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Connection

Inderneel Sahai to Child

This is a "connection" page, showing publications Inderneel Sahai has written about Child.
Connection Strength

0.200
  1. Sahai I, Eaton RB, Hale JE, Mulcahy EA, Comeau AM. Long-term follow-up to ensure quality care of individuals diagnosed with newborn screening conditions: early experience in New England. Genet Med. 2010 Dec; 12(12 Suppl):S220-7.
    View in: PubMed
    Score: 0.043
  2. Roesch S, O'Sullivan A, Tschani S, Baghdasaryan A, Balasubramaniam S, Baric I, de Boer L, Gr?nert SC, Guzek A, Janssen M, Krumina Z, Koenig MK, Lewkowitz AM, Mochel F, Naldi AM, Plecko B, ?zt?rk K, O'Grady L, Riordan G, Rymen D, Sahai I, Santer R, Schiff M, Stettner GM, Tsiakas K, U?ar SK, Uzun ??, Weigel C, Witters P, Merkevicius K, Mayr JA, Wortmann SB, Iwanicka-Pronicka K. Hearing rehabilitation in SERAC1 related MEGD(H)EL syndrome - implications from a multi-center retrospective cohort study. Mol Genet Metab. 2025 Sep-Oct; 146(1-2):109193.
    View in: PubMed
    Score: 0.030
  3. Grady LO, Zoltick ES, Zouk H, He W, Perez E, Clarke L, Gold J, Strong A, Sahai I, Yeo J, Green RC, Karaa A, Gold NB. Long-Term Health Outcomes of Individuals With Pseudodeficiency Alleles in IDUA May Inform Newborn Screening Practices for Mucopolysaccharidosis Type I. Am J Med Genet A. 2025 Apr; 197(4):e63940.
    View in: PubMed
    Score: 0.029
  4. Ramirez Alcantara J, Grant NR, Sethuram S, Nagy A, Becker C, Sahai I, Stanley T, Halper A, Eichler FS. Early Detection of Adrenal Insufficiency: The Impact of Newborn Screening for Adrenoleukodystrophy. J Clin Endocrinol Metab. 2023 10 18; 108(11):e1306-e1315.
    View in: PubMed
    Score: 0.027
  5. Lucas AT, Lin AE, Cohen A, Mu?oz W, Kahle KT, Shin JH, Buch K, Sahai I, Carroll RW. Atlantoaxial instability associated with ALDH18A1 mutation. Am J Med Genet A. 2023 12; 191(12):2898-2902.
    View in: PubMed
    Score: 0.026
  6. Yuen L, Sahai I, O'Grady L, Selig M, Walker MA, Shah U, Misdraji J. Hepatic histologic findings in a case of MEGDHEL syndrome due to SERAC1 deficiency. Am J Med Genet A. 2022 09; 188(9):2760-2765.
    View in: PubMed
    Score: 0.024
  7. Mitchell ML, Hsu HW, Sahai I. The increased incidence of congenital hypothyroidism: fact or fancy? Clin Endocrinol (Oxf). 2011 Dec; 75(6):806-10.
    View in: PubMed
    Score: 0.012
  8. Bergmann AK, Sahai I, Falcone JF, Fleming J, Bagg A, Borgna-Pignati C, Casey R, Fabris L, Hexner E, Mathews L, Ribeiro ML, Wierenga KJ, Neufeld EJ. Thiamine-responsive megaloblastic anemia: identification of novel compound heterozygotes and mutation update. J Pediatr. 2009 Dec; 155(6):888-892.e1.
    View in: PubMed
    Score: 0.010
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.