Get quick answers to your questions about the article from our AI researcher chatbot
{'id': 'https://openalex.org/W2061432716', 'doi': 'https://doi.org/10.1007/bf00295659', 'title': 'Genetic linkage heterogeneity in the fragile X syndrome', 'display_name': 'Genetic linkage heterogeneity in the fragile X syndrome', 'publication_year': 1985, 'publication_date': '1985-09-01', 'ids': {'openalex': 'https://openalex.org/W2061432716', 'doi': 'https://doi.org/10.1007/bf00295659', 'mag': '2061432716', 'pmid': 'https://pubmed.ncbi.nlm.nih.gov/2993154'}, 'language': 'en', 'primary_location': {'is_oa': False, 'landing_page_url': 'https://doi.org/10.1007/bf00295659', 'pdf_url': None, 'source': {'id': 'https://openalex.org/S199832308', 'display_name': 'Human Genetics', 'issn_l': '0340-6717', 'issn': ['0340-6717', '1432-1203'], 'is_oa': False, 'is_in_doaj': False, 'is_core': True, 'host_organization': 'https://openalex.org/P4310319900', 'host_organization_name': 'Springer Science+Business Media', 'host_organization_lineage': ['https://openalex.org/P4310319965', 'https://openalex.org/P4310319900'], 'host_organization_lineage_names': ['Springer Nature', 'Springer Science+Business Media'], 'type': 'journal'}, 'license': None, 'license_id': None, 'version': None, 'is_accepted': False, 'is_published': False}, 'type': 'article', 'type_crossref': 'journal-article', 'indexed_in': ['crossref', 'pubmed'], 'open_access': {'is_oa': False, 'oa_status': 'closed', 'oa_url': None, 'any_repository_has_fulltext': False}, 'authorships': [{'author_position': 'first', 'author': {'id': 'https://openalex.org/A5090546022', 'display_name': 'W. Ted Brown', 'orcid': None}, 'institutions': [{'id': 'https://openalex.org/I52099693', 'display_name': 'University of York', 'ror': 'https://ror.org/04m01e293', 'country_code': 'GB', 'type': 'education', 'lineage': ['https://openalex.org/I52099693']}], 'countries': ['GB'], 'is_corresponding': False, 'raw_author_name': 'W. T. Brown', 'raw_affiliation_strings': ['Institute for Basic Research in Developmental Disabilities, New York State Office of Mental Retardation and Developmental Disabilities, Staten Island, USA.'], 'affiliations': [{'raw_affiliation_string': 'Institute for Basic Research in Developmental Disabilities, New York State Office of Mental Retardation and Developmental Disabilities, Staten Island, USA.', 'institution_ids': ['https://openalex.org/I52099693']}]}, {'author_position': 'middle', 'author': {'id': 'https://openalex.org/A5103475426', 'display_name': 'Anne C. Gross', 'orcid': None}, 'institutions': [{'id': 'https://openalex.org/I52099693', 'display_name': 'University of York', 'ror': 'https://ror.org/04m01e293', 'country_code': 'GB', 'type': 'education', 'lineage': ['https://openalex.org/I52099693']}], 'countries': ['GB'], 'is_corresponding': False, 'raw_author_name': 'Anne C. Gross', 'raw_affiliation_strings': ['Institute for Basic Research in Developmental Disabilities, New York State Office of Mental Retardation and Developmental Disabilities, Staten Island, USA.'], 'affiliations': [{'raw_affiliation_string': 'Institute for Basic Research in Developmental Disabilities, New York State Office of Mental Retardation and Developmental Disabilities, Staten Island, USA.', 'institution_ids': ['https://openalex.org/I52099693']}]}, {'author_position': 'middle', 'author': {'id': 'https://openalex.org/A5068303186', 'display_name': 'ColinB. Chan', 'orcid': None}, 'institutions': [{'id': 