Class information for:
Level 1: SHOX//LERI WEILL DYSCHONDROSTEOSIS//SHOX GENE

Basic class information
Class id #P Avg. number of
references		 Database coverage
of references
22902 365 26.8 72%


Bar chart of Publication_year

Last years might be incomplete

Hierarchy of classes
The table includes all classes above and classes immediately below the current class.


Cluster id Level Cluster label #P
0 4 BIOCHEMISTRY & MOLECULAR BIOLOGY//CELL BIOLOGY//ONCOLOGY 4064930
196 3       GENETICS & HEREDITY//FRAGILE X SYNDROME//AMERICAN JOURNAL OF MEDICAL GENETICS 53756
898 2             TURNER SYNDROME//KLINEFELTER SYNDROME//PREMATURE OVARIAN FAILURE 11325
22902 1                   SHOX//LERI WEILL DYSCHONDROSTEOSIS//SHOX GENE 365

Terms with highest relevance score


rank Term termType Chi square Shr. of publ. in
class containing
term		 Class's shr. of
term's tot. occurrences		 #P with
term in
class
1 SHOX authKW 3419767 15% 74% 55
2 LERI WEILL DYSCHONDROSTEOSIS authKW 2844365 9% 100% 34
3 SHOX GENE authKW 1802963 7% 86% 25
4 MADELUNG DEFORMITY authKW 1639066 6% 85% 23
5 LERI WEILL SYNDROME authKW 1505840 5% 100% 18
6 MADELUNGS DEFORMITY authKW 1355253 5% 90% 18
7 DYSCHONDROSTEOSIS authKW 803110 3% 80% 12
8 LANGER MESOMELIC DYSPLASIA authKW 752920 2% 100% 9
9 MADELUNG authKW 464757 3% 56% 10
10 SHOX DEFICIENCY authKW 430238 2% 86% 6

Web of Science journal categories


Rank Term Chi square Shr. of publ. in
class containing
term		 Class's shr. of
term's tot. occurrences		 #P with
term in
class
1 Genetics & Heredity 3960 43% 0% 158
2 Endocrinology & Metabolism 832 19% 0% 70
3 Orthopedics 746 13% 0% 46
4 Pediatrics 711 16% 0% 58
5 Surgery 128 12% 0% 44
6 Developmental Biology 63 3% 0% 11
7 Medical Ethics 25 1% 0% 2
8 Radiology, Nuclear Medicine & Medical Imaging 19 4% 0% 15
9 Reproductive Biology 16 2% 0% 6
10 Archaeology 15 1% 0% 3

Address terms


Rank Term Chi square Shr. of publ. in
class containing
term		 Class's shr. of
term's tot. occurrences		 #P with
term in
class
1 CHCG DIAGNOST GENOME ANAL 167316 1% 100% 2
2 DERMOTT HUMAN GROWTH DEV 167316 1% 100% 2
3 DIPARTIMENTO PEDIAT GINECOL 167316 1% 100% 2
4 ROYAL CHILDRENS HOSP FDN 111542 1% 67% 2
5 MED MOL GENET INGEMM 91253 2% 18% 6
6 ADULT AUTISM SPE UM ADHD SERV 83658 0% 100% 1
7 ADV PEDIAT MED 83658 0% 100% 1
8 ASS CANTE MONTEVECCHIO 83658 0% 100% 1
9 BEHAV DEV PSYCHIAT 83658 0% 100% 1
10 BIOMED SCI AGING 83658 0% 100% 1

Journals


Rank Term Chi square Shr. of publ. in
class containing
term		 Class's shr. of
term's tot. occurrences		 #P with
term in
class
1 HORMONE RESEARCH IN PAEDIATRICS 19872 4% 2% 14
2 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 6380 6% 0% 21
3 JOURNAL OF MEDICAL GENETICS 4162 5% 0% 17
4 AMERICAN JOURNAL OF MEDICAL GENETICS 3432 5% 0% 19
5 JOURNAL OF HAND SURGERY-AMERICAN VOLUME 2929 4% 0% 16
6 HUMAN GENETICS 2671 4% 0% 16
7 JOURNAL OF HAND SURGERY-BRITISH AND EUROPEAN VOLUME 2604 3% 0% 10
8 JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM 2332 3% 0% 10
9 JOURNAL OF PEDIATRIC ORTHOPAEDICS-PART B 1623 2% 0% 6
10 MOLECULAR CYTOGENETICS 1546 1% 1% 3

