Jörg Schmidtke
Biographic Data
| ID | 7326140 |
|---|---|
| NAME | Jörg Schmidtke |
| GIVEN NAMES | Jörg |
| FAMILY NAME | Schmidtke |
| SIGNATURE | SCHMIDTKE J |
| AFFILIATIONS | Medizinische Hochschule Hannover |
| ORCID | 0000-0001-7739-398X |
| VERIFIED | Yes |
| TOTAL WORKS | 18 |
| TOTAL CITATIONS | 0 |
| AUTHOR COUNT | 18 |
| EDITOR COUNT | 0 |
| FIRST PUBLICATION YEAR | 1993 |
| LATEST PUBLICATION YEAR | 2022 |
| H-INDEX | 0 |
Carrier detection probabilities for autosomal recessive variants in unrelated and consanguineous couples — an evaluation of the 86 genes of the ACMG ‘Tier 3’ panel
Carrier screening for autosomal recessive variants has become a cornerstone of community and public health genetics. While the first carrier screening programs were confined to conditions with relatively high prevalence, and hence well-known carrier frequency, the number of candidate genes has increased greatly since the advent of high-throughput DNA sequencing technologies. The epidemiological database of the ensuing gene panels is mostly sparse…
Genetic studies on the Cayo Santiago rhesus macaques
Genetic studies not only contribute substantially to our current understanding of the natural variation in behavior and health in many species, they also provide the basis of numerous in vivo models of human traits. Despite the many challenges posed by the high level of biological and social complexity, a long lifespan and difficult access in the field, genetic studies of primates are particularly rewarding because of the close evolutionary relat…
Genetic Counseling
Health needs assessment for medical genetic services for congenital disorders in middle- and low-income nations
Cancer risk communication, predictive testing and management in France, Germany, the Netherlands and the UK
Genetic testing has its greatest public health value when it identifies individuals who will benefit from specific interventions based upon their risk. This paradigm is the basis for the use of predictive tests, such as BRCA1/BRCA2 testing which has become part of clinical practice for more than a decade. Currently predictive BRCA1/BRCA2 testing is offered to women using low, moderate and high risk based upon family history as cut-off levels. Non…
Upcoming special issues in the Journal of Community Genetics
Definitions of genetic testing in European legal documents
The wide variation of definitions of genetic testing in international recommendations, guidelines and reports
Funding of rare disease research in Germany
Genetic testing for familial/hereditary breast cancer—comparison of guidelines and recommendations from the UK, France, the Netherlands and Germany
Community genetics. Its definition 2010
This paper presents a definition of the medical field of community genetics. It starts with a brief historical overview, defines the requirements for an adequate definition, presents the definition, and discusses the constituent parts of the definition
Confidence of primary care physicians in their ability to carry out basic medical genetic tasks—a European survey in five countries—Part 1
Points to consider in assessing and appraising predictive genetic tests
The use of predictive genetic tests is expanding rapidly. Given limited health care budgets and few national coverage decisions specifically for genetic tests, evidence of benefits and harms is a key requirement in decision making; however, assessing the benefits and harms of genetic tests raises a number of challenging issues. Frequently, evidence of medical benefits and harms is limited due to practical and ethical limitations of conducting mea…
The journal of community genetics
P~i~nvJc~ sine~sis.Mr Gregory's paper is already i~ ~ype; but owing to its Iength and to delay incidental to preparation of the coloured Plates illustrating it, we have been obliged to hold it over for %he next number of the Journag.~EDD
Scope of definitions of genetic testing
Multiple sirehood in free‐ranging twin rhesus macaques ( Macaca mulatta )
Rhesus macaque females regularly copulate with a number of partners, and produce a single offspring per reproductive cycle in over 99% of cases. We used genotyping of 10 STR markers to determine paternity in the Cayo Santiago population of rhesus macaques. About 1,500 monkeys have been analyzed to date, with their marker genotypes entered into a computerized database. These data enable us to report the first documented case in any cercopithecine …
Male rank, reproductive behavior, and reproductive success in free-ranging rhesus macaques
Power and limits of DNA-profiling in primate populations
No prominent works on this page.
