGACION CLINICA 38: 261 (1986).
  44. VANBROECKHOVEN, C, FAILURE OF FAMILIAL ALZHEIMERS-DISEASE TO SEGREGATE WITH THE A4-AMYLOID GENE IN SEVERAL EUROPEAN FAMILIES, NATURE 329: 153 (1987). · DOI · Paper page
  45. VANDUIJN, C.M., FAMILIAL AGGREGATION OF ALZHEIMERS-DISEASE AND RELATED DISORDERS - A COLLABORATIVE REANALYSIS OF CASE-CONTROL STUDIES, INTERNATIONAL JOURNAL OF EPIDEMIOLOGY 20: S13 (1991). · DOI · Paper page
  46. VANDUIJN, C.M., AMYLOID PRECURSOR PROTEIN GENE MUTATION IN EARLY-ONSET ALZHEIMERS-DISEASE, LANCET 337: 978 (1991).
  47. 10.1016/0888-7543(92)90121-8 · doi:10.1016/0888-7543(92)90121-8
  48. WEITKAMP, L.R., ALZHEIMER-DISEASE - EVIDENCE FOR SUSCEPTIBILITY LOCI ON CHROMOSOME-6 AND CHROMOSOME-14, AMERICAN JOURNAL OF HUMAN GENETICS 35: 443 (1983).
  49. 10.1159/000133727 · doi:10.1159/000133727
  50. YOSHIOKA, K, THE 717VAL-]ILE SUBSTITUTION IN AMYLOID PRECURSOR PROTEIN IS ASSOCIATED WITH FAMILIAL ALZHEIMERS-DISEASE REGARDLESS OF ETHNIC-GROUPS, BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 178: 1141 (1991). · DOI
  51. ZHANG, P, C-FOS PROTEIN-LIKE IMMUNOREACTIVITY - DISTRIBUTION IN THE HUMAN BRAIN AND OVER-EXPRESSION IN THE HIPPOCAMPUS OF PATIENTS WITH ALZHEIMERS-DISEASE, NEUROSCIENCE 46: 9 (1992). · DOI

Cited by

See all 946

Metadata

Authors
Schellenberg, G. D., Bird, T. D., Wijsman, E. M., Orr, H. T., Anderson, L., Nemens, E., White, J. A., Bonnycastle, L., Weber, J. L., Alonso, M. E., Potter, H., Heston, L. L., & Martin, G. M.
Venue
Science
Published
1992-10-23
Volume
258
Issue
5082
Pages
668-671
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W2033356439
Cited by
946
References
3
FWCI
60.93
Type
journal article
Language
en
Open access
closed

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

How to cite

Cite CoChat for the checks on this page, and the paper for its own findings.

This page
CoChat. (2026). Citation check: Genetic Linkage Evidence for a Familial Alzheimer's Disease Locus on Chromosome 14. https://app.cochat.ai/papers/10.1126/science.1411576
The paper
Schellenberg, G. D., Bird, T. D., Wijsman, E. M., Orr, H. T., Anderson, L., Nemens, E., White, J. A., Bonnycastle, L., Weber, J. L., Alonso, M. E., Potter, H., Heston, L. L., & Martin, G. M. (1992). Genetic Linkage Evidence for a Familial Alzheimer's Disease Locus on Chromosome 14. Science. https://doi.org/10.1126/science.1411576

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.