Author Key Words


Rank Term Chi square Shr. of publ. in
class containing
term		 Class's shr. of
term's tot. occurrences		 #P with
term in
class		 LCSH search Wikipedia search
1 SHOX 3419767 15% 74% 55 Search SHOX Search SHOX
2 LERI WEILL DYSCHONDROSTEOSIS 2844365 9% 100% 34 Search LERI+WEILL+DYSCHONDROSTEOSIS Search LERI+WEILL+DYSCHONDROSTEOSIS
3 SHOX GENE 1802963 7% 86% 25 Search SHOX+GENE Search SHOX+GENE
4 MADELUNG DEFORMITY 1639066 6% 85% 23 Search MADELUNG+DEFORMITY Search MADELUNG+DEFORMITY
5 LERI WEILL SYNDROME 1505840 5% 100% 18 Search LERI+WEILL+SYNDROME Search LERI+WEILL+SYNDROME
6 MADELUNGS DEFORMITY 1355253 5% 90% 18 Search MADELUNGS+DEFORMITY Search MADELUNGS+DEFORMITY
7 DYSCHONDROSTEOSIS 803110 3% 80% 12 Search DYSCHONDROSTEOSIS Search DYSCHONDROSTEOSIS
8 LANGER MESOMELIC DYSPLASIA 752920 2% 100% 9 Search LANGER+MESOMELIC+DYSPLASIA Search LANGER+MESOMELIC+DYSPLASIA
9 MADELUNG 464757 3% 56% 10 Search MADELUNG Search MADELUNG
10 SHOX DEFICIENCY 430238 2% 86% 6 Search SHOX+DEFICIENCY Search SHOX+DEFICIENCY

Core articles
The table includes core articles in the class. The following variables is taken into account for the relevance score of an article in a cluster c:
(1) Number of references referring to publications in the class.
(2) Share of total number of active references referring to publications in the class.
(3) Age of the article. New articles get higher score than old articles.
(4) Citation rate, normalized to year.