'https://openalex.org/I52099693', 'display_name': 'University of York', 'ror': 'https://ror.org/04m01e293', 'country_code': 'GB', 'type': 'education', 'lineage': ['https://openalex.org/I52099693']}], 'countries': ['GB'], 'is_corresponding': False, 'raw_author_name': 'C. B. Chan', 'raw_affiliation_strings': ['Institute for Basic Research in Developmental Disabilities, New York State Office of Mental Retardation and Developmental Disabilities, Staten Island, USA.'], 'affiliations': [{'raw_affiliation_string': 'Institute for Basic Research in Developmental Disabilities, New York State Office of Mental Retardation and Developmental Disabilities, Staten Island, USA.', 'institution_ids': ['https://openalex.org/I52099693']}]}, {'author_position': 'last', 'author': {'id': 'https://openalex.org/A5043624782', 'display_name': 'Edmund C. Jenkins', 'orcid': 'https://orcid.org/0000-0003-1982-7465'}, 'institutions': [{'id': 'https://openalex.org/I52099693', 'display_name': 'University of York', 'ror': 'https://ror.org/04m01e293', 'country_code': 'GB', 'type': 'education', 'lineage': ['https://openalex.org/I52099693']}], 'countries': ['GB'], 'is_corresponding': False, 'raw_author_name': 'E. C. Jenkins', 'raw_affiliation_strings': ['Institute for Basic Research in Developmental Disabilities, New York State Office of Mental Retardation and Developmental Disabilities, Staten Island, USA.'], 'affiliations': [{'raw_affiliation_string': 'Institute for Basic Research in Developmental Disabilities, New York State Office of Mental Retardation and Developmental Disabilities, Staten Island, USA.', 'institution_ids': ['https://openalex.org/I52099693']}]}], 'institution_assertions': [], 'countries_distinct_count': 1, 'institutions_distinct_count': 1, 'corresponding_author_ids': [], 'corresponding_institution_ids': [], 'apc_list': {'value': 3790, 'currency': 'EUR', 'value_usd': 4690, 'provenance': 'doaj'}, 'apc_paid': None, 'fwci': 9.894, 'has_fulltext': True, 'fulltext_origin': 'ngrams', 'cited_by_count': 59, 'citation_normalized_percentile': {'value': 0.679219, 'is_in_top_1_percent': False, 'is_in_top_10_percent': False}, 'cited_by_percentile_year': {'min': 94, 'max': 95}, 'biblio': {'volume': '71', 'issue': '1', 'first_page': '11', 'last_page': '18'}, 'is_retracted': False, 'is_paratext': False, 'primary_topic': {'id': 'https://openalex.org/T11772', 'display_name': 'Molecular Basis of Rett Syndrome and Related Disorders', 'score': 0.9999, 'subfield': {'id': 'https://openalex.org/subfields/1311', 'display_name': 'Genetics'}, 'field': {'id': 'https://openalex.org/fields/13', 'display_name': 'Biochemistry, Genetics and Molecular Biology'}, 'domain': {'id': 'https://openalex.org/domains/1', 'display_name': 'Life Sciences'}}, 'topics': [{'id': 'https://openalex.org/T11772', 'display_name': 'Molecular Basis of Rett Syndrome and Related Disorders', 'score': 0.9999, 'subfield': {'id': 'https://openalex.org/subfields/1311', 'display_name': 'Genetics'}, 'field': {'id': 'https://openalex.org/fields/13', 'display_name': 'Biochemistry, Genetics and Molecular Biology'}, 'domain': {'id': 'https://openalex.org/domains/1', 'display_name': 'Life Sciences'}}, {'id': 'https://openalex.org/T10269', 'display_name': 'Epigenetic Modifications and Their Functional Implications', 'score': 0.944, 'subfield': {'id': 'https://openalex.org/subfields/1312', 'display_name': 'Molecular Biology'}, 'field': {'id': 'https://openalex.org/fields/13', 