Citation Impact
Citing Papers
Proliferation and functional maturation of Sertoli cells, and their relevance to disorders of testis function in adulthood
2003 Standout
Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54
2003 Standout
Comprehensive molecular portraits of human breast tumours
2012 StandoutNature
Bump-and-Hole Engineering Identifies Specific Substrates of Glycosyltransferases in Living Cells
2020 StandoutNobel
Genomic imprinting and dermatological disease
2006
The FGF family: biology, pathophysiology and therapy
2009 Standout
Control of mucin-type O-glycosylation: A classification of the polypeptide GalNAc-transferase gene family
2011
Cryptorchidism and hypospadias as a sign of testicular dysgenesis syndrome (TDS): Environmental connection
2010
Gi-Coupled GPCR Signaling Controls the Formation and Organization of Human Pluripotent Colonies
2009 StandoutNobel
Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome
1997
T-box genes in human disorders
2003
Glycopeptide-preferring Polypeptide GalNAc Transferase 10 (ppGalNAc T10), Involved in Mucin-type O-Glycosylation, Has a Unique GalNAc-O-Ser/Thr-binding Site in Its Catalytic Domain Not Found in ppGalNAc T1 or T2
2009 StandoutNobel
A Novel Transcription Factor, T-bet, Directs Th1 Lineage Commitment
2000 Standout
A Combined Analysis of Genomic and Primary Protein Structure Defines the Phylogenetic Relationship of New Members of the T-Box Family
1998 StandoutNobel
The mini-driver model of polygenic cancer evolution
2015 StandoutNobel
Diagnosis and Treatment of Primary Adrenal Insufficiency: An Endocrine Society Clinical Practice Guideline
2016 Standout
Biological roles of glycans
2016 Standout
Cleft lip and palate: understanding genetic and environmental influences
2011 Standout
Site-specific protein O-glycosylation modulates proprotein processing — Deciphering specific functions of the large polypeptide GalNAc-transferase gene family
2012
A homozygous missense mutation in human KLOTHO causes severe tumoral calcinosis
2007
Measuring the multifaceted roles of mucin-domain glycoproteins in cancer
2022 StandoutNobel
Differential expression of VegT and Antipodean protein isoforms in Xenopus
1999 StandoutNobel
Revealing the human mucinome
2022 StandoutNobel
Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family
1997 Standout
Fibroblast growth factor 23 is elevated before parathyroid hormone and phosphate in chronic kidney disease
2011 Standout
Monogenic Disorders of Puberty
2002
Evaluation of Factors Related to Late Recurrence - Later than 10 Years after the Initial Treatment - in Primary Breast Cancer
2013 Standout
Molecular genetic and biochemical analyses of FGF23 mutations in familial tumoral calcinosis
2008
A metabolic labeling approach for glycoproteomic analysis reveals altered glycoprotein expression upon GALNT3 knockdown in ovarian cancer cells
2016 StandoutNobel
Mammalian G Proteins and Their Cell Type Specific Functions
2005
GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5
2003 StandoutNature
Treatment of Cushing's Syndrome: An Endocrine Society Clinical Practice Guideline
2015
A Pragmatic Guide to Enrichment Strategies for Mass Spectrometry–Based Glycoproteomics
2020 StandoutNobel
Lectin Domains of Polypeptide GalNAc Transferases Exhibit Glycopeptide Binding Specificity
2011 StandoutNobel
Glycosylation in cancer: mechanisms and clinical implications
2015 Standout
Polypeptide GalNAc-transferase T3 and Familial Tumoral Calcinosis
2006
The Fibroblast Growth Factor signaling pathway
2015 Standout
Anatomical and Functional Aspects of Testicular Descent and Cryptorchidism*
1997
HIF-1α is required for development of the sympathetic nervous system
2019 StandoutNobel
EDC-2: The Endocrine Society's Second Scientific Statement on Endocrine-Disrupting Chemicals
2015 Standout
Hydrocortisone Dosing during Puberty in Patients with Classical Congenital Adrenal Hyperplasia: An Evidence-Based Recommendation
2009
Adipose-Derived Stem Cells for Regenerative Medicine
2007 Standout
Genetic Heterogeneity of Heart-Hand Syndromes
1995
ACC/AHA 2008 Guidelines for the Management of Adults With Congenital Heart Disease
2008 Standout
ACC/AHA 2008 Guidelines for the Management of Adults With Congenital Heart Disease: Executive Summary
2008 Standout
Isl1Cre reveals a common Bmp pathway in heart and limb development
2006
Engineering Orthogonal Polypeptide GalNAc-Transferase and UDP-Sugar Pairs
2019 StandoutNobel
The evolutionary biology of child health
2011
Management of adrenal incidentalomas: European Society of Endocrinology Clinical Practice Guideline in collaboration with the European Network for the Study of Adrenal Tumors
2016 Standout
Congenital Disorders of Glycosylation: A Rapidly Expanding Disease Family
2007
Works of R. Lala being referenced
Laparoscopic Unilateral Adrenalectomy in Children for Isolated Primary Pigmented Nodular Adrenocortical Disease (PPNAD): Case Report and Literature Review
2010
Heart‐hand syndrome II. A report of Tabatznik syndrome with new findings
1990
Possible relationship between ulnar‐mammary syndrome and split hand with aplasia of the ulna syndrome
1992
McCune-Albright Syndrome: A Clinical Longitudinal Study of 32 Patients
1999
Sperm Count of Young Men Surgically Treated for Cryptorchidism in the First and Second Year of Life: Fertility is Better in Children Treated at a Younger Age
2009
Familial tumoral calcinosis and testicular microlithiasis associated with a new mutation of GALNT3 in a white family
2006
Early medical and surgical treatment of cryptorchidism: clinical, anatomic, and histologic findings
1992
Auxological and biochemical parameters in assessing treatment of infants and toddlers with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
1993
Pubertal development in patients with McCune-Albright syndrome or pseudohypoparathyroidism.
2003