Rank Reference # ref.
in cl.		 Shr. of ref. in
cl.		 Citations
1 GAHUNIA, HK , BABYN, PS , KIRSCH, S , MENDOZA-LONDONO, R , (2009) IMAGING OF SHOX-ASSOCIATED ANOMALIES.SEMINARS IN MUSCULOSKELETAL RADIOLOGY. VOL. 13. ISSUE 3. P. 236-254 53 91% 3
2 MARCHINI, A , OGATA, T , RAPPOLD, GA , (2016) A TRACK RECORD ON SHOX: FROM BASIC RESEARCH TO COMPLEX MODELS AND THERAPY.ENDOCRINE REVIEWS. VOL. 37. ISSUE 4. P. 417 -448 91 44% 0
3 BINDER, G , (2011) SHORT STATURE DUE TO SHOX DEFICIENCY: GENOTYPE, PHENOTYPE, AND THERAPY.HORMONE RESEARCH IN PAEDIATRICS. VOL. 75. ISSUE 2. P. 81-89 36 95% 73
4 BUNYAN, DJ , BAFFICO, M , CAPONE, L , VANNELLI, S , IUGHETTI, L , SCHMITT, S , TAYLOR, EJ , HERRIDGE, AA , SHEARS, D , FORABOSCO, A , ET AL (2016) DUPLICATIONS UPSTREAM AND DOWNSTREAM OF SHOX IDENTIFIED AS NOVEL CAUSES OF LERI-WEILL DYSCHONDROSTEOSIS OR IDIOPATHIC SHORT STATURE.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 170. ISSUE 4. P. 949 -957 27 90% 2
5 GATTA, V , PALKA, C , CHIAVAROLI, V , FRANCHI, S , CANNATARO, G , SAVASTANO, M , COTRONEO, AR , CHIARELLI, F , MOHN, A , STUPPIA, L , (2014) SPECTRUM OF PHENOTYPIC ANOMALIES IN FOUR FAMILIES WITH DELETION OF THE SHOX ENHANCER REGION.BMC MEDICAL GENETICS. VOL. 15. ISSUE . P. - 27 96% 4
6 AUGER, J , BAPTISTE, A , BENABBAD, I , THIERRY, G , COSTA, JM , AMOUYAL, M , KOTTLER, ML , LEHEUP, B , TOURAINE, R , SCHMITT, S , ET AL (2016) GENOTYPE-PHENOTYPE RELATIONSHIP IN PATIENTS AND RELATIVES WITH SHOX REGION ANOMALIES IN THE FRENCH POPULATION.HORMONE RESEARCH IN PAEDIATRICS. VOL. 86. ISSUE 5. P. 309 -318 28 90% 0
7 RODRIGUEZ, FA , UNANUE, N , HERNANDEZ, MI , BASAURE, J , HEATH, KE , CASSORLA, F , (2013) CLINICAL AND MOLECULAR CHARACTERIZATION OF CHILEAN PATIENTS WITH LERI-WEILL DYSCHONDROSTEOSIS.JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM. VOL. 26. ISSUE 7-8. P. 729-734 27 96% 1
8 BENITO-SANZ, S , BELINCHON-MARTINEZ, A , AZA-CARMONA, M , DE LA TORRE, C , HUBER, C , GONZALEZ-CASADO, I , ROSS, JL , THOMAS, NS , ZINN, AR , CORMIER-DAIRE, V , ET AL (2017) IDENTIFICATION OF 15 NOVEL PARTIAL SHOX DELETIONS AND 13 PARTIAL DUPLICATIONS, AND A REVIEW OF THE LITERATURE REVEALS INTRON 3 TO BE A HOTSPOT REGION.JOURNAL OF HUMAN GENETICS. VOL. 62. ISSUE 2. P. 229 -234 28 80% 0
9 RAPPOLD, G , BLUM, WF , SHAVRIKOVA, EP , CROWE, BJ , ROETH, R , QUIGLEY, CA , ROSS, JL , NIESLER, B , (2007) GENOTYPES AND PHENOTYPES IN CHILDREN WITH SHORT STATURE: CLINICAL INDICATORS OF SHOX HAPLOINSUFFICIENCY.JOURNAL OF MEDICAL GENETICS. VOL. 44. ISSUE 5. P. 306-313 27 87% 81
10 BENITO-SANZ, S , BARROSO, E , HEINE-SUNER, D , HISADO-OLIVA, A , ROMANELLI, V , ROSELL, J , ARAGONES, A , CAIMARI, M , ARGENTE, J , ROSS, JL , ET AL (2011) CLINICAL AND MOLECULAR EVALUATION OF SHOX/PAR1 DUPLICATIONS IN LERI-WEILL DYSCHONDROSTEOSIS (LWD) AND IDIOPATHIC SHORT STATURE (ISS).JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM. VOL. 96. ISSUE 2. P. E404 -E412 25 86% 33

Classes with closest relation at Level 1


Rank Class id link
1 16125 CD99//45 X MALE//SEX TEST
2 4013 TURNER SYNDROME//ULLRICH TURNER SYNDROME//X MONOSOMY
3 10084 PREMATURE OVARIAN FAILURE//PRIMARY OVARIAN INSUFFICIENCY//PREMATURE MENOPAUSE
4 12125 STEROID SULFATASE//X LINKED ICHTHYOSIS//ESTRONE SULFATASE
5 20430 PROXIMAL SYMPHALANGISM//SYMPHALANGISM//NOG
6 29212 ZFAT//CENT ADV MOL MED//ZBTB38 GENE
7 26141 47 XYY MALES//TAURODONTISM//ORAL DEV ORTHODONT
8 4324 AZF//Y CHROMOSOME MICRODELETION//Y CHROMOSOME
9 10787 LARON SYNDROME//GROWTH HORMONE INSENSITIVITY//GH 1 GENE
10 32361 PARIETAL FORAMINA//FORAMINA PARIETALIA PERMAGNA//POTOCKI SHAFFER SYNDROME

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