'display_name': 'Biochemistry, Genetics and Molecular Biology'}, 'domain': {'id': 'https://openalex.org/domains/1', 'display_name': 'Life Sciences'}}, {'id': 'https://openalex.org/T10106', 'display_name': 'Autism Spectrum Disorders', 'score': 0.9386, 'subfield': {'id': 'https://openalex.org/subfields/2805', 'display_name': 'Cognitive Neuroscience'}, 'field': {'id': 'https://openalex.org/fields/28', 'display_name': 'Neuroscience'}, 'domain': {'id': 'https://openalex.org/domains/1', 'display_name': 'Life Sciences'}}], 'keywords': [{'id': 'https://openalex.org/keywords/pedigree-chart', 'display_name': 'Pedigree chart', 'score': 0.9713397}, {'id': 'https://openalex.org/keywords/genetic-linkage', 'display_name': 'Genetic linkage', 'score': 0.7205778}, {'id': 'https://openalex.org/keywords/penetrance', 'display_name': 'Penetrance', 'score': 0.7122822}, {'id': 'https://openalex.org/keywords/lod-score', 'display_name': 'Lod score', 'score': 0.678022}, {'id': 'https://openalex.org/keywords/linkage', 'display_name': 'Linkage (software)', 'score': 0.66364723}, {'id': 'https://openalex.org/keywords/recombination-fraction', 'display_name': 'Recombination Fraction', 'score': 0.6554902}, {'id': 'https://openalex.org/keywords/fragile-x-syndrome', 'display_name': 'Fragile X Syndrome', 'score': 0.541723}], 'concepts': [{'id': 'https://openalex.org/C22593422', 'wikidata': 'https://www.wikidata.org/wiki/Q3242583', 'display_name': 'Pedigree chart', 'level': 3, 'score': 0.9713397}, {'id': 'https://openalex.org/C54355233', 'wikidata': 'https://www.wikidata.org/wiki/Q7162', 'display_name': 'Genetics', 'level': 1, 'score': 0.7270954}, {'id': 'https://openalex.org/C142870003', 'wikidata': 'https://www.wikidata.org/wiki/Q843863', 'display_name': 'Genetic linkage', 'level': 3, 'score': 0.7205778}, {'id': 'https://openalex.org/C86803240', 'wikidata': 'https://www.wikidata.org/wiki/Q420', 'display_name': 'Biology', 'level': 0, 'score': 0.7166909}, {'id': 'https://openalex.org/C200544954', 'wikidata': 'https://www.wikidata.org/wiki/Q516389', 'display_name': 'Penetrance', 'level': 4, 'score': 0.7122822}, {'id': 'https://openalex.org/C2993098900', 'wikidata': 'https://www.wikidata.org/wiki/Q843863', 'display_name': 'Lod score', 'level': 5, 'score': 0.678022}, {'id': 'https://openalex.org/C31266012', 'wikidata': 'https://www.wikidata.org/wiki/Q6554340', 'display_name': 'Linkage (software)', 'level': 3, 'score': 0.66364723}, {'id': 'https://openalex.org/C2910653347', 'wikidata': 'https://www.wikidata.org/wiki/Q843863', 'display_name': 'Recombination Fraction', 'level': 5, 'score': 0.6554902}, {'id': 'https://openalex.org/C168007829', 'wikidata': 'https://www.wikidata.org/wiki/Q857299', 'display_name': 'Restriction fragment length polymorphism', 'level': 4, 'score': 0.57357836}, {'id': 'https://openalex.org/C2777630245', 'wikidata': 'https://www.wikidata.org/wiki/Q221472', 'display_name': 'Fragile X syndrome', 'level': 2, 'score': 0.54809505}, {'id': 'https://openalex.org/C190789776', 'wikidata': 'https://www.wikidata.org/wiki/Q767511', 'display_name': 'Genetic marker', 'level': 3, 'score': 0.47929993}, {'id': 'https://openalex.org/C64618202', 'wikidata': 'https://www.wikidata.org/wiki/Q3733697', 'display_name': 'Genetic heterogeneity', 'level': 4, 'score': 0.43816483}, {'id': 'https://openalex.org/C122735190', 'wikidata': 'https://www.wikidata.org/wiki/Q715789', 'display_name': 'Gene mapping', 'level': 4, 'score': 0.3625554}, {'id': 