Class information for:
Level 1: MULIBREY NANISM//3 M SYNDROME//TRIM37

Basic class information
Class id #P Avg. number of
references		 Database coverage
of references
34066 116 28.0 79%


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
204 3       PROTEASOME//UBIQUITIN//UNFOLDED PROTEIN RESPONSE 52492
677 2             PROTEASOME//UBIQUITIN//PROTEASOME INHIBITOR 13186
34066 1                   MULIBREY NANISM//3 M SYNDROME//TRIM37 116

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 MULIBREY NANISM authKW 3484027 13% 88% 15
2 3 M SYNDROME authKW 3439640 12% 93% 14
3 TRIM37 authKW 2369141 8% 100% 9
4 CUL7 authKW 1938385 8% 82% 9
5 OBSL1 authKW 1316189 4% 100% 5
6 CULLIN7 authKW 1052952 3% 100% 4
7 FBXW8 authKW 701965 3% 67% 4
8 SILVER RUSSEL SYNDROME authKW 350983 2% 67% 2
9 AMBULANT DEFECTS LOCOMOTOR address 263238 1% 100% 1
10 CU17 authKW 263238 1% 100% 1

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 867 36% 0% 42
2 Pediatrics 166 14% 0% 16
3 Cell Biology 110 17% 0% 20
4 Endocrinology & Metabolism 81 11% 0% 13
5 Biochemistry & Molecular Biology 80 25% 0% 29
6 Oncology 37 11% 0% 13
7 Biophysics 22 6% 0% 7
8 Developmental Biology 14 3% 0% 3
9 Pathology 11 3% 0% 4
10 Obstetrics & Gynecology 9 3% 0% 4

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 AMBULANT DEFECTS LOCOMOTOR 263238 1% 100% 1
2 GENET DEV COCHINUMR 8104 263238 1% 100% 1
3 HM MARSEILLEUF 2681 2683 263238 1% 100% 1
4 HMINSERM PHARM 263238 1% 100% 1
5 HOP CONCEPT BIOCHIM BIOL MOL 263238 1% 100% 1
6 HPHOP NECKER ENFANTS MALAD 263238 1% 100% 1
7 MANCHESTER BIOMED BIOMED 263238 1% 100% 1
8 ONCOL AFFILIATED HOSP 263238 1% 100% 1
9 OURCE BRANCH BRAIN DIS BIO OURCE BASED R 263238 1% 100% 1
10 PAEDIAT GENET MOL MED 263238 1% 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 CLINICAL DYSMORPHOLOGY 8495 5% 1% 6
2 JOURNAL OF MEDICAL GENETICS 2225 6% 0% 7
3 ONCOLOGY RESEARCH 1972 3% 0% 3
4 ENDOCRINE CONNECTIONS 1719 1% 1% 1
5 CLINICAL EPIGENETICS 646 1% 0% 1
6 HELVETICA PAEDIATRICA ACTA 553 1% 0% 1
7 AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS 543 1% 0% 1
8 AMERICAN JOURNAL OF HUMAN GENETICS 519 3% 0% 4
9 JOURNAL OF MOLECULAR ENDOCRINOLOGY 501 2% 0% 2
10 AMERICAN JOURNAL OF MEDICAL GENETICS 476 3% 0% 4

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 MULIBREY NANISM 3484027 13% 88% 15 Search MULIBREY+NANISM Search MULIBREY+NANISM
2 3 M SYNDROME 3439640 12% 93% 14 Search 3+M+SYNDROME Search 3+M+SYNDROME
3 TRIM37 2369141 8% 100% 9 Search TRIM37 Search TRIM37
4 CUL7 1938385 8% 82% 9 Search CUL7 Search CUL7
5 OBSL1 1316189 4% 100% 5 Search OBSL1 Search OBSL1
6 CULLIN7 1052952 3% 100% 4 Search CULLIN7 Search CULLIN7
7 FBXW8 701965 3% 67% 4 Search FBXW8 Search FBXW8
8 SILVER RUSSEL SYNDROME 350983 2% 67% 2 Search SILVER+RUSSEL+SYNDROME Search SILVER+RUSSEL+SYNDROME
9 CU17 263238 1% 100% 1 Search CU17 Search CU17
10 CUL 7 GENE MUTATION 263238 1% 100% 1 Search CUL+7+GENE+MUTATION Search CUL+7+GENE+MUTATION