Male rank, reproductive behavior, and reproductive success in free-ranging rhesus macaques
Power and limits of DNA-profiling in primate populations
Multiple sirehood in free‐ranging twin rhesus macaques ( Macaca mulatta )
Rhesus macaque females regularly copulate with a number of partners, and produce a single offspring per reproductive cycle in over 99% of cases. We used genotyping of 10 STR markers to determine paternity in the Cayo Santiago population of rhesus macaques. About 1,500 monkeys have been analyzed to date, with their marker genotypes entered into a computerized database. These data enable us to report the first documented case in any cercopithecine …
Community genetics. Its definition 2010
This paper presents a definition of the medical field of community genetics. It starts with a brief historical overview, defines the requirements for an adequate definition, presents the definition, and discusses the constituent parts of the definition
Confidence of primary care physicians in their ability to carry out basic medical genetic tasks—a European survey in five countries—Part 1
Points to consider in assessing and appraising predictive genetic tests
The use of predictive genetic tests is expanding rapidly. Given limited health care budgets and few national coverage decisions specifically for genetic tests, evidence of benefits and harms is a key requirement in decision making; however, assessing the benefits and harms of genetic tests raises a number of challenging issues. Frequently, evidence of medical benefits and harms is limited due to practical and ethical limitations of conducting mea…
The journal of community genetics
P~i~nvJc~ sine~sis.Mr Gregory's paper is already i~ ~ype; but owing to its Iength and to delay incidental to preparation of the coloured Plates illustrating it, we have been obliged to hold it over for %he next number of the Journag.~EDD
Scope of definitions of genetic testing
Funding of rare disease research in Germany
Genetic testing for familial/hereditary breast cancer—comparison of guidelines and recommendations from the UK, France, the Netherlands and Germany
Upcoming special issues in the Journal of Community Genetics
Definitions of genetic testing in European legal documents
The wide variation of definitions of genetic testing in international recommendations, guidelines and reports
Health needs assessment for medical genetic services for congenital disorders in middle- and low-income nations
Cancer risk communication, predictive testing and management in France, Germany, the Netherlands and the UK
Genetic testing has its greatest public health value when it identifies individuals who will benefit from specific interventions based upon their risk. This paradigm is the basis for the use of predictive tests, such as BRCA1/BRCA2 testing which has become part of clinical practice for more than a decade. Currently predictive BRCA1/BRCA2 testing is offered to women using low, moderate and high risk based upon family history as cut-off levels. Non…
Genetic Counseling
Genetic studies on the Cayo Santiago rhesus macaques
Genetic studies not only contribute substantially to our current understanding of the natural variation in behavior and health in many species, they also provide the basis of numerous in vivo models of human traits. Despite the many challenges posed by the high level of biological and social complexity, a long lifespan and difficult access in the field, genetic studies of primates are particularly rewarding because of the close evolutionary relat…
Carrier detection probabilities for autosomal recessive variants in unrelated and consanguineous couples — an evaluation of the 86 genes of the ACMG ‘Tier 3’ panel
Carrier screening for autosomal recessive variants has become a cornerstone of community and public health genetics. While the first carrier screening programs were confined to conditions with relatively high prevalence, and hence well-known carrier frequency, the number of candidate genes has increased greatly since the advent of high-throughput DNA sequencing technologies. The epidemiological database of the ensuing gene panels is mostly sparse…
Medicine (14 works) · Biology (12 works) · BRCA gene mutations in cancer (12 works) · Genetics (9 works) · Public health (8 works) · Pathology (7 works) · Population (7 works) · Demography (6 works) · Genetic testing (6 works) · Epidemiology (5 works)