'https://openalex.org/C30481170', 'wikidata': 'https://www.wikidata.org/wiki/Q37748', 'display_name': 'Chromosome', 'level': 3, 'score': 0.30607414}, {'id': 'https://openalex.org/C135763542', 'wikidata': 'https://www.wikidata.org/wiki/Q106016', 'display_name': 'Genotype', 'level': 3, 'score': 0.19036514}, {'id': 'https://openalex.org/C104317684', 'wikidata': 'https://www.wikidata.org/wiki/Q7187', 'display_name': 'Gene', 'level': 2, 'score': 0.12242499}, {'id': 'https://openalex.org/C127716648', 'wikidata': 'https://www.wikidata.org/wiki/Q104053', 'display_name': 'Phenotype', 'level': 3, 'score': 0.0}], 'mesh': [{'descriptor_ui': 'D015252', 'descriptor_name': 'Deoxyribonucleases, Type II Site-Specific', 'qualifier_ui': '', 'qualifier_name': None, 'is_major_topic': True}, {'descriptor_ui': 'D005600', 'descriptor_name': 'Fragile X Syndrome', 'qualifier_ui': 'Q000235', 'qualifier_name': 'genetics', 'is_major_topic': True}, {'descriptor_ui': 'D008040', 'descriptor_name': 'Genetic Linkage', 'qualifier_ui': '', 'qualifier_name': None, 'is_major_topic': True}, {'descriptor_ui': 'D014644', 'descriptor_name': 'Genetic Variation', 'qualifier_ui': '', 'qualifier_name': None, 'is_major_topic': True}, {'descriptor_ui': 'D012729', 'descriptor_name': 'Sex Chromosome Aberrations', 'qualifier_ui': 'Q000235', 'qualifier_name': 'genetics', 'is_major_topic': True}, {'descriptor_ui': 'D000293', 'descriptor_name': 'Adolescent', 'qualifier_ui': '', 'qualifier_name': None, 'is_major_topic': False}, {'descriptor_ui': 'D000328', 'descriptor_name': 'Adult', 'qualifier_ui': '', 'qualifier_name': None, 'is_major_topic': False}, {'descriptor_ui': 'D002648', 'descriptor_name': 'Child', 'qualifier_ui': '', 'qualifier_name': None, 'is_major_topic': False}, {'descriptor_ui': 'D004262', 'descriptor_name': 'DNA Restriction Enzymes', 'qualifier_ui': '', 'qualifier_name': None, 'is_major_topic': False}, {'descriptor_ui': 'D005164', 'descriptor_name': 'Factor IX', 'qualifier_ui': 'Q000235', 'qualifier_name': 'genetics', 'is_major_topic': False}, {'descriptor_ui': 'D005164', 'descriptor_name': 'Factor IX', 'qualifier_ui': '', 'qualifier_name': None, 'is_major_topic': False}, {'descriptor_ui': 'D005260', 'descriptor_name': 'Female', 'qualifier_ui': '', 'qualifier_name': None, 'is_major_topic': False}, {'descriptor_ui': 'D005600', 'descriptor_name': 'Fragile X Syndrome', 'qualifier_ui': '', 'qualifier_name': None, 'is_major_topic': False}, {'descriptor_ui': 'D005819', 'descriptor_name': 'Genetic Markers', 'qualifier_ui': '', 'qualifier_name': None, 'is_major_topic': False}, {'descriptor_ui': 'D006801', 'descriptor_name': 'Humans', 'qualifier_ui': '', 'qualifier_name': None, 'is_major_topic': False}, {'descriptor_ui': 'D008297', 'descriptor_name': 'Male', 'qualifier_ui': '', 'qualifier_name': None, 'is_major_topic': False}, {'descriptor_ui': 'D010375', 'descriptor_name': 'Pedigree', 'qualifier_ui': '', 'qualifier_name': None, 'is_major_topic': False}, {'descriptor_ui': 'D011110', 'descriptor_name': 'Polymorphism, Genetic', 'qualifier_ui': '', 'qualifier_name': None, 'is_major_topic': False}, {'descriptor_ui': 'D012729', 'descriptor_name': 'Sex Chromosome Aberrations', 'qualifier_ui': '', 'qualifier_name': None, 'is_major_topic': False}], 'locations_count': 2, 'locations': [{'is_oa': False, 'landing_page_url': 'https://doi.org/10.1007/bf00295659', 'pdf_url': None, 'source': {'id': 'https://openalex.org/S199832308', 'display_name': 'Human