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 CLAYTON, PE , HANSON, D , MAGEE, L , MURRAY, PG , SAUNDERS, E , ABU-AMERO, SN , MOORE, GE , BLACK, GCM , (2012) EXPLORING THE SPECTRUM OF 3-M SYNDROME, A PRIMORDIAL SHORT STATURE DISORDER OF DISRUPTED UBIQUITINATION.CLINICAL ENDOCRINOLOGY. VOL. 77. ISSUE 3. P. 335-342 23 55% 17
2 HANSON, D , MURRAY, PG , BLACK, GCM , CLAYTON, PE , (2011) THE GENETICS OF 3-M SYNDROME: UNRAVELLING A POTENTIAL NEW REGULATORY GROWTH PATHWAY.HORMONE RESEARCH IN PAEDIATRICS. VOL. 76. ISSUE 6. P. 369-378 25 47% 10
3 DEMIR, K , ALTINCIK, A , BOBER, E , (2013) SEVERE SHORT STATURE DUE TO 3-M SYNDROME WITH A NOVEL OBSL1 GENE MUTATION.JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM. VOL. 26. ISSUE 1-2. P. 147-150 10 100% 1
4 HANSON, D , STEVENS, A , MURRAY, PG , BLACK, GCM , CLAYTON, PE , (2014) IDENTIFYING BIOLOGICAL PATHWAYS THAT UNDERLIE PRIMORDIAL SHORT STATURE USING NETWORK ANALYSIS.JOURNAL OF MOLECULAR ENDOCRINOLOGY. VOL. 52. ISSUE 3. P. 333 -344 18 51% 6
5 BADINA, A , PEJIN, Z , ODENT, T , BUZESCU, A , HUBER, C , CORMIER-DAIRE, V , GLORION, C , PANNIER, S , (2011) HIP DISLOCATION IN 3-M SYNDROME: RISK OF MISDIAGNOSIS.CLINICAL DYSMORPHOLOGY. VOL. 20. ISSUE 2. P. 114 -116 11 92% 1
6 LUGLI, L , BERTUCCI, E , MAZZA, V , ELMAKKY, A , FERRARI, F , NEUHAUS, C , PERCESEPE, A , (2016) PRE- AND POST-NATAL GROWTH IN TWO SISTERS WITH 3-M SYNDROME.EUROPEAN JOURNAL OF MEDICAL GENETICS. VOL. 59. ISSUE 4. P. 232 -236 9 100% 0
7 YAN, J , YAN, F , LI, ZJ , SINNOTT, B , CAPPELL, KM , YU, YB , MO, JY , DUNCAN, JA , CHEN, X , CORMIER-DAIRE, V , ET AL (2014) THE 3M COMPLEX MAINTAINS MICROTUBULE AND GENOME INTEGRITY.MOLECULAR CELL. VOL. 54. ISSUE 5. P. 791 -804 17 47% 15
8 HUBER, C , MUNNICH, A , CORMIER-DAIRE, V , (2011) THE 3M SYNDROME.BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM. VOL. 25. ISSUE 1. P. 143 -151 15 58% 13
9 KETTUNEN, KM , KARIKOSKI, R , HAMALAINEN, RH , TOIVONEN, TT , ANTONENKOV, VD , KULESSKAYA, N , VOIKAR, V , HOLTTA-VUORI, M , IKONEN, E , SAINIO, K , ET AL (2016) TRIM37-DEFICIENT MICE RECAPITULATE SEVERAL FEATURES OF THE MULTI-ORGAN DISORDER MULIBREY NANISM.BIOLOGY OPEN. VOL. 5. ISSUE 5. P. 584 -595 17 46% 0
10 AKAWI, NA , ALI, BR , HAMAMY, H , AL-HADIDY, A , AL-GAZALI, L , (2011) IS AUTOSOMAL RECESSIVE SILVER-RUSSEL SYNDROME A SEPARATE ENTITY OR IS IT PART OF THE 3-M SYNDROME SPECTRUM?.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 155A. ISSUE 6. P. 1236 -1245 14 54% 13

Classes with closest relation at Level 1


Rank Class id link
1 9078 NEDD8//COP9 SIGNALOSOME//NEDDYLATION
2 9519 SILVER RUSSELL SYNDROME//BECKWITH WIEDEMANN SYNDROME//UNIPARENTAL DISOMY
3 19492 FBXW7//FBW7//FBXO7
4 36588 PELGER HUET ANOMALY//PELGER HUET//PSEUDO PELGER HUET ANOMALY
5 18053 SECKEL SYNDROME//ASPM//MCPH1
6 10010 TRIM5 ALPHA//TRIM5//TRIMCYP
7 9853 ACHONDROPLASIA//HYPOCHONDROPLASIA//THANATOPHORIC DYSPLASIA
8 33110 MYHRE SYNDROME//GELEOPHYSIC DYSPLASIA//MICROSPHEROPHAKIA
9 37649 TRIAL BASED THOUGHT RECORD//TRIAL BASED COGNITIVE THERAPY//CORE BELIEF
10 15893 ELLIS VAN CREVELD SYNDROME//JEUNE SYNDROME//ORAL FACIAL DIGITAL SYNDROME

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