Genetics', 'issn_l': '0340-6717', 'issn': ['0340-6717', '1432-1203'], 'is_oa': False, 'is_in_doaj': False, 'is_core': True, 'host_organization': 'https://openalex.org/P4310319900', 'host_organization_name': 'Springer Science+Business Media', 'host_organization_lineage': ['https://openalex.org/P4310319965', 'https://openalex.org/P4310319900'], 'host_organization_lineage_names': ['Springer Nature', 'Springer Science+Business Media'], 'type': 'journal'}, 'license': None, 'license_id': None, 'version': None, 'is_accepted': False, 'is_published': False}, {'is_oa': False, 'landing_page_url': 'https://pubmed.ncbi.nlm.nih.gov/2993154', 'pdf_url': None, 'source': {'id': 'https://openalex.org/S4306525036', 'display_name': 'PubMed', 'issn_l': None, 'issn': None, 'is_oa': False, 'is_in_doaj': False, 'is_core': False, 'host_organization': 'https://openalex.org/I1299303238', 'host_organization_name': 'National Institutes of Health', 'host_organization_lineage': ['https://openalex.org/I1299303238'], 'host_organization_lineage_names': ['National Institutes of Health'], 'type': 'repository'}, 'license': None, 'license_id': None, 'version': None, 'is_accepted': False, 'is_published': False}], 'best_oa_location': None, 'sustainable_development_goals': [], 'grants': [], 'datasets': [], 'versions': [], 'referenced_works_count': 42, 'referenced_works': ['https://openalex.org/W1604929717', 'https://openalex.org/W1964533621', 'https://openalex.org/W1969056887', 'https://openalex.org/W1972322732', 'https://openalex.org/W1972418255', 'https://openalex.org/W1975147643', 'https://openalex.org/W1977923965', 'https://openalex.org/W1978589660', 'https://openalex.org/W1982439021', 'https://openalex.org/W1989432434', 'https://openalex.org/W1989601612', 'https://openalex.org/W1993017405', 'https://openalex.org/W1993130120', 'https://openalex.org/W1997557106', 'https://openalex.org/W1998285142', 'https://openalex.org/W1998537613', 'https://openalex.org/W2008992278', 'https://openalex.org/W2013991104', 'https://openalex.org/W2014119996', 'https://openalex.org/W2019435196', 'https://openalex.org/W2024152203', 'https://openalex.org/W2024640960', 'https://openalex.org/W2030422401', 'https://openalex.org/W2032124694', 'https://openalex.org/W2033591452', 'https://openalex.org/W2045927661', 'https://openalex.org/W2046530033', 'https://openalex.org/W2055092110', 'https://openalex.org/W2056886670', 'https://openalex.org/W2063450941', 'https://openalex.org/W2064947206', 'https://openalex.org/W2074226874', 'https://openalex.org/W2081099466', 'https://openalex.org/W2091760145', 'https://openalex.org/W2122254636', 'https://openalex.org/W2125853201', 'https://openalex.org/W2126287482', 'https://openalex.org/W2402091794', 'https://openalex.org/W2416618226', 'https://openalex.org/W2796338337', 'https://openalex.org/W327692510', 'https://openalex.org/W4290685491'], 'related_works': ['https://openalex.org/W327692510', 'https://openalex.org/W2741033989', 'https://openalex.org/W2159685403', 'https://openalex.org/W2124799131', 'https://openalex.org/W2061432716', 'https://openalex.org/W2045927661', 'https://openalex.org/W1643869946', 'https://openalex.org/W1570882498', 'https://openalex.org/W1506763946', 'https://openalex.org/W1483448916'], 'abstract_inverted_index': None, 'cited_by_api_url': 'https://api.openalex.org/works?filter=cites:W2061432716', 'counts_by_year': [], 'updated_date': '2024-09-19T01:36:58.053179', 'created_date': '2016-06-24'}